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一名患有冯·雷克林豪森病患者的十二指肠中生长抑素瘤与胃肠道间质瘤并存

The Coexistence of Somatostatinoma and Gastrointestinal Stromal Tumor in the Duodenum of a Patient with Von Recklinghausen's Disease.

作者信息

Yamamoto Ryuichi, Kato Shingo, Maru Toshinori, Ninomiya Riki, Ozawa Fumiaki, Beck Yoshifumi, Abe Keiko, Tamaru Jun-Ichi, Nagoshi Sumiko, Yakabi Koji

机构信息

Department of Gastroenterology and Hepatology, Saitama Medical Center, Saitama Medical University, Japan.

出版信息

Intern Med. 2016;55(6):617-22. doi: 10.2169/internalmedicine.55.5761. Epub 2016 Mar 15.

DOI:10.2169/internalmedicine.55.5761
PMID:26984078
Abstract

We herein describe a case of somatostatinoma coexisting with a gastrointestinal stromal tumor (GIST) in the duodenum of an 81-year-old woman with Von Recklinghausen's disease (VRD) and common bile duct stone who presented with diarrhea of three months in duration. Gastroduodenoscopy revealed an ulcer on the second part of the duodenum. A 2.1-cm enhancing tumor was observed to extend from the ulcer on an abdominal computed tomography scan. Subtotal stomach-preserving pancreaticoduodenectomy revealed a somatostatinoma on the papilla of the vater and duodenal GIST. There have been only eight reports on VRD associated with ampullary somatostatinoma and GIST. An awareness of this possibility in patients with gastrointestinal lesions is necessary for proper treatment and patient management.

摘要

我们在此描述了一例81岁患有冯雷克林霍增氏病(VRD)、胆总管结石且持续腹泻三个月的女性十二指肠中生长抑素瘤与胃肠道间质瘤(GIST)共存的病例。胃十二指肠镜检查发现十二指肠第二部有溃疡。腹部计算机断层扫描显示一个2.1厘米的强化肿瘤从溃疡处延伸。保留胃的胰十二指肠次全切除术发现 Vater 乳头处有生长抑素瘤和十二指肠GIST。仅有八篇关于VRD合并壶腹生长抑素瘤和GIST的报告。对于胃肠道病变患者,认识到这种可能性对于正确治疗和患者管理是必要的。

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1
The Coexistence of Somatostatinoma and Gastrointestinal Stromal Tumor in the Duodenum of a Patient with Von Recklinghausen's Disease.一名患有冯·雷克林豪森病患者的十二指肠中生长抑素瘤与胃肠道间质瘤并存
Intern Med. 2016;55(6):617-22. doi: 10.2169/internalmedicine.55.5761. Epub 2016 Mar 15.
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引用本文的文献

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Pancreatic Gastrinoma, Gastrointestinal Stromal Tumor (GIST), Pheochromocytoma, and Hürthle Cell Neoplasm in a Patient with Neurofibromatosis Type 1: A Case Report and Literature Review.1 型神经纤维瘤病患者中的胰腺胃泌素瘤、胃肠道间质瘤(GIST)、嗜铬细胞瘤和 Hurthle 细胞肿瘤:病例报告及文献复习。
Am J Case Rep. 2021 Jan 16;22:e927761. doi: 10.12659/AJCR.927761.
2
Somatostatinoma: Beyond neurofibromatosis type 1 (Review).生长抑素瘤:超越1型神经纤维瘤病(综述)
Exp Ther Med. 2020 Oct;20(4):3383-3388. doi: 10.3892/etm.2020.8965. Epub 2020 Jul 3.
3
Duodenal somatostatinoma presenting as obstructive jaundice with the coexistence of a gastrointestinal stromal tumour in neurofibromatosis type 1: a case with review of the literature.
十二指肠生长抑素瘤表现为梗阻性黄疸并合并1型神经纤维瘤病中的胃肠道间质瘤:1例病例及文献复习
BMJ Case Rep. 2019 Jan 10;12(1):bcr-2018-226702. doi: 10.1136/bcr-2018-226702.
4
Surgical treatment of gastrointestinal stromal tumors of the duodenum: a literature review.十二指肠胃肠道间质瘤的外科治疗:文献综述
Transl Gastroenterol Hepatol. 2018 Sep 21;3:71. doi: 10.21037/tgh.2018.09.04. eCollection 2018.
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Clinicopathological features, surgical strategy and prognosis of duodenal gastrointestinal stromal tumors: a series of 300 patients.十二指肠胃肠道间质瘤的临床病理特征、外科治疗策略和预后:300 例患者系列研究。
BMC Cancer. 2018 May 15;18(1):563. doi: 10.1186/s12885-018-4485-4.
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Intraductal papillary bile duct adenocarcinoma and gastrointestinal stromal tumor in a case of neurofibromatosis type 1.1 型神经纤维瘤病中发生的导管内乳头状胆管腺癌和胃肠道间质瘤。
World J Gastroenterol. 2018 Jan 28;24(4):537-542. doi: 10.3748/wjg.v24.i4.537.