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Gamma Knife Radiosurgery in Gliomas: What Are They?

Glial cells in the brain or spinal cord are the source of gliomas, a form of tumor. The supporting cells of the nervous system, glial cells give neurones structure, defence, and nourishment. Roughly 80% of all malignant brain tumors and 30% of all brain tumors are gliomas.

The type of glial cell from which gliomas originate determines their classification:

Gliomas_ What Are They
Gliomas_ What Are They
  • (from astrocytes) Astrocytomas
  • (from oligodendrocytes) Oligodendrogliomas
  • From ependymal cells, ependymomas

Furthermore, gliomas are categorised by the World Health Organisation (WHO) into four categories (I to IV) according to how aggressive they appear under a microscope. High-grade gliomas (Grades III and IV) grow more quickly and are more invasive than low-grade gliomas (Grades I and II), which grow more slowly. The most frequent and aggressive malignant primary brain tumor is glioblastoma multiforme (GBM), a Grade IV glioma.

Do gliomas come in different types?

Based on the kind of glial cell they originate in, gliomas can be divided into three primary categories. Multiple cell types can be found in certain gliomas. These are known as mixed gliomas by medical professionals. Based on their growth rate and other characteristics, they classify each form of glioma as low-, mid-, or high-grade.

Do gliomas come in different types
Do gliomas come in different types

Among the gliomas are:

  1. Glioblastomas and diffuse intrinsic pontine gliomas (DIPGs) are examples of astrocytes: Astrocytes are the cells that give rise to these tumors. Astrocytomas that grow quickly or are extremely aggressive are called glioblastomas. In adults, they are the most prevalent malignant brain tumor. Children frequently develop gliomas called astrocytes. DIPG is an uncommon but extremely aggressive kind of childhood brain cancer. It primarily affects children and develops in the brain stem.
  2. Ependymomas: These tumors originate in glial cells called ependymocytes. Ependymomas typically develop in the brain’s or spinal cord ventricles. They do not spread outside of the brain or spine, but they may do so through the cerebrospinal fluid, which envelops and shields the brain and spinal cord. About 2% of all brain tumors are ependymomas. Children are more likely than adults to have them.
  3. Oligodendrogliomas: These tumors begin as oligodendrocytes, which are glial cells. Although oligodendrogliomas typically grow more slowly, they have the potential to become more aggressive over time. They hardly ever spread outside of the brain or spine, just like ependymomas. Adults are more likely than children to have them. One to two percent of all brain tumors are oligodendrogliomas.

Glioma symptoms

The location, size, and growth rate of the tumor all affect the symptoms of gliomas. Typical signs and symptoms include:

Glioma symptoms
Glioma symptoms
  • A headache
  • Seizures
  • Changes in personality or cognition
  • Issues with memory
  • Sensory abnormalities or motor weakness
  • Visual disruptions
  • Dizziness
  • Weakness or numbness on one side of the body
  • Difficulty in keeping balance and walking.
  • Vomiting & Nausea

Who is susceptible to gliomas?

Gliomas can happen to anyone, but the following things could make you more susceptible:

Who is susceptible to gliomas
Who is susceptible to gliomas
  • Age: Children under the age of twelve and older individuals over 65 are most likely to develop gliomas.
  • Ethnicity: Compared to other races, white people may be more susceptible to gliomas.
  • Family history: You may be more susceptible to gliomas if you have certain inherited genetic problems.
  • Sex: Men are slightly more likely than women to get gliomas.
  • Exposure to radiation or toxins: Prolonged or recurrent exposure to radiation or certain chemicals may raise your risk.

What is the frequency of gliomas?

In the United States, about 80,000 people receive a new primary brain tumor diagnosis every year. Gliomas make up about 25% of these.

Gliomas, especially those of the central nervous system (CNS), are seen in 5–10 out of every 100,000 people in India. About 2% of all malignant neoplasms in India are brain tumors, making up a sizable part of all brain tumors. Astrocytomas are a common kind of glioma, which can occur in both children and adults.

Why do gliomas occur or what is the cause?

According to research, gliomas and other brain and spinal cord tumors are caused by alterations in DNA. DNA is found in our genes. They guide cells on how to divide and multiply. Cells can proliferate uncontrollably if our genes’ DNA undergoes mutations.

Parents may pass on genetic mutations to you. They can also happen all at once while you’re alive.

What side effects might gliomas cause/complications?

The following are glioma complications that could be fatal:

  • Bleeding in the brain, or brain haemorrhage.
  • A brain herniation occurs when brain tissue shifts from its typical location within the skull.
  • Hydrocephalus, or accumulation of fluid in the brain.
  • Pressure within your head.
  • Seizures.

How can gliomas be identified or diagnosed?

In addition to reviewing your medical history, your healthcare professional assesses your symptoms. A thorough neurological and physical examination will also be performed.

The most popular imaging tests for brain tumors are MRIs and CT scans. In addition to other tumors in your body, your doctor searches for brain tumors.

Doctor will perform a biopsy if your imaging scans reveal an abnormal lump. The process of analysing a tissue sample is called a biopsy. The biopsy will assist them in figuring out:

  • If the growth is malignant.
  • If an aberrant gene is the cause of the tumor.
  • The tumor’s cell structure.
  • The tumor’s grade, or aggressiveness.

Care and Therapy

How do you cure a glioma?

The following variables will affect your glioma treatment plan:

  • If you have already had treatment for brain cancer.
  • The tumor’s size, type, and location.
  • Your age.
  • Your well-being.

Surgery is typically the first course of treatment for gliomas. If the tumor is easily accessible, a surgeon might be able to remove it altogether. However, gliomas can be challenging to fully eradicate, particularly if they are in close proximity to sensitive brain regions or are difficult to reach.

Surgery should be followed by other therapies like radiation therapy and chemotherapy. These are adjuvant therapy, which means that following surgery, they eliminate any cancer cells or tumor components that may still be present. However, your doctor may employ radiation therapy or chemotherapy as your main therapies if a tumor cannot be removed.

Operation/Surgery

The most popular procedure for glioma removal is an open brain surgery called a craniotomy. You might be a candidate for laser ablation, depending on the tumor’s size and location. In this minimally invasive procedure, a brain tumor can be completely or partially destroyed using laser heat.

To guide the procedure, a surgeon may employ specialised methods like brain mapping or imaging. Brain mapping reveals the parts of your brain that regulate essential processes. By knowing this, your surgeon can prevent damaging or destroying vital brain tissue.

Radiation

Strong radiation doses are used in radiation therapy to eradicate tumors. For gliomas, your doctor might suggest radiation treatment. By precisely targeting the tumor’s form, radiation therapy reduces the possibility of harming nearby tissues.

Brachytherapy is another type of radiation treatment that you could get. To treat a tumor, a medical professional utilises radiation sources near the tumor. Radiation is released from the sources without damaging surrounding tissues.

Chemotherapy

Chemotherapy is the process of killing cancer cells with chemicals. It cures a variety of cancers. This treatment can be administered directly or orally.

One frequent chemotherapeutic medication used to increase the effectiveness of radiation therapy is temozolomide.

Avoidance/Prevention

How can gliomas be avoided?

The majority of glioma risk factors, including age and race, are uncontrollable. However, the evolution of low-grade gliomas into high-grade gliomas may be slowed or stopped by early detection and treatment. You might wish to think about genetic testing if brain tumors run in your family. Discuss the advantages and disadvantages of genetic testing with a genetic counsellor or your healthcare provider.

Additionally, it is wise to:

  • Don’t expose your head to too much radiation.
  • Keeping up a healthy way of living.

Prognosis and Outlook

What is the prognosis for glioma patients?

Glioma survival rates differ depending on the kind, grade, and age of the tumor. The prognosis may also be impacted by specific mutations. The prognosis is poorer for those who are diagnosed and treated later in life. Adults and children with low-grade ependymomas, oligodendrogliomas, and astrocytomas have the highest five-year survival rates. For glioblastomas, it is the lowest (between 6% and 20%).

Glioma Gamma Knife Radiosurgery

Glioma Gamma Knife Radiosurgery
Glioma Gamma Knife Radiosurgery

A type of stereotactic radiosurgery (SRS) called “gamma knife” uses intensely concentrated radiation beams to target the tumor while exposing the least amount of healthy brain tissue possible. It is especially helpful for gliomas that are in sensitive brain regions or are difficult to physically approach.

Radiosurgery with Gamma Knife for Low-Grade Gliomas

Gamma Knife radiosurgery provides a less invasive treatment option for low-grade gliomas (WHO Grade I and II) that can:

  • After partial resection, control the growth of any remaining tumor.
  • Treat well-defined, tiny lesions without requiring open surgery.
  • Preserve neurocognitive function by delaying or minimising the need for whole-brain radiation.

Research has demonstrated that Gamma Knife can successfully treat low-grade gliomas with few adverse effects, providing long-lasting local control and enhanced quality of life. Younger patients or those with tumors in functionally sensitive areas benefit most from it.

Radiosurgery with Gamma Knife for High-Grade Gliomas

Treatment for high-grade gliomas, such as glioblastoma multiforme (GBM), is difficult and aggressive. Uses for Gamma Knife radiosurgery include:

  1. Recurrent High-Grade Gliomas: Used as a salvage treatment when tumors return following initial chemotherapy, radiation, and surgery.
  2. Targeting isolated or satellite lesions that are not responsive to additional surgical procedures is the goal of small residual or metastatic lesions.

In certain situations, Gamma Knife can effectively control tumors, extending survival and improving quality of life, however it should not be used in place of conventional treatment methods. To maximise results, multidisciplinary planning and careful patient selection are essential.

Gamma Knife Radiosurgery Benefits

Gamma Knife Stereotactic Radiosurgery
Gamma Knife Stereotactic Radiosurgery
  • Precision: Accurately targets tumors within millimetres.
  • Safety: Reduces the amount of radiation that reaches healthy brain tissue.
  • Convenience: A short recovery period following an outpatient treatment.
  • Repeatability: For recurrent tumors, it is possible to repeat if required.

In conclusion

Glioma treatment necessitates a customised, interdisciplinary strategy that strikes a balance between tumor control and neurological function preservation. A potent weapon in this arsenal is Gamma Knife radiosurgery, which gives patients with both low-grade and high-grade gliomas hope and better results.

For the best outcome, it is essential to speak with a skilled neurosurgeon who can explain the various treatment choices, including cutting-edge methods like Gamma Knife radiosurgery, if you or a loved one has been diagnosed with a glioma.

Sources:

  1. https://pmc.ncbi.nlm.nih.gov/articles/PMC4991137/
  2. https://www.ncbi.nlm.nih.gov/books/NBK441874/
  3. https://www.ncbi.nlm.nih.gov/books/NBK441874/#_article-18547_s13_
  4. https://my.clevelandclinic.org/health/diseases/21969-glioma
  5. https://www.mayoclinic.org/diseases-conditions/glioma/symptoms-causes/syc-20350251
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  8. https://www.hopkinsmedicine.org/health/conditions-and-diseases/gliomas
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Gamma Knife Radiosurgery for Trigeminal Neuralgia

The trigeminal nerve, one of the most extensively distributed nerves in the brain, is impacted by Trigeminal Neuralgia (TN), also referred to as tic douloureux, a chronic pain disorder. Trigeminal neuralgia, which is characterised by sudden, intense facial pain that resembles an electric shock, can be emotionally and physically incapacitating. Excruciating pain can be triggered by even minor facial stimulation, like cleaning your teeth or applying cosmetics.

Trigeminal Neuralgia
Trigeminal Neuralgia

This disorder usually affects one side of the face, usually the jaw and lower face, though it can also occasionally affect the area above the eye and around the nose.

Trigeminal Neuralgia Causes

Trigeminal Neuralgia Causes
Trigeminal Neuralgia Causes

Compression of the trigeminal nerve, frequently by a blood vessel like the superior cerebellar artery, is the main cause of trigeminal neuralgia. Pain signals are failed as a result of this pressure because it destroys the myelin sheath that protects the nerve.

Other less frequent reasons are as follows:

  1. Multiple sclerosis, which also causes myelin damage
  2. Trigeminal nerve tumors pushing on it
  3. Anomalies or lesions in the brain
  4. Trauma or stroke that damages the nerve

Trigeminal Neuralgia Symptoms

Symptoms could consist of:

  • Facial pain that is sudden, intense, stabbing, or shock-like
  • Periods of pain that range in duration from a few seconds to many minutes
  • Regular actions such as speaking, chewing, or touching the face might cause this.
  • Usually, one side of the face has pain.
  • If treatment is not received, episodes gradually increase in frequency and Intensity.

Accurate diagnosis is essential since trigeminal neuralgia is frequently misdiagnosed as migraines, dental issues, or temporomandibular joint (TMJ) abnormalities.

Diagnosis

Trigeminal neuralgia is typically diagnosed based on:

  • Medical background and symptom description
  • Examining the nervous system to identify any involvement
  • MRI scans to check for vascular compression and rule out tumours or multiple sclerosis

Options for Treatment

  1. Medications

Anticonvulsant medications like these are typically used as the first line of treatment.

  • Tegretol, or carbamazepine
  • Oxcarbazepine
  • Pregabalin or Gabapentin

These drugs decrease or cease the nerve’s capacity to transmit pain signals, but they may have negative side effects and lose their effectiveness over time.

  1. Surgical Procedures

Several surgical methods may be taken into consideration when drugs don’t work or side effects become unbearable:

  • MDV, or microvascular decompression

Include shifting or excising blood vessels that are putting pressure on the nerve. This is regarded as a very successful long-term fix.

  • Rhizotomy

A technique that reduces pain that harms nerve fibres. Among the methods are glycerol injection, balloon compression, and radiofrequency thermal lesioning.

Radiosurgery with Gamma Knife for Trigeminal Neuralgia

Radiosurgery with Gamma Knife for Trigeminal Neuralgia
Radiosurgery with Gamma Knife for Trigeminal Neuralgia

Gamma Knife Radiosurgery: What is it?

A cutting-edge, non-invasive method of radiation treatment called Gamma Knife Radiosurgery targets the trigeminal nerve root with intensely concentrated radiation beams. This technique is usually done as an outpatient and doesn’t require any incisions.

How Does It Operate?

  • The exact location of high-dose radiation is the trigeminal nerve’s exit from the brainstem.
  • The transmission of pain signals is disrupted by the radiation’s destruction to the nerve fibres.
  • Usually, pain subsides gradually over a period of weeks to months.

Gamma Knife Radiosurgery Advantages

Gamma Knife Stereotactic Radiosurgery
Gamma Knife Stereotactic Radiosurgery
  • Non-invasive: No anaesthesia or incisions are necessary.
  • Safe: Very little chance of infection or other problems
  • Effective: 70–90% of individuals experience long-term pain relief
  • Fast recovery: Within a day, the majority of patients resume their regular activities.

Who’s the candidate or the patient?

  • Responded to or are unable to take medicine
  • They are too old or have health issues to be good candidates for standard surgery.
  • Trigeminal neuralgia that returns after prior operations

Coping with Trigeminal Pain

Although trigeminal neuralgia can be very difficult to live with, there are effective therapies for it. Quality of life can be considerably enhanced by early diagnosis and the proper medical, surgical, or radiosurgical treatments. A possible non-invasive substitute for open surgery that provides long-term pain relief is Gamma Knife Radiosurgery.

In conclusion

Although trigeminal neuralgia is a complicated disorder, it is curable. Seeking advice from a neurosurgeon experienced in treating facial pain issues is crucial if you or a loved one is suffering from severe, unexpected facial pain.

Sources:

  1. https://www.ninds.nih.gov/health-information/disorders/trigeminal-neuralgia
  2. https://www.ncbi.nlm.nih.gov/books/NBK554486/
  3. https://pmc.ncbi.nlm.nih.gov/articles/PMC9489081/
  4. https://pmc.ncbi.nlm.nih.gov/articles/PMC9452385/
  5. https://jkns.or.kr/upload/pdf/jkns-2021-0303.pdf
  6. https://jamanetwork.com/journals/jamaneurology/fullarticle/774556
  7. https://www.neurosurgery.pitt.edu/centers/image-guided-neurosurgery/trigeminal-neuralgia
  8. https://www.nature.com/articles/s41572-024-00523-z
  9. https://www.aans.org/patients/conditions-treatments/trigeminal-neuralgia/
  10. https://neurosurgery.ucsf.edu/trigeminal-neuralgia-faq

Gamma Knife Radiosurgery for Hypothalamic Hamartomas

The hypothalamus, a region at the base of the brain that is essential for many autonomic processes, including temperature regulation, hunger, thirst, emotional responses, and hormone production through the pituitary gland, is the site of a rare, benign (non-cancerous) brain lesion known as a hypothalamic hamartoma (HH).

Hypothalamic Hamartoma: What Is It?

Hypothalamic Hamartoma_ What Is It
Hypothalamic Hamartoma_ What Is It

Depending on their size, location, and proximity to adjacent brain regions, HHs can have a major impact on neurological and endocrine function even though they are not malignant.

Deep inside your brain is a structure the size of an almond called the hypothalamus. In order for your body’s systems to operate as intended, it connects your endocrine and neurological systems to preserve homeostasis, or a state of equilibrium.

The growth is a tumour that is not malignant. It can interfere with a number of crucial hypothalamic processes, such as:

crucial hypothalamic processes
crucial hypothalamic processes
  • Blood pressure
  • Body temperature
  • Stress-related emotions, hunger, and thirst
  • Hormone release from the pituitary gland
  • Sleep and wakefulness cycles

As a foetus grows, a hypothalamic hamartoma arises. As your brain develops, so does it. No other areas of your body or brain are affected by HH. One lesion is often involved, although occasionally there are many.

HH symptoms can be managed using a variety of treatment approaches.

Which kinds of hypothalamic hamartomas are there?

Which kinds of hypothalamic hamartomas are there
Which kinds of hypothalamic hamartomas are there

Based on their location and the symptoms they produce, hypothalamic hamartomas can be divided into two categories:

  1. Lesion inside the hypothalamus. There is a growth close to the rear of your hypothalamus. It may cause seizures and aberrant behaviour by interfering with the electrical activity in your brain.
  2. Lesion of the parahypothalamus (pedunculated lesion). Your hypothalamus has a growth close to its front. Early puberty could result from it.

It’s possible to have both kinds at the same time.

Clinical Display

  1. Gelastic Seizures

Gelastic seizures, which are typified by unexpected, inappropriate bursts of laughter, are one of the main symptoms of HH. These seizures frequently start in early childhood or infancy, and at first they could be mistaken for behavioural problems.

  1. Additional Seizures

People may get drop attacks, tonic-clonic seizures, or complex partial seizures as the illness worsens. Over time, these seizures may develop resistant to treatment.

  1. Behavioural and Cognitive Problems

Cognitive delays, hyperactivity, anger, mood swings, and other behavioural issues are common in children with HH. These are believed to be secondary to hypothalamic dysfunction and continuous seizure activity.

Causes and Symptoms

Causes and Symptoms
Causes and Symptoms

What signs or symptoms of hypothalamic hamartoma are present?

Although they differ from person to person, hypothalamic hamartoma symptoms might include:

  • Early or premature puberty
  • Seizures
  • Symptoms related to the nervous system

Hypothalamic hamartoma: what causes it?

There is no known way to avoid HH, and experts are unsure of its specific cause. Most of the cases occur at random. This indicates that you probably won’t inherit it because they don’t typically run in your biological family history.

A somatic mutation of the GLI3 gene was discovered within the tumour in recent investigations of excised tumour tissue. Tumour tissue that has been removed has also revealed further genetic variations. To find out more about the potential genetics involved, research is still ongoing.

Pallister-Hall syndrome (PHS), a hereditary disorder, may be connected to hypothalamic hamartoma. A genetic variation that can lead to anomalies in the development of your hands, feet, larynx (voice box), and anus is the source of this condition.

How is a diagnosis of hypothalamic hamartoma made?

To diagnose HH, doctor will recommend imaging testing. An MRI produces incredibly very fine pictures of your brain. For children to remain motionless during an MRI, little sedation is typically required. The visuals may get blurry if they move.

