Aggressive dissemination of central nervous system hemangioblastoma without association with von Hippel–Lindau disease: A case report and literature review

Author:

Dantas François1,Raso Jair Leopoldo1,Braga Patrícia Salomé Gouvea2,Botelho Ricardo Vieira3,Dantas Fernando Luiz Rolemberg1

Affiliation:

1. Department of Neurosurgery, Nova Lima, Minas Gerais, Brazil,

2. Pathology, Biocor Instituto, Nova Lima, Minas Gerais, Brazil,

3. Department of Neurosurgery, Instituto de Assistência Médica ao Servidor Público do Estado de São Paulo (IAMSPE), São Paulo, São Paulo, Brazil.

Abstract

Background: Hemangioblastomas (HBs) typically present with benign behavior and are most commonly found in the posterior fossa. Multiple central nervous system (CNS) HBs are usually associated with von Hippel–Lindau disease, and leptomeningeal dissemination of sporadic HBs is extremely rare. A review of the literature identified 30 cases of leptomeningeal dissemination of sporadic HBs previously published in the literature. Case Description: We report the case of a patient who was diagnosed with multiple CNS HBs with aggressive progression 6 years after resection of a posterior fossa HB. He underwent multiple surgeries and died 4 years after the diagnosis of the first spinal dissemination. Conclusion: Dissemination of sporadic HBs is rare and aggressive disease evolution is usually observed. Further studies are necessary to determine the optimal therapeutic options.

Publisher

Scientific Scholar

Subject

Neurology (clinical),Surgery

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