Subependymal giant cell astrocytoma
| Subependymal giant cell astrocytoma | |
|---|---|
| File:SEGA GFAP x100.jpg
GFAP stained microscopic section of a subependymal giant cell astrocytoma
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| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| ICD-10 | GroupMajor.minor |
| ICD-9-CM | xxx |
| Patient UK | Subependymal giant cell astrocytoma |
Subependymal giant cell astrocytoma (SEGA, SGCA, or SGCT) is a low-grade astrocytic brain tumor (astrocytoma) that arises within the ventricles of the brain.[1] It is most commonly associated with tuberous sclerosis complex (TSC). Although it is a low-grade tumor, its location can potentially obstruct the ventricles and lead to hydrocephalus.
Contents
Symptoms
Individuals with this type of tumor may have no symptoms if cerebrospinal fluid (CSF) flow remains open. Obstruction of CSF flow will result in the symptoms associated with increased CSF pressure: nausea, vomiting, headache (often positional), lethargy, blurry or double vision, new or worsened seizures, and personality change.[2]
Diagnosis
Diagnosis is made by imaging with a contrast-enhanced MRI or CT scan of the brain.
Screening
It is recommended that children with TSC be screened for SEGA with neuroimaging every 1–3 years.[1]
Treatment
Pharmacotherapy
Two related drugs have been shown to shrink or stabilize subependymal giant cell tumors: rapamycin and everolimus. These both belong to the mTOR inhibitor class of immunosuppressants, and are both contraindicated in patients with severe infections.
Rapamycin showed efficacy in five cases of SEGA in TSC patients, shrinking their tumor volumes by an average of 65%. However, after the drug was stopped, the tumors regrew.
Everolimus, which has a similar structure as rapamycin, but with slightly increased bioavailability and shorter half-life, was studied in 28 patients with SEGA. There was a significant reduction in SEGA size in 75% of the patients, and a mild improvement in their seizures. Everolimus was approved for the treatment of SEGA by the US Food and Drug Administration (FDA) in October, 2010.[1]
Surgery
A NIH Consensus Conference report in 1999 recommends that any SEGA that is growing or causing symptoms should be surgically removed.[2] Tumors are also removed in cases where a patient is suffering from a high seizure burden.[1] If a tumor is rapidly growing or causing symptoms of hydrocephalus, deferring surgery may lead to vision loss, need for ventricular shunt, and ultimately death. Total removal of the tumor is curative.
Surgery to remove intraventricular tumors also carries risks of complications or death. Potential complications include transient memory impairment, hemiparesis, infection, chronic ventriculoperitoneal shunt placement, stroke, and death.[1]
Prognosis
After complete surgical removal, a SEGA tumor does not grow back. They do not metastasize to other parts of the body. However, the patient is still at risk for, and often develops, new tumors arising from subependymal nodules elsewhere in the ventricular system.
Epidemiology
SEGAs arise in 5-20% of TSC patients.[1]
