Abstract
The purpose of this study was to emphasize that cerebellar glioblastoma multiforme, although quite rare, should be included in the differential diagnosis of tumors of the posterior cranial fossa in adults. The cerebellum has been known to be the site of predilection of hemangioblastoma, medulloblastoma, metastasis, and pilocytic astrocytoma. Very few adult cerebellar glioblastoma have been reported previously. We present a case and discuss the neuroradiologic and pathologic features of this interesting location of these highly malignant tumors, which are diagnosed radiologically to be meningioma, hemangioblastoma, or metastasis. In the present case, a solitary mass was detected and interpreted as a meningioma on a magnetic resonance image (MRI) with gadolinium. Repeated follow-up studies and histologic confirmation by image-guided stereotactic biopsy were important for the diagnosis, since glioblastoma was unsuspected at the onset. Establishment of the cell of origin is of critical importance for planning therapy and prognostication. The absence of what today is considered evidence-based medicine to treat high-grade gliomas, coupled with the rare occurrence at this location, indicates that cerebellar glioblastoma has to be differentiated from other tumors without delay upon radiologic diagnosis.
Keywords: Cerebellar glioblastoma; Treatment modalities; Prognostic factors; Outcome
Copyright © 2020 by The American Society for BioMedicine and BM-Publisher, Inc.
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