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. © 2010 The Author(s).
CITATION STYLE
Jiang, H., Shi, Y. T., Wang, J. L., Tang, B. S., Wang, J. Y., Peng, Z. F., & Xiao, D. S. (2011). A rare von Hippel-Lindau disease that mimics acute myelitis: Case report and review of the literature. Neurological Sciences, 32(2), 305–307. https://doi.org/10.1007/s10072-010-0413-3
Mendeley helps you to discover research relevant for your work.