If you suffer seizures, your doctor might also suggest an electroencephalogram (EEG). Brain’s electrical activity is tracked by this test.

The degree of cognitive issues, including those related to thinking, learning, and memory, can be assessed through neurological testing. In order to measure hormone levels, your doctor might also suggest blood testing. Treatment may be guided by these tests.

The symptoms of HH might mimic those of other neurological disorders, making diagnosis challenging.

Classification

HHs are frequently categorised according to where they attach and where they lie in relation to the third ventricle and hypothalamus:

  • Pedunculated: Affixed to the third ventricle’s floor by a stalk.
  • Sessile: Widely distributed connection that frequently infiltrates the hypothalamus directly.

Options for Treatment

Options for Treatment
Options for Treatment
  1. Health Care Administration

  • HH patients frequently have drug-resistant seizures, despite the fact that antiepileptic medications (AEDs) are typically the first line of treatment.
  1. The use of surgery

  • Although open resection of the lesion has been tried in the past, there is a substantial risk of morbidity because of its deep placement and close proximity to important brain regions.
  1. Options That Are Not Too Invasive

  • The process of cutting seizure pathways is known as endoscopic disconnection.
  • A more recent technique that uses image-guided thermal ablation is laser interstitial thermal treatment (LITT).

Radiosurgery with Gamma Knife for Hypothalamic Hamartomas

Gamma Knife Radiosurgery: What is it?

Radiosurgery with Gamma Knife for Hypothalamic Hamartomas
Radiosurgery with Gamma Knife for Hypothalamic Hamartomas

Without requiring open surgery, Gamma Knife radiosurgery is a non-invasive, stereotactic radiosurgical procedure that accurately targets aberrant brain tissue using concentrated gamma radiation beams.

Function in Hamartomas of the Hypothalamus

For patients with HH, gamma knife radiosurgery has become a safe and efficient therapy option, particularly for those with inoperable lesions or those who are not good candidates for surgery.

Advantages

  • Non-invasive: No craniotomy or incisions are needed.
  • High precision: Reduces the amount of radiation that reaches nearby healthy tissues.
  • Low risk: Less likely to cause problems than open surgery.
  • One session is frequently required for an outpatient operation.

Efficiency

  • Notable decrease in seizures, particularly gelastic seizures.
  • Improvement in post-treatment behaviour and cognitive abilities.
  • Multiple sessions or additional therapy may be necessary for certain patients.

Limitations and Risks

Limitations and Risks
Limitations and Risks
  • Delayed response: After treatment, seizure control may take weeks or months.
  • Depending on radiation dosage and lesion size, there is a rare chance of hormone imbalance or neurocognitive consequences.

Prognosis and Follow-Up
After therapy, patients need:

  • Routine endocrinological and neurological assessments.
  • MRI scans performed in succession to track lesion growth and response.
  • Neuropsychological evaluations, particularly in children.

The prognosis varies according to:

  • Age of onset
  • Frequency of seizures
  • The method of treatment used
  • Reaction to treatment

Many patients might see notable changes in their behaviour, quality of life, and seizure control with the right kind of care.

In conclusion

Despite being uncommon and benign, hypothalamic hamartomas can cause crippling neurological and hormonal problems, particularly in young patients. Timely treatment and accurate diagnosis are essential. Gamma Knife radiosurgery is a safe, minimally invasive, and successful method of treating medically refractory seizures brought on by HH among the developing therapy alternatives.

For appropriate assessment and treatment, see a neurosurgeon if you or a loved one is exhibiting odd laughter fits, seizures, or early puberty symptoms.

Sources:

  1. https://www.ncbi.nlm.nih.gov/books/NBK560663/
  2. https://radiopaedia.org/articles/hypothalamic-hamartoma
  3. https://www.epilepsy.com/causes/structural/hypothalamic-hamartoma
  4. https://pmc.ncbi.nlm.nih.gov/articles/PMC8610628/
  5. https://rarediseases.org/rare-diseases/hypothalamic-hamartoma/
  6. https://www.sciencedirect.com/science/article/abs/pii/S1090379816300605#:~:text=The%20Gamma%2Dknife%20technique%20is%20a%20safe%20and%20effective%20option,and%2For%20serious%20behavioral%20disorders.
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  8. https://pubmed.ncbi.nlm.nih.gov/21121804/
  9. https://thejns.org/view/journals/j-neurosurg/102/Special_Supplement/article-p53.xml
  10. https://www.sciencedirect.com/science/article/abs/pii/S1071909107000241

Gamma-Knife Radiosurgery in Juvenile Nasopharyngeal Angiofibroma

A rare, benign, but locally aggressive vascular tumor that develops in the nasopharynx, juvenile nasopharyngeal angiofibroma (JNA) mostly affects teenage boys. By destroying nearby tissues and structures, it can act aggressively even though it is histologically benign (non-cancerous). It is essential for patients and physicians to comprehend the nature of JNA, its presentation, diagnosis, and available treatments, including cutting-edge methods like Gamma Knife Radiosurgery.

What is it?

Juvenile Nasopharyngeal Angiofibroma
Juvenile Nasopharyngeal Angiofibroma

The fibrovascular tumor known as JNA typically begins close to the sphenopalatine foramen, which is situated at the rear of the nasal cavity. Despite being benign, the tumor is well-known for its propensity to bleed heavily, both naturally and during surgery, because of its abundant blood supply.

The study of epidemiology

The study of epidemiology_ Juvenile Nasopharyngeal Angiofibroma
The study of epidemiology_ Juvenile Nasopharyngeal Angiofibroma
  • Age group: Boys between the ages of 10 and 25 are most frequently observed.
  • Gender: It almost primarily impacts men.
  • Less than 0.05% of all head and neck tumors are caused by this tumor.

Causes and Symptoms

Early signs and symptoms include:

Causes and Symptoms_ Juvenile Nasopharyngeal Angiofibroma
Causes and Symptoms_ Juvenile Nasopharyngeal Angiofibroma
  • Nosebleeds that are severe or frequent
  • Congestion of the nose
  • Runny nose

As the tumor grows, the symptoms worsen. More severe symptoms may include:

  • Swelling in your face, particularly in your cheeks
  • Pain
  • Eyes that are watery
  • Eyes that bulge and eyelids that droop
  • Headaches
  • Vision loss
  • Double vision
  • Loss of hearing
  • Problems with speech
  • Apnoea during sleep
  • Numbness in the face

It is caused by what?

The reasons for JNA are not entirely understood by experts. Hormones are probably involved because these tumors almost exclusively affect men. According to experts, JNA tumors are not inherited.

Risk factors for juvenile nasopharyngeal angiofibroma

For JNA, there aren’t many distinct risk factors. Although JNA is not inherited, you are at a higher risk of developing it if any members of your biological family have familial adenomatous polyposis (FAP), a rare disorder in which precancerous polyps develop in your large intestine. This relationship is still being investigated by experts.

What side effects might juvenile nasopharyngeal angiofibroma cause?

If untreated, can result in:

  • Having trouble breathing
  • Speech, hearing, and vision problems
  • Deformities of the face, such drooping eyelids or protruding eyes
  • Anosmia is the loss of smell
  • Severe blood loss and nosebleeds
  • Shift in mental condition

How is angiofibroma of the juvenile nasopharynx diagnosed?

During an examination, a medical professional can make the diagnosis of JNA. They will examine your nose and then enquire about your symptoms. For additional testing, they can also recommend that you see an otolaryngologist (ENT).

Which diagnostic procedures can be used to identify juvenile nasopharyngeal angiofibroma?

Your doctor will want to perform imaging testing if they suspect JNA. These could consist of:

  • Computed tomography, or CT, scans.
  • Magnetic resonance imaging, or MRI.
  • Scans using PET (positron emission tomography).

To examine the tumor, they might also undertake a nasal endoscopy. A light and camera are attached at the end of an endoscope, which is a long, flexible tube. To view within your nasal cavity, a healthcare professional will carefully insert an endoscope into your nose. You should not experience discomfort since they will apply a numbing spray, which will cause pressure.

What is the course of treatment for juvenile nasopharyngeal angiofibroma?

  • The recommended treatment for juvenile nasopharyngeal angiofibroma is surgery. Radiation therapy is also necessary for some people.
  • The location and size of the JNA tumor determine the course of treatment.

Surgery for nasopharyngeal angiofibroma in children

The entire JNA tumor is intended to be removed during surgery. A surgeon may be able to remove the tumor through your nose (endoscopic surgery), depending on its size and location. This procedure will be carried out in a hospital by an otolaryngologist.

Radiation treatment for JNA

Because of its placement, surgeons may not be able to remove the entire tumor in some circumstances. Your doctor might suggest radiation treatment or additional surgery if the tumor cannot be removed or if it returns after surgery. High-energy X-ray beams are used in this treatment to reduce the tumor’s size.

For prevention, there is no known way to prevent JNA tumors.

Gamma-Knife Radiosurgery for Nasopharyngeal Angiofibroma in Children

A non-invasive, extremely accurate type of radiation therapy called Gamma Knife Radiosurgery (GKRS) targets the tumor with concentrated radiation while preserving nearby healthy tissues. It is a promising complement or substitute for surgery in the treatment of JNA, especially when the tumor has intracranial extension or surgery is not practical.

Gamma Knife Indications in JNA:

  • Remaining tumor after surgery
  • Recurrence following surgery
  • Tumors involving the deep base of the skull or the brain
  • Individuals who are not good candidates for surgery

Gamma Knife Radiosurgery Benefits:

  • Minimally invasive—no incision during surgery is necessary
  • Targeting the tumor with high precision while preserving important surrounding structures
  • Reduced likelihood of problems
  • An outpatient surgery that requires little recovery time
  • Outstanding rates of tumor control in long-term monitoring studies

Results:

Research shows tumor control rates of between 85 and 90 percent, with tumors gradually regressing over several months. When surgery is not enough to treat symptoms like nasal blockage and epistaxis, GKRS has been proven successful.

Diagnosis and Monitoring

The majority of patients have outstanding long-term results when they receive the right care. Monitoring for recurrence requires routine imaging follow-up, particularly in the initial years after therapy. MRI scans are advised periodically for patients receiving Gamma Knife treatment in order to evaluate tumor regression.

In conclusion

A difficult but treatable disorder is juvenile nasopharyngeal angiofibroma. Although surgical resection is still the mainstay of treatment, Gamma Knife Radiosurgery has become a useful method for treating inoperable or residual tumors because it provides great control with little morbidity.

To create the optimal treatment plan for every patient, a multidisciplinary team of radiation oncologists, neurosurgeons, ENT specialists, and interventional radiologists is required.

Source:

  1. https://www.ncbi.nlm.nih.gov/books/NBK545240/
  2. https://pmc.ncbi.nlm.nih.gov/articles/PMC4989574/
  3. https://radiopaedia.org/articles/juvenile-nasopharyngeal-angiofibroma
  4. https://www.childrenshospital.org/conditions/juvenile-nasopharyngeal-angiofibroma#:~:text=What%20is%20juvenile%20nasopharyngeal%20angiofibroma,can%20expand%20quickly%20and%20extensively.
  5. https://emedicine.medscape.com/article/872580-overview?form=fpf
  6. https://journals.lww.com/neur/fulltext/2021/69050/adjuvant_gamma_knife_radiosurgery_for_advanced.62.aspx#:~:text=To%20conclude%2C%20GKRS%20is%20a,50%25%20isodose)%20marginal%20dose.
  7. https://pmc.ncbi.nlm.nih.gov/articles/PMC2729909/
  8. https://pubmed.ncbi.nlm.nih.gov/16891831/
  9. https://www.thieme-connect.com/products/ejournals/pdf/10.1055/s-0043-1777293.pdf
  10. https://www.ejgm.co.uk/download/juvenile-nasopharyngeal-angiofibroma-6819.pdf

Gamma-Knife Radiosurgery in Juvenile Nasopharyngeal Angiofibroma

A rare, benign, but locally aggressive vascular tumor that develops in the nasopharynx, juvenile nasopharyngeal angiofibroma (JNA) mostly affects teenage boys. By destroying nearby tissues and structures, it can act aggressively even though it is histologically benign (non-cancerous). It is essential for patients and physicians to comprehend the nature of JNA, its presentation, diagnosis, and available treatments, including cutting-edge methods like Gamma Knife Radiosurgery.

What is it?

Juvenile Nasopharyngeal Angiofibroma
Juvenile Nasopharyngeal Angiofibroma

The fibrovascular tumor known as JNA typically begins close to the sphenopalatine foramen, which is situated at the rear of the nasal cavity. Despite being benign, the tumor is well-known for its propensity to bleed heavily, both naturally and during surgery, because of its abundant blood supply.

The study of epidemiology

The study of epidemiology_ Juvenile Nasopharyngeal Angiofibroma
The study of epidemiology_ Juvenile Nasopharyngeal Angiofibroma
  • Age group: Boys between the ages of 10 and 25 are most frequently observed.
  • Gender: It almost primarily impacts men.
  • Less than 0.05% of all head and neck tumors are caused by this tumor.

Causes and Symptoms

Early signs and symptoms include:

Causes and Symptoms_ Juvenile Nasopharyngeal Angiofibroma
Causes and Symptoms_ Juvenile Nasopharyngeal Angiofibroma
  • Nosebleeds that are severe or frequent
  • Congestion of the nose
  • Runny nose

As the tumor grows, the symptoms worsen. More severe symptoms may include:

  • Swelling in your face, particularly in your cheeks
  • Pain
  • Eyes that are watery
  • Eyes that bulge and eyelids that droop
  • Headaches
  • Vision loss
  • Double vision
  • Loss of hearing
  • Problems with speech
  • Apnoea during sleep
  • Numbness in the face

It is caused by what?

The reasons for JNA are not entirely understood by experts. Hormones are probably involved because these tumors almost exclusively affect men. According to experts, JNA tumors are not inherited.

Risk factors for juvenile nasopharyngeal angiofibroma

For JNA, there aren’t many distinct risk factors. Although JNA is not inherited, you are at a higher risk of developing it if any members of your biological family have familial adenomatous polyposis (FAP), a rare disorder in which precancerous polyps develop in your large intestine. This relationship is still being investigated by experts.

What side effects might juvenile nasopharyngeal angiofibroma cause?

If untreated, can result in:

  • Having trouble breathing
  • Speech, hearing, and vision problems
  • Deformities of the face, such drooping eyelids or protruding eyes
  • Anosmia is the loss of smell
  • Severe blood loss and nosebleeds
  • Shift in mental condition

How is angiofibroma of the juvenile nasopharynx diagnosed?

During an examination, a medical professional can make the diagnosis of JNA. They will examine your nose and then enquire about your symptoms. For additional testing, they can also recommend that you see an otolaryngologist (ENT).

Which diagnostic procedures can be used to identify juvenile nasopharyngeal angiofibroma?

Your doctor will want to perform imaging testing if they suspect JNA. These could consist of:

  • Computed tomography, or CT, scans.
  • Magnetic resonance imaging, or MRI.
  • Scans using PET (positron emission tomography).

To examine the tumor, they might also undertake a nasal endoscopy. A light and camera are attached at the end of an endoscope, which is a long, flexible tube. To view within your nasal cavity, a healthcare professional will carefully insert an endoscope into your nose. You should not experience discomfort since they will apply a numbing spray, which will cause pressure.

What is the course of treatment for juvenile nasopharyngeal angiofibroma?

  • The recommended treatment for juvenile nasopharyngeal angiofibroma is surgery. Radiation therapy is also necessary for some people.
  • The location and size of the JNA tumor determine the course of treatment.

Surgery for nasopharyngeal angiofibroma in children

The entire JNA tumor is intended to be removed during surgery. A surgeon may be able to remove the tumor through your nose (endoscopic surgery), depending on its size and location. This procedure will be carried out in a hospital by an otolaryngologist.

Radiation treatment for JNA

Because of its placement, surgeons may not be able to remove the entire tumor in some circumstances. Your doctor might suggest radiation treatment or additional surgery if the tumor cannot be removed or if it returns after surgery. High-energy X-ray beams are used in this treatment to reduce the tumor’s size.

For prevention, there is no known way to prevent JNA tumors.

Gamma-Knife Radiosurgery for Nasopharyngeal Angiofibroma in Children

A non-invasive, extremely accurate type of radiation therapy called Gamma Knife Radiosurgery (GKRS) targets the tumor with concentrated radiation while preserving nearby healthy tissues. It is a promising complement or substitute for surgery in the treatment of JNA, especially when the tumor has intracranial extension or surgery is not practical.

Gamma Knife Indications in JNA:

  • Remaining tumor after surgery
  • Recurrence following surgery
  • Tumors involving the deep base of the skull or the brain
  • Individuals who are not good candidates for surgery

Gamma Knife Radiosurgery Benefits:

  • Minimally invasive—no incision during surgery is necessary
  • Targeting the tumor with high precision while preserving important surrounding structures
  • Reduced likelihood of problems
  • An outpatient surgery that requires little recovery time
  • Outstanding rates of tumor control in long-term monitoring studies

Results:

Research shows tumor control rates of between 85 and 90 percent, with tumors gradually regressing over several months. When surgery is not enough to treat symptoms like nasal blockage and epistaxis, GKRS has been proven successful.

Diagnosis and Monitoring

The majority of patients have outstanding long-term results when they receive the right care. Monitoring for recurrence requires routine imaging follow-up, particularly in the initial years after therapy. MRI scans are advised periodically for patients receiving Gamma Knife treatment in order to evaluate tumor regression.

In conclusion

A difficult but treatable disorder is juvenile nasopharyngeal angiofibroma. Although surgical resection is still the mainstay of treatment, Gamma Knife Radiosurgery has become a useful method for treating inoperable or residual tumors because it provides great control with little morbidity.

To create the optimal treatment plan for every patient, a multidisciplinary team of radiation oncologists, neurosurgeons, ENT specialists, and interventional radiologists is required.

Source:

  1. https://www.ncbi.nlm.nih.gov/books/NBK545240/
  2. https://pmc.ncbi.nlm.nih.gov/articles/PMC4989574/
  3. https://radiopaedia.org/articles/juvenile-nasopharyngeal-angiofibroma
  4. https://www.childrenshospital.org/conditions/juvenile-nasopharyngeal-angiofibroma#:~:text=What%20is%20juvenile%20nasopharyngeal%20angiofibroma,can%20expand%20quickly%20and%20extensively.
  5. https://emedicine.medscape.com/article/872580-overview?form=fpf
  6. https://journals.lww.com/neur/fulltext/2021/69050/adjuvant_gamma_knife_radiosurgery_for_advanced.62.aspx#:~:text=To%20conclude%2C%20GKRS%20is%20a,50%25%20isodose)%20marginal%20dose.
  7. https://pmc.ncbi.nlm.nih.gov/articles/PMC2729909/
  8. https://pubmed.ncbi.nlm.nih.gov/16891831/
  9. https://www.thieme-connect.com/products/ejournals/pdf/10.1055/s-0043-1777293.pdf
  10. https://www.ejgm.co.uk/download/juvenile-nasopharyngeal-angiofibroma-6819.pdf

Gamma Knife Radiosurgery in Obsessive Compulsive Disorder (OCD)

A chronic and frequently severe mental illness, obsessive-compulsive disorder (OCD) affects millions of people globally. Repetitive behaviours (compulsions) and intrusive thoughts (obsessions) are symptoms of OCD, which may severely limit a person’s capacity to go about their everyday life. Although psychiatric and psychological therapies are the main methods of managing OCD, new developments in neurosurgery, especially Gamma Knife Radiosurgery, give hope to those who are unable to respond to treatment.

Gamma Knife Radiosurgery in Obsessive
Gamma Knife Radiosurgery in Obsessive

This article examines OCD’s characteristics, causes, symptoms, available treatments, and the function of Gamma Knife Radiosurgery in current neuropsychiatric care.

Knowing OCD and the Brain

Neuroimaging research has repeatedly demonstrated that OCD is associated with disruption in the cortico-striato-thalamo-cortical (CSTC) circuit, namely in the orbitofrontal and anterior cingulate cortex. These regions play a role in behaviour control, emotional regulation, and decision-making—all of which are affected in OCD.

