Cerebellar Astrocytomas are one of the more common
pediatric Brain tumors (10%), comprising 27% of pediatric
Posterior Cranial Fossa tumors. They are much less common
in adults. The post-operative survival is longer than other types of
Astrocytomas.
The most frequent and almost universal symptom is
Headache with or without Nausea and Vomiting (these
latter symptoms usually occur later in the course of the
disease when the intracranial pressure is abnormally increased.)
In additional to all of the symptoms present in patients with
increased intracranial pressure, tumors in the Posterior Cranial
Fossa can cause Gait Disturbance, increased Clumsiness as
well as Double Vision (Diplopia.)
MRI Scan is the most reliable and accurate neuroimaging
procedure.
Surgical excision of the maximal amount of the tumor that can
be removed, without producing neurological deficits, is the
appropriate treatment. In tumors composed of a nodule and a cyst,
excision of the nodule is usually definitive therapy. These
patients generally have a high rate of long term (5 to 10 or more
year) survival.
Radiation therapy is not recommended in these cases, since the
complication rates of Radiation Therapy in patients whose expected
survival for 5 or more years, is quite high.
Careful attention to follow up is required using repeat MRI scans.
Repeat operation is appropriate, if there is a recurrence of the
tumor.
Chemotherapy is not appropriate for these tumors since the
lesions are not aggressive and are usually
definitively managed by direct surgical resection.
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This page last edited on 2/19
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