Author(s)

Ibrahima Berete^1*, Alpha Boubacar Bah¹, Seylan Diawara¹, Hammas Nawal², Mohammed Benzagmout³, Khalid Chakour³, Mohammed Faiz Chaoui³

¹Department of Neurosurgery, University Hospital Donka, Conakry, Guinea.
²Department of Pathology, University Hospital Hassan II, Fez, Morocco.
³Department of Neurosurgery, University Hospital Hassan II, Fez, Morocco.

Lipomatous medulloblastoma is not a separate entity but apparently distinct variant of medulloblastoma. Since the first case report in 1978 by Bechtel et al. [1], few cases have been published. We report an additional case of a 52-year-old right-handed man presented to the emergency department with evaluation of progressive severe intracranial hypertension and ataxia. His past medical history was unremarkable. His physical examination showed cerebellar syndromes. He underwent magnetic resonance imaging (MRI) which revealed a unique mass in the posterior fossa, lying within a cerebellar hemisphere. The patient underwent a suboccipital craniotomy for with a complete resection and samples were sent for histologic examination, showing closely packed, and round to oval cells. The nuclei had an irregular shape with clumps of heterochromatin. Lipid accumulation was a prominent feature of neoplastic cells. Postoperatively the patient did not receive fractionated radiotherapy. He is alive without deficit and with no evidence of recurrence on neuroimaging.

Medulloblastoma, Lipomatous, Liponeurocytoma, Posterior Fossa, Tumor, Suboccipital Craniotomy

Berete, I. , Bah, A. , Diawara, S. , Nawal, H. , Benzagmout, M. , Chakour, K. and Chaoui, M. (2019) Lipomatous Medulloblastoma: A Case Report. Open Journal of Modern Neurosurgery, 9, 452-456. doi: 10.4236/ojmn.2019.94043.