Knowing OCD and the Brain
Knowing OCD and the Brain

By making precise lesions or altering activity in specific areas, surgical or radiosurgical intervention aims to control these malfunctioning neuronal circuits in cases that are not responding to treatment.

Obsessive-Compulsive Disorder (OCD): What is it?

OCD is a neuropsychiatric condition characterised by recurrent obsessions and compulsive behaviours.

Obsessive-Compulsive Disorder (OCD)_ What is it
Obsessive-Compulsive Disorder (OCD)_ What is it

Unwanted, intrusive thoughts, desires, or visions that significantly increase worry or distress are referred to as obsessions. Common obsessions include obsessive sexual ideas, a demand for symmetry or exactness, fear of contamination, and fear of hurting oneself or others.

Repetitive actions or thoughts carried out in reaction to obsessions are known as compulsions. Over-washing hands, checking, counting, praying, and putting things in a certain manner are a few examples.

The frequency

About 1% to 2% of people worldwide suffer from OCD, which usually first manifests in late adolescence or early adulthood. Men and women are equally affected.

Reasons and Risks

Although the precise cause and effect of OCD is unknown, it is thought to be caused by an association of:

Reasons and Risks_ Obsessive-Compulsive Disorder (OCD)
Reasons and Risks_ Obsessive-Compulsive Disorder (OCD)
  • Genetic Factors: The risk is increased if OCD runs in the family.
  • Neurobiological Factors: The orbitofrontal cortex, anterior cingulate cortex, and basal ganglia in particular the caudate nucleus are among the brain circuits that are abnormal.
  • Neurochemical Imbalances: One of the main causes is serotonin system dysfunction.
  • Environmental Triggers: Stress, infections, or trauma can all serve as triggers. Examples of these include Paediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal Infections (PANDAS).

Diagnosis

The Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria are used in clinical evaluations to identify OCD. The intensity of symptoms is evaluated using instruments like the Yale-Brown Obsessive Compulsive Scale (Y-BOCS).

Methods of Treatment

  1. CBT, or cognitive behavioural therapy
  • In particular, the most effective psychological treatment is Exposure and Response Prevention (ERP).
  • Aids people in facing their anxieties and avoiding compulsive behaviours.
  1. Drugs
  • Sertraline, fluvoxamine, and fluoxetine are examples of selective serotonin reuptake inhibitors (SSRIs) that are frequently administered.
  • Compared to depression treatment, higher dosages and longer duration of treatment could be required.
  1. DBS, or deep brain stimulation
  • DBS might be taken into consideration for severe, treatment-resistant patients.
  • To modify malfunctioning circuits, electrodes are implanted in particular parts of the brain, such as the anterior limb of the internal capsule or the subthalamic nucleus.
  1. GKR, or Gamma Knife Radiosurgery

Gamma Knife Radiosurgery: What is it?

Gamma Knife Radiosurgery is a non-invasive neurosurgery procedure that targets particular brain regions without making any incisions by using intensely concentrated radiation beams. It doesn’t actually include a knife, despite its name.

 The Process of Gamma Knife Radiosurgery for OCD

One of two brain areas is usually the focus of GKRS for OCD:

  • The internal capsule’s anterior limb (ALIC)
  • Cingulotomy of the cingulate gyrus

The most common radiosurgical procedure for OCD is stereotactic capsulotomy, which involves passing radiation to the ALIC. It is believed that pathological circuits that generate obsessive-compulsive symptoms are disrupted when this area, which connects the thalamus and frontal cortex, is damaged.

Key Steps:

  1. Preoperative Assessment: A multidisciplinary team consisting of a neurosurgeon, neurologist, and psychiatrist evaluates the patient to rule out other diagnoses and confirm treatment-resistant OCD.
  2. Imaging and Planning: MRI and CT images are used to precisely map the brain and plan the radiation dose and trajectory.
  3. Radiosurgery Session: The procedure is often completed in a single session and causes no pain. Since they are conscious, patients can return home that same day.
  4. Follow-up: Symptoms often don’t completely go away for three to twelve months.

Gamma Knife Benefits for OCD

  • Non-invasive: No hospitalisation or incisions
  • Very little chance of bleeding or infection
  • Extremely focused: Little harm to the brain’s surrounding tissue
  • General anaesthesia is not required.
  • Quick recovery from an outpatient procedure

Results and Effectiveness

Research has demonstrated that GKRS can significantly reduce OCD symptoms in patients who are not responding to conventional treatments. Although response rates vary, studies indicate that up to 60–70% of properly chosen patients have clinically significant decreases in the severity of their symptoms as assessed by the Yale-Brown Obsessive-Compulsive Scale (Y-BOCS).

Studies conducted over an extended period of time have likewise shown consistent advantages with few side effects. When adverse effects do happen, they are usually minor and can include headaches, temporary exhaustion, and in rare instances, emotional or cognitive abnormalities.

In conclusion

For those with severe, treatment-resistant OCD, Gamma Knife Radiosurgery is an advanced, evidence-based option. With the promise of better quality of life and functional recovery, it provides a lifeline to those for whom traditional treatments have failed, even if it is not a first-line therapy.

We encourage you to speak with our team of skilled neurosurgical and psychiatric professionals if you or a loved one is experiencing OCD and are thinking about advanced treatment options. They can decide together if Gamma Knife Radiosurgery is the best course of action.

Sources:

  1. https://www.nimh.nih.gov/health/topics/obsessive-compulsive-disorder-ocd
  2. https://iocdf.org/about-ocd/
  3. https://iocdf.org/about-ocd/treatment/gamma-knife/#:~:text=What%20is%20Gamma%20Knife%3F,no%20danger%20to%20brain%20tissue.
  4. https://pmc.ncbi.nlm.nih.gov/articles/PMC8803525/
  5. https://pubmed.ncbi.nlm.nih.gov/35110917/
  6. https://pmc.ncbi.nlm.nih.gov/articles/PMC8803525/

Gamma Knife Radiosurgery in Pineal Region Tumor

Despite its small size, the pineal area of the brain is crucial to neurological function. It can be difficult to diagnose and cure Tumors that develop in this deeply ingrained area. Treatment results have greatly improved with the introduction of sophisticated neurosurgery procedures such as Gamma Knife radiosurgery. A comprehensive explanation of pineal area Tumors, including their symptoms, diagnosis, available treatments, and the function of Gamma Knife therapy, is the goal of this article.

Pineal Region Tumor
Pineal Region Tumor

The Pineal Region: What is it?

The pineal area is situated behind the third ventricle, just above the cerebellum, and between the two cerebral hemispheres, close to the centre of the brain. It contains the pineal gland, a small endocrine gland that produces the hormone melatonin, which controls circadian rhythms, or sleep-wake cycles.

Pineal Region Tumors: What Are They?

Pineal Region Tumors_ What Are They
Pineal Region Tumors_ What Are They

Less than 1% of all brain Tumors are pineal area Tumors, making them extremely uncommon. The pineal gland itself or nearby tissues including brain tissue, meninges, or germ cells may give rise to these Tumors.

Typical Pineal Region Tumor Types:

Typical Pineal Region Tumor Types
Typical Pineal Region Tumor Types
  • The most prevalent malignant Tumor in this region is a germinoma.
  • Benign and slowly developing pineocytomas
  • Pineoblastomas (aggressive, high grade)
  • Teratomas
  • Gliomas
  • Meningiomas
  • Mixed germ cell Tumors and atypical Tumors

Why Do Pineal Tumors Occur?

The majority of pineal Tumors occur irregularly, which means their source is unknown.

Nevertheless, genetic changes that lead to abnormal or confused cells growing out of control can result in pineal Tumors. They may also result from abnormalities in the development of the embryo. Germ cells, for instance, usually move to develop into reproductive organs. However, some of these cells may subsequently grow into Tumors if they stay in the brain.

Even though they are uncommon, some pineal Tumors are linked to genetic disorders such as Li-Fraumeni Syndrome, which is brought on by TP53 gene abnormalities, or retinoblastoma, a rare and rapidly spreading hereditary eye cancer. Your risk of developing brain Tumors may be elevated by either of these hereditary diseases.

Pineal Region Tumor Symptoms

Pineal Region Tumor Symptoms
Pineal Region Tumor Symptoms

Because of the pineal gland’s deep location and close closeness to important brain areas, even small Tumors can produce serious symptoms like:

  • Headache (caused by hydrocephalus or elevated intracranial pressure)
  • Vomiting and feeling nauseous
  • Parinaud’s syndrome, a defining feature of pineal Tumors, is the inability to move the eyes upward.
  • Double or blurred vision
  • Unbalanced or poorly coordinated
  • Less common seizures
  • Endocrine disorders (caused by melatonin or hormone pathway imbalance)

Diagnostics of Pineal Tumors

Neurological examinations, imaging studies, and laboratory work are frequently used in the diagnosis of pineal Tumors.

When diagnosing a pineal Tumor, the following instruments are frequently employed:

  1. Physical and neurological examination: Your doctor will first enquire about your general health, symptoms, and any potential risk factors. They will then conduct an examination to evaluate your neurological function, including reflexes, strength, coordination, sensation, and eye movements. This is because some problems with eye motions may indicate abnormalities in the pineal region.
  2. Ophthalmologic examination: An eye specialist may be called upon to assess your visual acuity and search for indications of elevated intracranial pressure, as pineal Tumors are known to cause symptoms connected to vision.
  3. The main imaging technique for detecting and diagnosing pineal Tumors is magnetic resonance imaging (MRI), which produces fine-grained images of the brain that can be used to determine the location, size, and features of a Tumor. To distinguish the Tumor from the surrounding tissues and assess its spread, an MRI with contrast may be utilised.
  4. Computed Tomography (CT): A CT scan uses X-rays to produce fine-grained cross-sectional brain images that aid in determining the size and location of a Tumor, even though an MRI is frequently the first option in neuroimaging. Additionally, calcifications, which are typical of pineal Tumors, and hydrocephalus can be detected using CT scans.
  5. A spinal tap, sometimes referred to as a lumbar puncture, is a procedure in which a needle is placed into the lower back to draw cerebrospinal fluid (CSF) in order to check for the presence of malignant cells. If your Tumor has spread throughout the central nervous system (CNS), this test can identify it.
  6. Blood tests: Certain pineal Tumors, especially germ cell Tumors, emit high levels of beta-human chorionic gonadotropin (hCG) or alpha-fetoprotein (AFP) in the blood or cerebrospinal fluid (CSF), which aids in the diagnosis of certain pineal Tumors.
  7. Biopsy: A biopsy is required if your imaging results point to a Tumor. A tiny sample is taken from the Tumor during a biopsy and sent to a pathology lab for examination. In order to identify the sort of cells present and other crucial features that inform treatment choices, pathologists there look at the tissue under a microscope. A biopsy is usually performed surgically or via stereotactic biopsy for brain Tumors.

