A rare Von Hippel–Lindau disease that mimics acute myelitis: case report and review of the literatureReportar como inadecuado




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Neurological Sciences

, Volume 32, Issue 2, pp 305–307

First Online: 07 October 2010Received: 03 November 2009Accepted: 01 September 2010

Abstract

Von Hippel–Lindau disease VHL comprises a series of complicated clinical manifestations. We hereby report one unique case of VHL with a natural history that mimics acute myelitis. MRI and biopsy in this patient showed multiple solid hemangioblastomas of the central nervous system and kidney. This study further confirmed that VHL is of highly clinical, imaging, and pathological heterogeneity. Diagnosis for VHL should be based on combination of clinical, radiological, pathological, and genetic data.

KeywordsVon Hippel–Lindau disease Hemangioblastoma Clinical manifestation Magnetic resonance image Histopathology H. Jiang and Y. Shi contributed equally to this work.

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Autor: Hong Jiang - Yu-ting Shi - Jun-ling Wang - Bei-sha Tang - Jun-yu Wang - Ze-feng Peng - De-sheng Xiao

Fuente: https://link.springer.com/







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