Islet Cell Tumor in von Hippel-Lindau Disease

Nobumasa Mizlno, Satoru Naruse, Motoji Kitagawa, Hiroshi Ishiguro, Yasuyuki Nakak, Hideaki Ihda, Naohiko Iizuka, Osamu Ito, Yasunaga Seki, Shigeru B.H. Ko, Toshiyuki Yoshikawa, Tetsuo Hayakawa, Tsuyoshi Sano, Junichi Kamiya, Yuji Nimura, Tetsuro Nagasaka

研究成果: Article査読

4 被引用数 (Scopus)

抄録

We describe a 42-year-old man with von Hippel-Lindau disease and islet cell tumor of the pancreas. He had retinal and cerebellar hemangioblastomas. His sister had pheochromocytoma. A pancreatic tumor was detected by ultrasonography at his periodical medical checkup. Contrast enhanced computed tomography and abdominal angiography revealed a hypervascular tumor in the pancreatic head. Histological examination of the resected tumor revealed characteristics of islet cell tumor of the pancreas, which was positive for chromogranin- A, S-100 protein, and pancreatic polypeptide, but was negative for insulin, gastrin, glucagon, somatostatin, vasoactive intestinal peptide, serotonin, and adrenocorticotropic hormone.

本文言語English
ページ(範囲)295-299
ページ数5
ジャーナルInternal Medicine
37
3
DOI
出版ステータスPublished - 1998

ASJC Scopus subject areas

  • 内科学

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