Depending on the nature and degree of your pineal Tumor, more testing might be required.

Options for Treatment

The tumor’s nature, size, location, and grade, as well as the patient’s general condition, all influence the treatment plans.

  1. Observation

If small, benign Tumors like pineocytomas are not causing symptoms, they can be tracked with routine imaging.

  1. Resection via Surgery
  • Recommended for huge, symptomatic, or accessible Tumors.
  • Techniques include endoscopic, transcallosal, and infratentorial supracerebellar techniques.
  • Hydrocephalus can also be relieved surgically (e.g., by conducting an endoscopic third ventriculostomy or installing a ventriculoperitoneal shunt).
  1. Treatment with Radiation
  • Used frequently for malignant Tumors such as pineoblastomas or germinomas after surgery.
  • Can be applied as the main course of treatment for some Tumors that are susceptible to radiation.
  1. The use of chemotherapy
  • Very useful for germ cell Tumors.
  • Frequently used in combination with radiation therapy for a better outcome.

Gamma Knife in Tumors of the Pineal Region

A non-invasive therapeutic method called Gamma Knife radiosurgery uses concentrated gamma radiation beams to target brain Tumors with sub-millimeter precision. It works particularly well for Tumors that are deep, difficult to access, or still present in the pineal region.

Gamma Knife Radiosurgery Advantages:

Gamma Knife Stereotactic Radiosurgery
Gamma Knife Stereotactic Radiosurgery
  • Minimally invasive: doesn’t require general anaesthesia or incisions.
  • Targeted precisely: Preserves the area around healthy brain tissue.
  • Quick recovery: Frequently carried out as an outpatient operation.
  • Perfect for little or persistent Tumors following surgical excision.
  • Low incidences of complications.

Gamma Knife Indications for Pineal Tumors:

  • Tumors that are inoperable or inaccessible during surgery.
  • Unsuitable patients for open surgery.
  • Recurring Tumors following the first radiation or surgery.
  • Tumor tissue that remains after partial resection.
  • Adjunct therapy for low-grade gliomas, meningiomas, and pineocytomas.

Restrictions:

  • Not appropriate for big Tumors that cause hydrocephalus or a substantial bulk effect.
  • Delayed Tumor shrinkage—it could take weeks or months to see results.

The outlook

Depending on the form and grade of the Tumor, the prognosis for pineal area Tumors varies greatly:

  • With combination chemotherapy and radiation, germinomas have a very good prognosis (cure rates of over 90%).
  • When removed surgically, pineocytomas have a favourable prognosis.
  • Despite multimodal treatment, high-grade gliomas and pineoblastomas have a guarded prognosis and are more aggressive.
  • Results are greatly enhanced by early diagnosis and individualised therapy, including radiosurgery.

In Conclusion

Despite being uncommon, pineal area Tumors necessitate a comprehensive approach from radiation specialists, neurosurgeons, neuro-oncologists, and radiologists. Patients now have access to precise, efficient, and minimally invasive choices thanks to advancements like Gamma Knife radiosurgery, which improves survival and quality of life.

Better results may result from early evaluation by a specialised neurosurgery team if you or a loved one has been diagnosed with a pineal area Tumor. To deliver individualised, evidence-based care, AIIMS Delhi is equipped with cutting-edge diagnostic and therapeutic instruments, such as Gamma Knife technology.                                                                                                                                                                

Sources:

  1. https://pmc.ncbi.nlm.nih.gov/articles/PMC8036741/
  2. https://www.cancer.gov/rare-brain-spine-tumor/tumors/pineal-region-tumors
  3. https://www.ncbi.nlm.nih.gov/books/NBK560567/
  4. https://www.barrowneuro.org/condition/pineal-tumors/
  5. https://www.webmd.com/brain/what-to-know-about-pineal-tumors
  6. https://emedicine.medscape.com/article/249945-overview?form=fpf
  7. https://www.cancerresearchuk.org/about-cancer/brain-Tumors/types/pineal-region-Tumors
  8. https://radiopaedia.org/articles/pineal-region-mass
  9. https://pmc.ncbi.nlm.nih.gov/articles/PMC4617952/
  10. https://pubmed.ncbi.nlm.nih.gov/18081477/
  11. https://www.jkns.or.kr/journal/view.php?number=1820
  12. https://www.jkns.or.kr/upload/pdf/0042006160.pdf

Gamma Knife Radiosurgery in Intracranial Angiosarcoma

An extremely uncommon and violent malignant tumour that develops from the endothelial cells lining the brain’s blood arteries is called an intracranial angiosarcoma. It presents considerable difficulties in diagnosis, therapy, and long-term management because of its rarity and highly vascular character. Even though this condition is rare, it must be understood in order to improve patient outcomes and act immediately.

Intracranial Angiosarcoma
Intracranial Angiosarcoma

What is it? (Intracranial Angiosarcoma)

One kind of soft tissue sarcoma that develops from vascular or lymphatic endothelial cells is called angiosarcoma. The term “intracerebral angiosarcoma” describes the tumor’s appearance inside the cranial cavity, while the majority of angiosarcomas develop in the skin, soft tissue, liver, heart, or breast. It could affect the dura mater, intracranial vascular, or brain parenchyma.

Important Features:

Important Features_ Intracranial Angiosarcoma
Important Features_ Intracranial Angiosarcoma
  • Extremely hostile and prone to quick growth.
  • High risk of bleeding due to a rich vascular supply.
  • Either primary (originating in the cranium) or secondary (originating elsewhere).
  • Primarily impacts middle-aged individuals, while incidences have also been documented in older and paediatric populations.
  • Has radiologic similarities to other vascular tumours or hemorrhagic lesions, making diagnosis difficult.

Clinical Presentations

Clinical Presentations_ Intracranial Angiosarcoma
Clinical Presentations_ Intracranial Angiosarcoma

The size, location, and development rate of the tumour all affect the symptoms of cerebral angiosarcoma, which are frequently non-specific. Typical signs and symptoms include:

  • Chronic headaches
  • Seizures
  • Deficits in the nervous system (e.g., weakness, sensory abnormalities)
  • Papilledema and vomiting are symptoms of elevated intracranial pressure.
  • Changes in mental state
  • Abrupt neurological deterioration brought on by tumour bleeding

Its aggressive nature causes these symptoms to deteriorate quickly over time.

Diagnosis

Diagnosis_ Intracranial Angiosarcoma
Diagnosis_ Intracranial Angiosarcoma
  1. Imaging:

The main modality is MRI with contrast, which usually shows a heterogeneous, enhancing mass with necrotic and bleeding regions. Nevertheless, the imaging results are not definitive and frequently resemble other intracranial tumours including glioblastomas, hemangioblastomas, or metastases.

  • The study of histopathology

Histopathological analysis after biopsy or surgical removal is necessary for a conclusive diagnosis. Important conclusions include:

  • Uneven vascular channels formed by malignant endothelial cells
  • Elevated mitotic activity
  • Positive immunohistochemistry results for FLI-1, ERG, CD31, and CD34

Strategies for Treatment

The treatment of cerebral angiosarcoma is multimodal and patient-specific due to its aggressive nature.

  1. Resection via Surgery

When possible, surgical excision continues to be the primary form of care. Because of the vascularity of the tumour, intraoperative bleeding frequently complicates surgery. Complete excision might not always be feasible, particularly in deep-seated or eloquent brain regions.

  1. Radiation therapy

To lower the chance of a local recurrence, post-operative radiation is frequently used. Depending on the size and location of the tumour, either stereotactic radiosurgery or conventional fractionated radiation may be utilised.

  1. The use of chemotherapy

Based on procedures for soft tissue sarcomas, chemotherapy medicines such paclitaxel, doxorubicin, or ifosfamide have been utilised, although the exact role of chemotherapy is still unknown due to a lack of data. Immunotherapy and targeted therapeutics are being investigated.

Intracranial Angiosarcoma and Gamma Knife Radiosurgery

A type of stereotactic radiosurgery called Gamma Knife Radiosurgery (GKRS) spares the surrounding healthy brain tissue while precisely delivering high-dose radiation beams to intracranial lesions. It works especially well for vascular tumours and tumours in difficult-to-operate places.

Function in Angiosarcoma Intracranial:

Although it is not a first-line treatment, Gamma Knife radiosurgery is crucial in adjuvant or palliative settings. It is useful for:

  • For recurring or persistent tumour tissue after surgery.
  • Is the main treatment for patients who are not suitable for surgery.
  • In the treatment of brain-metastasized angiosarcomas.
  • To reduce the risk of bleeding in highly vascularised tumors.

Gamma Knife benefits include:

Gamma Knife benefits include_ Intracranial Angiosarcoma
Gamma Knife benefits include_ Intracranial Angiosarcoma
  • Outpatient, non-invasive procedure
  • Accurate targeting reduces harm to nearby structures.
  • Less chance of bleeding than with open surgery
  • In certain cases, local tumour management is effective.

Restrictions:

  • Appropriate for tumours with a considerable volume
  • Systemic therapy may still be necessary.
  • Due to its rarity, long-term results in cases unique to angiosarcoma are not well reported.

The outlook

For patients with intracranial angiosarcoma, the prognosis is still uncertain. Because of the tumor’s aggressive nature and high recurrence rates, survival prospects are typically poor. Although early detection, total surgical resection, and adjuvant therapy like Gamma Knife Radiosurgery may improve results in some individuals, the median survival is frequently less than a year.

