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for pediatric brain tumors

Once a diagnosis has been made, doctors will then decide on a treatment plan. It may range from observation (no need for immediate therapy at all) to a combination of surgery (in which the tumor is physically removed during a surgical procedure), radiation therapy (which uses high-energy particles or waves, such as x-rays, to destroy or damage cancer cells), and aggressive chemotherapy (which uses drugs to treat the tumor). Your child's chance of recovery depends on a number of factors, including tumor type and location, and amount of tumor spread, or metastasis, but it's important to note that there are treatments available for every type of brain tumor.

Tumors that form in the tissues and cells of a child's brain are called primary brain tumors. In some cases, tumors that have originated in other parts of the body spread to the brain, but this is rare in children. The following is a list of some of the most common types of primary brain tumors found in children.

Astrocytomas (also known as gliomas)

Accounting for almost half of all childhood brain tumors, astrocytomas are tumors that arise in brain cells called astrocytes (astrocytes are star shaped cells in the central nervous system that support neurons and help remove debris). Astrocytomas can be further divided into the following types:

  • Low-grade astrocytomas, which include Grade 1 (Juvenile pilocytic astrocytomas) and Grade 2 (Fibrillary astrocytomas) astrocytomas. They may be cured with surgery alone if they can be completely removed. If not, observation only may be considered. If additional treatment is required, radiation therapy is usually used for the older children and chemotherapy is used for the younger children.

  • High-grade astrocytomas include Grade 3 (Anaplastic astrocytomas) and Grade 4 (Glioblastoma multiforme) astrocytomas. They are highly malignant tumors that have a much more guarded prognosis. Surgery, radiation therapy, and chemotherapy are usually recommended.

Also, diffuse pontine gliomas (a type of brain stem glioma) are highly malignant astrocytomas that occur in a very delicate part of the brain. Surgery cannot be done safely, and patients are usually treated with radiation therapy and may be candidates for new investigational treatments. Prognosis is very guarded.

Ependymomas

Ependymomas develop within the ependymal cells lining the brain's ventricles (a series of fluid filled cavities in the brain) and are treated with surgical resection and often with radiation therapy. Ependymomas, unlike astrocytomas, typically do not spread into normal, surrounding brain tissue. Children who have ependymomas that cannot be completely resected are often also treated with chemotherapy. Though there are no treatments unique to ependymomas, radiation therapy is an extremely important part of the typical treatment plan, often including the use of intensity modulated radiation therapy (IMRT) -- a targeted treatment that delivers high-doses of radiation to tumor cells while sparing surrounding healthy tissue.

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Medulloblastomas and PNETs

Representing approximately 15 percent of childhood brain tumors, medulloblastomas are tumors that, doctors think, arise from undeveloped stem cells in the portion of the brain that controls voluntary movement, the cerebellum. They are highly malignant, but with appropriate treatment many children can be cured. Medulloblastomas usually are accompanied by headaches and vomiting (particularly first thing in the morning). Sometimes the child will show behavioral changes and deterioration of their school performance. The diagnosis is suspected using CT (computed tomography) or MRI (magnetic resonance imaging) scan and confirmed by a pathology examination after the tumor's surgical removal. Treatment for medulloblastomas usually includes surgery, radiation therapy (except in the very young), and chemotherapy. Our investigators have developed a new treatment called radioimmunotherapy in conjunction with a decreased radiation dose (in an attempt to reduce side effects) and conventional chemotherapy.

Primitive neuroectodermal tumors (PNET) are another form of rapidly growing tumor that are known as pineoblastomas when they occur in the pineal gland (a pea-sized gland at the center of the brain), and supratentorial PNETs when occurring in the cerebral hemispheres. The diagnosis is suspected via CT or MRI scan and confirmed by pathology after the tumor's surgical removal. PNETs can prove less responsive to therapies, but treatments are available.

Germ Cell Tumors

Germ cell tumors, as the name suggests, arise from germ cells, which during normal development of the embryo form into either egg cells or sperm cells. In the case of germ cell tumors located in the brain, the embryonic germ cells have mistakenly traveled to the brain, where they develop into tumors. Occurring most frequently in children, germ cell tumors comprise several different types of tumors (including germinomas, endodermal sinus tumors, and choriocarcinomas). Though their symptoms depend on the tumor location, germ cell tumors in the pineal region usually are accompanied by headaches and vomiting (particularly first thing in the morning). Tumors in the suprasellar region (near the pituitary gland) usually are accompanied by hormonal abnormalities, particularly increased urination, and thirst. Sometimes the child will show behavioral changes and deterioration of their school performance. Most of them are malignant tumors, but can often be cured with current treatments that may include surgery, radiation therapy, and chemotherapy.

Young Children and Brain Tumors

Young children (those less than three years old) with brain tumors are a special group. Regardless of the type of tumor, we often try to avoid radiation therapy due to the risk of causing learning and memory problems in this age group. Chemotherapy is more frequently recommended.


Last Updated: Jan. 23, 2006
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