Medulloblastoma natural history: Difference between revisions
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{{Medulloblastoma}} | {{Medulloblastoma}} | ||
{{CMG}} | {{CMG}} {{AE}}{{HL}} | ||
==Overview== | ==Overview== | ||
==Natural History== | ==Natural History== |
Revision as of 23:35, 28 September 2015
Medulloblastoma Microchapters |
Diagnosis |
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Treatment |
Case studies |
Medulloblastoma natural history On the Web |
American Roentgen Ray Society Images of Medulloblastoma natural history |
Risk calculators and risk factors for Medulloblastoma natural history |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Haytham Allaham, M.D. [2]
Overview
Natural History
Complications
Prognosis
Treatment begins with maximal resection of the tumor. The addition of radiation to the entire neuraxis and chemotherapy may increase the disease-free survival. This combination may permit a 5 year survival in more than 80% of cases. The presence of desmoplastic features such as connective tissue formation offers a better prognosis. Prognosis is worse if child is less than 3 years old, inadequate degree of resection, or if presence of any CSF, spinal, supratentorial or systemic spread.
Increase intracranial pressure may be controlled with corticosteroids or a ventriculoperitoneal shunt