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

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...

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Detalles Bibliográficos
Autores principales: Jiang, Hong, Shi, Yu-ting, Wang, Jun-ling, Tang, Bei-sha, Wang, Jun-yu, Peng, Ze-feng, Xiao, De-sheng
Formato: Texto
Lenguaje:English
Publicado: Springer Milan 2010
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3056988/
https://www.ncbi.nlm.nih.gov/pubmed/20927563
http://dx.doi.org/10.1007/s10072-010-0413-3
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author Jiang, Hong
Shi, Yu-ting
Wang, Jun-ling
Tang, Bei-sha
Wang, Jun-yu
Peng, Ze-feng
Xiao, De-sheng
author_facet Jiang, Hong
Shi, Yu-ting
Wang, Jun-ling
Tang, Bei-sha
Wang, Jun-yu
Peng, Ze-feng
Xiao, De-sheng
author_sort Jiang, Hong
collection PubMed
description 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.
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spelling pubmed-30569882011-04-05 A rare Von Hippel–Lindau disease that mimics acute myelitis: case report and review of the literature Jiang, Hong Shi, Yu-ting Wang, Jun-ling Tang, Bei-sha Wang, Jun-yu Peng, Ze-feng Xiao, De-sheng Neurol Sci Case Report 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. Springer Milan 2010-10-07 2011 /pmc/articles/PMC3056988/ /pubmed/20927563 http://dx.doi.org/10.1007/s10072-010-0413-3 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Case Report
Jiang, Hong
Shi, Yu-ting
Wang, Jun-ling
Tang, Bei-sha
Wang, Jun-yu
Peng, Ze-feng
Xiao, De-sheng
A rare Von Hippel–Lindau disease that mimics acute myelitis: case report and review of the literature
title A rare Von Hippel–Lindau disease that mimics acute myelitis: case report and review of the literature
title_full A rare Von Hippel–Lindau disease that mimics acute myelitis: case report and review of the literature
title_fullStr A rare Von Hippel–Lindau disease that mimics acute myelitis: case report and review of the literature
title_full_unstemmed A rare Von Hippel–Lindau disease that mimics acute myelitis: case report and review of the literature
title_short A rare Von Hippel–Lindau disease that mimics acute myelitis: case report and review of the literature
title_sort rare von hippel–lindau disease that mimics acute myelitis: case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3056988/
https://www.ncbi.nlm.nih.gov/pubmed/20927563
http://dx.doi.org/10.1007/s10072-010-0413-3
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