Many of us remember medulloblastoma as the proto-type malignant childhood brain tumor we learned about in medical school [1]. Typically, a child aged approximately 5 years presents with several weeks to months of nausea, vomiting, headaches, ataxia, and sometimes a turned-in eye or abducens nerve paresis. Subsequent head computed to-mography or magnetic resonance imaging reveals a some-what circumscribed cerebellar tumor and obstructive hy-drocephalus. Histologically, the WHO defines this small, round, blue-cell tumor with hyperchromatic nuclei and scant cytoplasm as a grade 4 neoplasm [2]. Because of its tendency to disseminate through the subarachnoid spaces and to form microscopic or bulky metastases in about a third of patients, craniospinal radiotherapy to a dosage of 36 Gy, with an additional radiation boost to the posterior
No takes yet. Share an insight, caveat, or question.
Fisher et al. (2004) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: