Two-stage resection of a bilateral pheochromocytoma and pancreatic neuroendocrine tumor in a patient with von Hippel-Lindau disease: A case report

INTRODUCTION: von Hippel-Lindau disease (vHL disease) is a hereditary disease in which tumors and cysts develop in many organs, in association with central nervous system hemangioblastomas, pheochromocytomas, and pancreatic tumors. We herein report a case of vHL disease (type 2A) associated with bil...

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Publié dans:Int J Surg Case Rep
Auteurs principaux: Endo, Yutaka, Kitago, Minoru, Miyajima, Akira, Kurihara, Isao, Kameyama, Kaori, Shinoda, Masahiro, Yagi, Hiroshi, Abe, Yuta, Hibi, Taizo, Takagi, Chisato, Nakano, Yutaka, Koizumi, Wataru, Itano, Osamu, Kitagawa, Yuko
Format: Artigo
Langue:Inglês
Publié: Elsevier 2018
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Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC5910515/
https://ncbi.nlm.nih.gov/pubmed/29501019
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijscr.2018.02.020
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