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脊髄血管芽腫・褐色細胞腫・多発膵腫瘍を合併したvon Hippel-Lindau病の1例

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This article is published in The Japanese Journal of Gastroenterological Surgery.The article was published on 2017-07-01 and is currently open access. It has received 0 citations till now.

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Journal ArticleDOI

von Hippel-Lindau disease

TL;DR: An overview of the clinical aspects, management, and treatment options for von Hippel-Lindau disease is presented.
Journal ArticleDOI

Pancreatic involvement in von Hippel–Lindau disease

TL;DR: Pancreatic involvement is seen in most patients with VHL disease, and specific treatment of pancreatic lesions is required in selected patients, mainly those with neuroendocrine tumors.
Journal ArticleDOI

Von Hippel-Lindau Disease: Clinical and Pathological Manifestations in Nine Families With 50 Affected Members

TL;DR: Cerebellar hemangioblastoma, which is observed in one third of patients, is the most common source of initial symptoms and caused more than half of the deaths in the series.
Journal ArticleDOI

Clinical, genetic and radiographic analysis of 108 patients with von Hippel-Lindau disease (VHL) manifested by pancreatic neuroendocrine neoplasms (PNETs).

TL;DR: By implementing a system of selective operative resection based on defined criteria, vHL patients with PNETs can be managed safely and a nonoperative approach may be appropriate for these nonfunctional neoplasms.
Journal ArticleDOI

Pancreatic lesions in von Hippel-Lindau disease: prevalence, clinical significance, and CT findings.

TL;DR: Pancreatic lesions, including cysts, may precede any other manifestation of von Hippel-Lindau disease by several years, and recognition permits earlier diagnosis in patients being screened for von Hippenau disease.
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