In conclusion

An uncommon but dangerous brain tumour, intracranial angiosarcoma is known for its high recurrence rate, rapid growth, and risk of bleeding. For the best care, an integrated group of neurosurgeons, oncologists, radiation therapists, and pathologists is essential. A useful tool in the neurosurgical toolbox, innovations like Gamma Knife Radiosurgery provide targeted therapy with fewer problems, particularly for tumours in surgically difficult sites.

To choose the best and most individualised course of therapy if you or a loved one has been diagnosed with intracranial angiosarcoma, it is essential to speak with a skilled neurosurgery team. 

Source:

  1. https://pmc.ncbi.nlm.nih.gov/articles/PMC6895451/#sec7
  2. https://www.cancer.gov/pediatric-adult-rare-tumor/rare-tumors/rare-vascular-tumors/angiosarcoma#:~:text=You%20may%20have%20pain%20in,possible%20to%20feel%20the%20lump.
  3. https://www.pennmedicine.org/cancer/types-of-cancer/sarcoma/types-of-sarcoma/soft-tissue-sarcoma/angiosarcoma
  4. https://pubmed.ncbi.nlm.nih.gov/19467792/
  5. https://www.researchgate.net/publication/389465636_Gamma_Knife_Radiosurgery_in_Intracranial_Angiosarcoma
  6. https://www.sciencedirect.com/science/article/abs/pii/S0360301609002235
  7. https://diagnosticpathology.biomedcentral.com/articles/10.1186/s13000-023-01389-7
  8. https://my.clevelandclinic.org/health/diseases/22778-angiosarcoma
  9. https://www.researchgate.net/figure/A-proposed-flow-chart-for-the-treatment-of-intra-cranial-angiosarcoma_fig6_230713175

Gamma Knife Surgery in Intracranial Dural Arteriovenous Fistulas

Rare but potentially dangerous brain vascular anomalies are called intracranial dural arteriovenous fistulas (dAVFs). They have to do with abnormal artery-vein connections in the dura mater, the brain’s outermost layer. In contrast to congenital arteriovenous malformations (AVMs), dAVFs are usually acquired lesions that may arise later in life as a result of venous thrombosis, trauma, infection, or surgery. Certain dAVFs might result in life-threatening bleeding or severe neurological impairments if treatment is not received.

A Dural Arteriovenous Fistula: What Is It?

A Dural Arteriovenous Fistula_ What Is It
A Dural Arteriovenous Fistula_ What Is It

An irregular direct connection between the meningeal arteries and the dural venous sinuses or cortical veins is known as a dural arteriovenous fistula (dAVF). Blood normally travels from arteries to capillaries and finally to veins. This capillary bed is bypassed in a dAVF, allowing high-pressure arterial blood to enter the low-pressure venous system directly. Depending on the drainage pattern and location, this can cause neurological symptoms, venous congestion, or haemorrhage.

Reasons/Causes and Dangers

Reasons_Causes and Dangers
Reasons_Causes and Dangers

A number of factors are linked to the development of dAVFs, though their exact cause is not always evident:

  • Thrombosis of the dural sinuses
  • Head injuries
  • Neurosurgical techniques
  • Infections
  • States of hypercoagulability

With no obvious gender preference, they are most frequently observed in middle-aged to older persons.

The symptoms of the Intracranial Dural Arterivenous Fistula are as follows:

The size, location, and blood flow pattern of dAVFs all affect the symptoms. While some may show up with serious neurological problems, others may stay asymptomatic and be found by chance.

Typical signs and symptoms include:

Typical signs and symptoms include
Typical signs and symptoms include
  • A headache
  • Hearing a rhythmic sound in the ear is known as pulsatile tinnitus.
  • Visual disruptions
  • Seizures
  • Deficits in the cranial nerve
  • Dementia-like symptoms or cognitive decline
  • Haemorrhage inside the brain (in high-grade fistulas)

Classification

Based on their venous drainage patterns and haemorrhage risk, dAVFs are categorised using the Cognard and Borden categorisation systems.

Classification by Borden:

  • Type I: Low risk drainage into a venous sinus
  • Type II: Retrograde cortical venous drainage into a venous sinus (moderate risk)
  • Type III: High-risk direct cortical venous drainage

Classification by Cognard:

Varies according to venous drainage patterns and flow direction, ranging from Type I (benign) to Type V (most aggressive).

Diagnosis

In order to avoid complications, early diagnosis is essential. The imaging modalities that are employed include:

  • For preliminary evaluation, magnetic resonance imaging (MRI) and magnetic resonance angiography (MRA) are helpful.
  • Computed Tomography Angiography (CTA): May reveal abnormal veins and swollen feeding arteries.
  • The gold standard for diagnosis is digital subtraction angiography (DSA), which offers fine-grained visualisation of the venous drainage, feeding arteries, and fistula.

Options for Treatment

Options for Treatment
Options for Treatment

The dAVF’s categorisation, location, and symptoms all influence the therapy option. The goal of treatment is to restore normal venous drainage and close the abnormal link.

  1. Embolisation of Endovascular

  • A minimally invasive procedure in which the fistula is sealed shut by administering embolic chemicals via a catheter.
  • Frequently the initial course of treatment.
  1. Resection by Microsurgery

  • Used when embolisation is impractical or fails.
  • Involves cutting the fistula directly during surgery.
  1. Gamma Knife Surgery, or stereotactic radiosurgery

Gamma Knife Stereotactic Radiosurgery
Gamma Knife Stereotactic Radiosurgery
  • An approach for non-invasive therapy that works especially well for residual or low-flow fistulas.

Intracranial Dural Arteriovenous Fistulas with Gamma Knife Surgery

A type of stereotactic radiosurgery known as “gamma knife” (GKS) uses concentrated, high-dose radiation beams to precisely target the abnormal vascular connections inside the dura while preserving the surrounding healthy brain tissue.

How It Operates:

  • Through damage to endothelial cells and vessel wall thickening, the radiation causes the unusual vessels to gradually close over the course of months to years.
  • It is usually applied to individuals who are not a good candidate for invasive procedures or to low-grade or persistent dAVFs following unsuccessful embolisation.

Gamma Knife Surgery Indications for dAVFs:

  • Tiny, persistent fistulas following embolisation
  • Deeply seated or inaccessible surgical sites
  • Low-risk dAVFs that are asymptomatic or only slightly symptomatic
  • Comorbidities in patients that raise the risk of surgery

Benefits:

  • Non-invasive
  • Procedure for outpatients
  • Short recovery period
  • Suitable for use in conjunction with additional therapies

Limitations:

  • Effect delayed: Total obliteration may take six to thirty-six months.
  • Not appropriate for high-grade or quickly developing fistulas with cortical venous reflux.
  • The evaluation of obliteration requires routine follow-up imaging.

Prognosis and Follow-Up

The fistula’s classification and drainage pattern determine the prognosis. While low-risk dAVFs can be seen, high-risk ones need to be treated right away.

Follow-up consists of:

  • DSA or serial MRI/MRA
  • Preventing recurrence
  • Neurological evaluation

In most situations, a favourable outcome can be achieved with appropriate diagnosis and treatment. For certain cases, Gamma Knife Surgery has demonstrated exceptional obliteration rates with little adverse consequences.

In conclusion

Vascular abnormalities known as intracranial dural arteriovenous fistulas are complicated but curable. For the best results, a multidisciplinary strategy including radiation oncologists, neurosurgeons, and interventional neuroradiologists is essential. For some forms of dAVFs, Gamma Knife Surgery has become a potent non-invasive treatment option, particularly when embolisation or traditional surgery may be unsafe or insufficient.

Early contact with a specialised neurosurgery team can significantly impact treatment outcomes and quality of life if you or a loved one is diagnosed with a dAVF.

Sources:

  1. https://pmc.ncbi.nlm.nih.gov/articles/PMC8013238/#sec10
  2. https://pmc.ncbi.nlm.nih.gov/articles/PMC5435465/
  3. https://radiopaedia.org/articles/dural-arteriovenous-fistula
  4. https://www.ahajournals.org/doi/10.1161/strokeaha.115.008228
  5. https://my.clevelandclinic.org/health/diseases/dural-arteriovenous-fistula-davf
  6. https://www.mayoclinic.org/diseases-conditions/dural-arteriovenous-fistulas/symptoms-causes/syc-20364280
  7. https://link.springer.com/article/10.1007/s13760-022-02133-6

Gamma-Knife Stereotactic Radiosurgery for Large Vestibular

The Schwann cells that surround the vestibular nerve, which controls hearing and balance, give birth to benign tumours called vestibular schwannomas, sometimes referred to as acoustic neuromas. Symptoms including hearing loss, imbalance, facial numbness, and in extreme situations, brainstem compression, can result from these tumours’ gradual growth and eventual pressure against nearby brain structures.

Gamma-Knife Stereotactic Radiosurgery for Large Vestibular
Gamma-Knife Stereotactic Radiosurgery for Large Vestibular

Microsurgical excision has historically been used to treat big vestibular schwannomas. However, even for big vestibular schwannomas in properly chosen individuals, Gamma Knife Stereotactic Radiosurgery (GKRS) has become a less invasive and successful therapeutic option due to technological developments and a better understanding of tumour biology.

Gamma Knife Stereotactic Radiosurgery: What is it?

Gamma Knife Stereotactic Radiosurgery
Gamma Knife Stereotactic Radiosurgery

With little effect on nearby healthy tissue, Gamma Knife Radiosurgery is a non-invasive, image-guided treatment technique that targets a particular area of the brain with a highly concentrated radiation dose. No “knife” or incision is used, despite the name.

It delivers a potent dose exactly to the tumour by utilising hundreds of coordinated gamma radiation beams that converge on a single location. The tumor’s DNA gets damaged as a result, which slows its growth and eventually causes it to shrink.

How Does It Operate?

Stereotactic guiding, which makes use of 3D imaging (MRI and CT scans) and a stereotactic frame or mask to guarantee the tumour is precisely targeted, is the secret to the Gamma Knife’s accuracy.

Important Steps in the Process:

  • Imaging & Planning: A 3D model of the tumour can be produced with the use of MRI/CT scans.
  • Treatment Planning: Using cutting-edge tools, neurosurgeons and radiation oncologists create a personalised treatment plan.
  • Positioning: To guarantee that the patient stays motionless, a stereotactic head frame or frameless mask is utilised.
  • Radiation Delivery: Depending on the size and dosage of the tumour, the patient rests in the Gamma Knife machine for 30 to 2 hours.
  • After the procedure, patients usually leave the hospital the same day and return home.

