Oligodendroglioma (patient information)
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Editor-in-Chief: C. Michael Gibson, M.S.,M.D. [1] Phone:617-632-7753; Associate Editor-In-Chief: Sara Mohsin, M.D.[2] Jinhui Wu, MD
Overview
Oligodendroglioma is a type of glioma. It occupies about 4% of brain tumors. This type of brain tumor origins from the oligodendrocytes which make myelin, a substance that surrounds and insulates axons of the brain and spinal cord. Oligodendroglioma occurs primarily in adults and only rarely found in children. Usual symptoms include headache, hydrocephalus, nausea and vomiting, seizure, weakness, or numbness in the extremities. Sometimes oligodendroglioma may spread along the cerebrospinal fluid pathways but rarely spread outside the brain or spinal cord. Treatments include surgery, radiation therapy, chemotherapy, gene therapy, or a combination of them. Because oligodendroglioma may infiltrate nearby brain tissue, it cannot be completely removed by surgery. Prognosis of oligodendroglioma depends on the grade of the cancer.
Brain tumor - primary - adults
A primary brain tumor is a group (mass) of abnormal cells that start in the brain.
Causes
Primary brain tumors include any tumor that starts in the brain. Primary brain tumors can start from brain cells, the membranes around the brain (meninges), nerves, or glands.
Tumors can directly destroy brain cells. They can also damage cells by producing inflammation, placing pressure on other parts of the brain, and increasing pressure within the skull.
The cause of primary brain tumors is unknown. There are many risk factors that could play a role:
Radiation therapy used to treat brain cancers increases the risk of brain tumors up to 20 or 30 years later. Some inherited conditions increase the risk of brain tumors, including neurofibromatosis, Von Hippel-Lindau syndrome, Li-Fraumeni syndrome, and Turcot syndrome. Lymphomas that begin in the brain in people with a weakened immune system are sometimes linked to infection by the Epstein-Barr virus. These have not proven to be risk factors:
Exposure to radiation at work, or to power lines, cell phones, cordless phones, or wireless devices Head injuries Smoking Hormone therapy SPECIFIC TUMOR TYPES
Brain tumors are classified depending on:
Location of the tumor Type of tissue involved Whether they are noncancerous (benign) or cancerous (malignant) Other factors Sometimes, tumors that start out less aggressive can change their biologic behavior and become more aggressive.
Tumors can occur at any age, but many types are most common in a certain age group. In adults, gliomas and meningiomas are the most common.
Gliomas come from glial cells such as astrocytes, oligodendrocytes, and ependymal cells. Gliomas are divided into three types:
Astrocytic tumors include astrocytomas (can be noncancerous), anaplastic astrocytomas, and glioblastomas. Oligodendroglial tumors. Some primary brain tumors are made up of both astrocytic and oligodendrocytic tumors. These are called mixed gliomas. Glioblastomas are the most aggressive type of primary brain tumor. Meningiomas and schwannomas are two other types of brain tumors. These tumors:
Occur most often between ages 40 and 70. Are usually noncancerous, but can still cause serious complications and death from their size or location. Some are cancerous and aggressive. Other primary brain tumors in adults are rare. These include:
Ependymomas Craniopharyngiomas Pituitary tumors Primary (central nervous system - CNS) lymphoma Pineal gland tumors Primary germ cell tumors of the brain
Types of Brain and Spinal Cord Tumors in Adults
Tumors that start in the brain (primary brain tumors) are not the same as tumors that start in other organs, such as the lung or breast, and then spread to the brain (metastatic or secondary brain tumors). In adults, metastatic tumors to the brain are actually more common than primary brain tumors. These tumors are not treated the same way. For example, breast or lung cancers that spread to the brain are treated differently from tumors that start in the brain.
Unlike cancers that start in other parts of the body, tumors that start in the brain or spinal cord rarely spread to distant organs. Even so, brain or spinal cord tumors are rarely considered benign (non-cancerous). They can still cause damage by growing and spreading into nearby areas, where they can destroy normal brain tissue. And unless they are completely removed or destroyed, most brain or spinal cord tumors will continue to grow and eventually be life-threatening.
Primary brain tumors can start in almost any type of tissue or cell in the brain or spinal cord. Some tumors have mixed cell types. Tumors in different areas of the central nervous system (CNS) may be treated differently and have a different prognosis (outlook).
Brain and spinal cord tumor grades Some brain and spinal cord tumors are more likely to grow into nearby tissues (and to grow quickly) than are other tumors. The World Health Organization (WHO) divides brain and spinal cord tumors into 4 grades (using Roman numerals I to IV), based largely on how the cells look under the microscope:
Grade I: These tumors typically grow slowly and do not grow into (invade or infiltrate) nearby tissues. They can often be cured with surgery. Grade II: These tumors also tend to grow slowly but they can grow into nearby brain tissue. They are more likely to come back after surgery than grade I tumors. They are also more likely to become faster-growing tumors over time. Grade III: These tumors look more abnormal under the microscope. They can grow into nearby brain tissue and are more likely to need other treatments in addition to surgery. Grade IV: These are the fastest growing tumors. They generally require the most aggressive treatment. Gliomas Gliomas are not a specific type of brain tumor. Glioma is a general term for tumors that start in glial cells. A number of tumors can be considered gliomas, including:
Astrocytomas (which include glioblastomas) Oligodendrogliomas Ependymomas About 3 out of 10 of all brain tumors are gliomas. Most fast-growing brain tumors are gliomas.
Astrocytomas Astrocytomas are tumors that start in glial cells called astrocytes. About 2 out of 10 brain tumors are astrocytomas.
Most astrocytomas can spread widely throughout the brain and blend with the normal brain tissue, which can make them very hard to remove with surgery. Sometimes they spread along the cerebrospinal fluid (CSF) pathways. It is very rare for them to spread outside of the brain or spinal cord.
Astrocytomas (like other brain tumors) are classified into 4 grades.
Non-infiltrating (grade I) astrocytomas do not usually grow into nearby tissues and tend to have a good prognosis. These include pilocytic astrocytomas and subependymal giant cell astrocytomas (SEGAs). They are more common in children than in adults. Low-grade (grade II) astrocytomas, such as diffuse astrocytomas, tend to be slow growing, but they can grow into nearby areas and can become more aggressive and fast growing over time. Anaplastic (grade III) astrocytomas grow more quickly. Glioblastomas (grade IV) are the fastest growing. These tumors make up more than half of all gliomas and are the most common malignant brain tumors in adults. Oligodendrogliomas These tumors start in brain glial cells called oligodendrocytes. These are grade II tumors that tend to grow slowly. Most of these can grow into (infiltrate) nearby brain tissue and cannot be removed completely by surgery. Oligodendrogliomas sometimes spread along the CSF pathways but rarely spread outside the brain or spinal cord. As with astrocytomas, they can become more aggressive over time. Very aggressive (grade III) forms of these tumors are known as anaplastic oligodendrogliomas. Only about 2% of brain tumors are oligodendrogliomas.
Ependymomas These tumors start in ependymal cells, which line the ventricles. They can range from fairly low-grade (grade II) tumors to higher grade (grade III) tumors, which are called anaplastic ependymomas. Only about 2% of brain tumors are ependymomas.
Ependymomas are more likely to spread along the cerebrospinal fluid (CSF) pathways than other gliomas but do not spread outside the brain or spinal cord. Ependymomas may block the exit of CSF from the ventricles, causing the ventricles to become very large – a condition called hydrocephalus.
Unlike astrocytomas and oligodendrogliomas, ependymomas usually do not grow into normal brain tissue. As a result, some (but not all) ependymomas can be removed completely and cured by surgery. But because they can spread along ependymal surfaces and CSF pathways, treating them can sometimes be difficult. Spinal cord ependymomas have the greatest chance of being cured with surgery, but treatment can cause side effects related to nerve damage.
Meningiomas Meningiomas begin in the meninges, the layers of tissue that surround the outer part of the brain and spinal cord. Meningiomas account for about 1 out of 3 primary brain and spinal cord tumors. They are the most common brain tumors in adults (although strictly speaking, they are not actually brain tumors).
The risk of these tumors increases with age. They occur about twice as often in women. Sometimes these tumors run in families, especially in those with neurofibromatosis, a syndrome in which people develop many benign tumors of nerve tissue.
Meningiomas are often assigned a grade, based on how the cells look under the microscope.
Grade I (benign) meningiomas have cells that look the most like normal cells. They account for about 8 of 10 meningiomas. Most of these can be cured by surgery, but some grow very close to vital structures in the brain or cranial nerves and cannot be cured by surgery alone. Grade II (atypical or invasive) meningiomas usually have cells that look slightly more abnormal. They make up about 15% to 20% of meningiomas. They can grow directly into nearby brain tissue and bone and are more likely to come back (recur) after surgery. Grade III (anaplastic or malignant) meningiomas have cells that look the most abnormal. They make up only about 1% to 3% of meningiomas. They tend to grow quickly, can grow into nearby brain tissue and bone, and are the most likely to come back after treatment. Some may even spread to other parts of the body. Medulloblastomas Medulloblastomas develop from neuroectodermal cells (early forms of nerve cells) in the cerebellum. They are fast-growing (grade IV) tumors and often spread throughout the CSF pathways, but they can be treated by surgery, radiation therapy, and chemotherapy.
Medulloblastomas occur much more often in children than in adults. They are part of a class of tumors called embryonal tumors that can also start in other parts of the central nervous system. They are discussed in more detail in Brain and Spinal Cord Tumors in Children.
Gangliogliomas Gangliogliomas contain both neurons and glial cells. These tumors are very uncommon in adults. They are typically slow growing (grade II) tumors and can usually be cured by surgery alone or surgery combined with radiation therapy.
Schwannomas (neurilemmomas) Schwannomas develop from Schwann cells, which surround and insulate cranial nerves and other nerves. They make up about 8% of all CNS tumors.
Schwannomas are almost always benign (grade I) tumors. They can arise from any cranial nerve. When they form on the cranial nerve responsible for hearing and balance near the cerebellum they are called vestibular schwannomas or acoustic neuromas. They can also start on spinal nerves after the point where they have left the spinal cord. When this happens, they can press on the spinal cord, causing weakness, sensory loss, and bowel and bladder problems.
Craniopharyngiomas These slow-growing (grade I) tumors start above the pituitary gland but below the brain itself. They may press on the pituitary gland and the hypothalamus, causing hormone problems. Because they start very close to the optic nerves, they can also cause vision problems. Their tendency to stick to these important structures can make them hard to remove completely without damaging vision or hormone balance. Craniopharyngiomas are more common in children, but they are sometimes seen in adults.
Other tumors that can start in or near the brain Chordomas These rare tumors start in the bone at the base of the skull or at the lower end of the spine. Chordomas don’t start in the central nervous system, but they can injure the nearby brain or spinal cord by pressing on it.
These tumors are treated with surgery if possible, often followed by radiation therapy, but they tend to come back in the same area after treatment, causing more damage. They usually do not spread to other organs. For more information on chordomas, see Bone Cancer.
Non-Hodgkin lymphomas Lymphomas are cancers that start in white blood cells called lymphocytes (one of the main cell types of the immune system). Most lymphomas start in other parts of the body, but some start in the CNS, and are called primary CNS lymphomas. These lymphomas are more common in people with immune system problems, such as those infected with HIV, the virus that causes AIDS. Because of new treatments for AIDS, primary CNS lymphomas have become less common in recent years.
These lymphomas often grow quickly and can be hard to treat. Recent advances in chemotherapy, however, have improved the outlook for people with these cancers. For more information on primary CNS lymphomas (including treatment), see Non-Hodgkin Lymphoma.
Pituitary tumors Tumors that start in the pituitary gland are almost always benign (non-cancerous). But they can still cause problems if they grow large enough to press on nearby structures or if they make too much of any kind of hormone. For more information, see Pituitary Tumors.
Written by References
See also
Where to find medical care for oligodendroglioma?
Directions to Hospitals Treating oligodendroglioma
Sources
https://www.cancer.org/cancer/brain-spinal-cord-tumors-adults/about/types-of-brain-tumors.html