Multiple gastrointestinal stromal tumors and bilateral pheochromocytoma in neurofibromatosis

被引:33
作者
Kramer, Klaus
Hasel, Cornelia
Aschoff, Andrik J.
Henne-Bruns, Doris
Wuerl, Peter
机构
[1] Univ Hosp Ulm, Dept Gen Visceral & Transplant Surg, D-89077 Ulm, Germany
[2] Univ Hosp Ulm, Dept Surg, D-89077 Ulm, Germany
[3] Univ Hosp Ulm, Dept Pathol, D-89077 Ulm, Germany
[4] Univ Hosp Ulm, Dept Diagnost & Intervent Rad, D-89077 Ulm, Germany
关键词
gastrointestinal stromal tumor; neuroendocrine tumor; neurofibromatosis; pheochromocytoma; coincidence;
D O I
10.3748/wjg.v13.i24.3384
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The coincidence of a gastrointestinal stromal tumor (GIST) and a neuroendocrine tumor (NET) in neurofibromatosis type 1 (NF1) is described only five times within the literature. We report on a 63 year old Caucasian female with the rare condition of neurofibromatosis type 1 coinciding with recurrent gastrointestinal stromal tumor plus bilateral pheochromocytoma (PCC). After a history of palpitations and dizziness that lasted for years, a left adrenal mass was detected by CT. Laparotomy revealed a pheochromocytoma of the left adrenal gland while an ileoterminal GIST was found incidentally intraoperatively. After six months contralateral PCC and multiple recurrent GIST were resected again. After four years the patient is doing well without any signs of further recurrent tumors. Discussion includes review of the literature. (c) 2007 The WJG Press. All rights reserved.
引用
收藏
页码:3384 / 3387
页数:4
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