Gamma Knife Treatment for Large Vestibular Schwannomas

Gamma Knife Treatment for Large Vestibular Schwannomas
Gamma Knife Treatment for Large Vestibular Schwannomas

For small to medium-sized vestibular schwannomas, Gamma Knife Radiosurgery has long been used as a primary or adjuvant treatment. However, the strategy needs to be carefully considered when dealing with larger tumours (usually >2.5-3 cm in diameter).

Problems with Big Tumours:

  • Risk of brainstem compression
  • Increased risk of swelling (oedema) after treatment
  • Increased mass effect resulting in neurological manifestations

A Modern Method for Huge Tumours:

  1. Fractionated or staged radiosurgery: To reduce side effects and give the brain time to adjust, radiation may be administered across several sessions rather than all at once.
  2. Resection of the Subtotal Subsequent to GKRS: A frequently used approach involves removing a piece of the tumour physically in order to decompress the brainstem, and then controlling the remaining tumour using radiosurgery.
  3. Selecting Patients Carefully: GKRS is not appropriate for all big vestibular schwannomas. Important factors to take into account include the patient’s age, symptoms, tumour size, location, and general health.

Gamma Knife Advantages for Big Vestibular Schwannomas

Gamma Knife Advantages for Big Vestibular Schwannomas
Gamma Knife Advantages for Big Vestibular Schwannomas
  • Non-invasive: doesn’t require general anaesthesia, scalpels, or incisions.
  • Preservation of Nerve Function: Compared to open surgery, there is a greater chance of protecting the hearing and facial nerves.
  • Short Recovery Time: Within one to two days, the majority of patients return to their regular activities.
  • Low Risk of Bleeding or Infection
  • Procedure for Outpatients

Risks and Adverse Effects

Even while Gamma Knife is thought to be safe, especially when handled by skilled individuals, possible adverse effects could include:

  • Immediately following the surgery, a headache or nausea
  • Momentary weakness or numbness in the face
  • Peritumoral oedema, or swelling surrounding the tumour, can cause symptoms like feeling dizzy or trouble balancing.
  • Delayed hearing loss, especially when there is a pre-existing hearing impairment
  • Frequent MRI follow-up is necessary to track tumour response and identify any postponed problems.

Results and Effectiveness

Several studies have demonstrated that, even in certain situations of massive vestibular schwannomas, Gamma Knife achieves tumour control rates of 90–95%. Most tumours stabilise or decline over months to years, however quick reduction is rare. Functional results are better than surgery, particularly when it comes to the preservation of facial nerves.

Radiosurgery provides the best compromise between minimising bulk effect and preserving neurological function when paired with subtotal resection. 

In conclusion

A new approach in the treatment of vestibular schwannomas is represented by Gamma Knife Stereotactic Radiosurgery. This non-invasive, precision-guided treatment can provide excellent tumour control with few side effects for large vestibular schwannomas, particularly in older patients or those with comorbidities.

To identify the best course of treatment, a multidisciplinary examination involving neurosurgeons and radiosurgery specialists is essential if you or a loved one has been diagnosed with vestibular schwannoma, especially a large one.

Sources:

  1. https://www.nidcd.nih.gov/health/vestibular-schwannoma-acoustic-neuroma-and-neurofibromatosis
  2. https://en.wikipedia.org/wiki/Vestibular_schwannoma
  3. https://www.ncbi.nlm.nih.gov/books/NBK562312/\
  4. https://pmc.ncbi.nlm.nih.gov/articles/PMC9272253/#JR200335-1
  5. https://pubmed.ncbi.nlm.nih.gov/28707997/
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  8. https://www.jkns.or.kr/upload/pdf/0042007122.pdf
  9. https://www.cambridge.org/core/journals/canadian-journal-of-neurological-sciences/article/gamma-knife-radiosurgery-for-large-vestibular-schwannomas-a-canadian-experience/C42BF9C4E1D62BD6A4282EA120CA7899
  10. https://radiopaedia.org/articles/vestibular-schwannoma

Gamma Knife Radiosurgery for Spetzler-Martin Grade III Cerebral Arterio-Venous Malformations

Abnormal blood artery tangles that join arteries and veins in the brain are known as cerebral arteriovenous malformations (AVMs), and they can interfere with regular blood flow and oxygen circulation. The Spetzler-Martin grading system is still the most commonly used classification scheme for evaluating AVMs. It uses venous drainage patterns, size, and placement in relation to sensitive brain areas to categorise AVMs.

Gamma Knife Radiosurgery for Spetzler-Martin Grade III Cerebral Arterio-Venous Malformations
Gamma Knife Radiosurgery for Spetzler-Martin Grade III Cerebral Arterio-Venous Malformations

Martin Spetzler Because of its intermediate complexity, grade III AVMs are a particularly difficult category that frequently necessitates a multimodal, advanced approach to therapy. Gamma Knife Radiosurgery (GKRS) is a refined, minimally invasive procedure that is accessible for a limited number of patients. This article examines the mechanics, patient selection, results, and long-term advantages of using a Gamma Knife to treat Grade III AVMs.

Gamma Knife Radiosurgery: What Is It?

Knife Gamma Radiosurgery is a type of stereotactic radiosurgery (SRS) that targets brain abnormalities precisely without requiring a surgical incision by using highly concentrated gamma radiation beams. Despite its name, this non-invasive outpatient technique is not a knife and does not require any cutting.

Over 190 individual gamma radiation beams are delivered by the Gamma Knife devices, which converges on a precise location to give the AVM a significant dose while preserving the nearby healthy brain tissue. The AVM vessels thicken and shut down as a result of the radiation over time, eventually removing the abnormality.

Why Spetzler-Martin Grade III AVMs Are Different ?

Why Spetzler-Martin Grade III AVMs Are Different
Why Spetzler-Martin Grade III AVMs Are Different

The following defines Spetzler-Martin Grade III AVMs:

  • Size: Medium (3–6 cm across)
  • Eloquent location: Could be found in important regions such as language centres, vision circuits, or the sensorimotor cortex.
  • Deep venous drainage may be a part of venous drainage.

These AVMs fall somewhere in between being too big or complicated to categorically necessitate open surgery and too small for simple radiosurgical obliteration. Because of its intermediate nature, treatment choices need to be tailored to each patient.    

 Gamma Knife Indications for Grade III AVMs

Gamma Knife Indications for Grade III AVMs
Gamma Knife Indications for Grade III AVMs

Particularly helpful applications for Gamma Knife Radiosurgery include the following:

  • AVMs in expressive brain regions where there is a high risk of morbidity after surgical resection
  • AVMs with profound venous drainage or deep-seated lesions
  • Patients with medical comorbidities that make them unsuitable candidates for surgery
  • After surgical excision, residual AVM
  • The patient prefers a non-invasive therapy approach.

It is frequently employed together with surgery or embolisation as part of a multimodal approach.

Overview of the Procedure

1. Pre-Procedure Assessment:

  • A thorough medical history and examination
  • To define AVM anatomy, MRI/MRA, CT Angiography, and Digital Subtraction Angiography (DSA) are used.
  • Verification of Spetzler-Martin grading

2. Positioning of the Head Frame or Mask:

  • For localisation, a frameless mask or stereotactic head frame is utilised (for maximum accuracy).

3. Planning and Imaging:

  • Imaging at high resolution is used to see the AVM nidus.
  • Medical physicists, neurosurgeons, and radiation oncologists work together to create a treatment strategy. 

4. Delivery of Radiosurgery:

Delivery of Radiosurgery
Delivery of Radiosurgery
  • The Gamma Knife unit is positioned within the patient.
  • Depending on the size of the nidus, radiation is administered painlessly for 30 to 2 hours.

5. After the procedure:

  • Usually, patients are released on the same day.
  • Normal activities can frequently be resumed soon, and there is no need for a hospital stay or recovery period.

Results and Effectiveness

  • Obliteration Rates: Within two to four years after treatment, total obliteration rates for Grade III AVMs vary from 50% to 80%.
  • Risk of Haemorrhage: Patients are still susceptible to bleeding during the latency period, which is before the AVM is completely destroyed. The risk of bleeding occurs between 2% and 4% every year.
  • Neurological Preservation: Gamma Knife is a safer option than surgery since high rates of neurological preservation have been documented when the AVM is situated in eloquent regions.
  • Long-Term Monitoring: To verify obliteration and keep an eye out for recurrence, routine follow-up with MRI and DSA is crucial.

Gamma Knife Benefits for Grade III AVMs

  • No incision and minimally invasive
  • Decreased chance of neurological impairments, particularly in expressive areas
  • Outpatient treatment with little recovery time
  • Repetitible or able to be mixed with different modalities
  • Damage to healthy brain tissue is reduced by highly precise targeting.

Restrictions & Things to Think About

  • Delayed Effect: It may take years for removal to occur.
  • Not Fit for Every AVM: Diffuse or very big AVMs could not react well.
  • Residual Haemorrhage Risk: There is a chance of rupture until obliteration is accomplished.
  • Headache, edema, and infrequently, radiation necrosis are examples of radiation side effects.

In conclusion

For the treatment of Spetzler-Martin Grade III cerebral AVMs, especially those found in deep or eloquent brain regions, Gamma Knife Radiosurgery provides a non-invasive, safe, and efficient alternative. Even though it might not offer a quick fix, its great accuracy and little rate of complications make it an invaluable tool in the neurosurgical toolbox.

The optimal course of treatment, which may include a combination of surgery, embolisation, and radiosurgery depending on the patient’s AVM architecture and general health, requires multidisciplinary review.

Offering life-altering outcomes without the hazards associated with standard surgery, Gamma Knife Radiosurgery is a ray of hope for patients and their families seeking therapy options for difficult AVMs.

Sources:

  1. https://pubmed.ncbi.nlm.nih.gov/12657169/
  2. https://pmc.ncbi.nlm.nih.gov/articles/PMC8324218/
  3. https://radiopaedia.org/articles/spetzler-martin-arteriovenous-malformation-grading-system-2
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