Multiple Small Bowel Gastrointestinal Stromal Tumors Associated with Neurofibromatosis Type 1 that Were Not Detected by Endoscopy: A Case Report.

IF 0.5 Q4 GASTROENTEROLOGY & HEPATOLOGY
Case Reports in Gastroenterology Pub Date : 2023-03-08 eCollection Date: 2023-01-01 DOI:10.1159/000529340
Satomi Saito, Teppei Omori, Shun Murasugi, Maria Yonezawa, Yukiko Takayama, Takeshi Ohki, Hiromi Onizuka, Yoji Nagashima, Katsutoshi Tokushige
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引用次数: 0

Abstract

We treated a 39-year-old Japanese man who was admitted for an abdominal mass. He had had neurofibroma-like skin lesions since childhood. Computed tomography and endoscopic ultrasound results were consistent with a tumor in the small intestine. Although the tumor was undetectable by single-balloon endoscopy, the patient's background and imaging results led us to suspect a gastrointestinal stromal tumor (GIST). He also met the diagnostic criteria for neurofibroma type 1 (NF1). We performed a surgical removal of the tumor, and the biopsy results led to a definitive diagnosis of GIST. Small bowel GISTs should be considered in cases of NF1.

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内镜检查未发现的与神经纤维瘤病 1 型相关的多发性小肠胃肠道间质瘤:病例报告。
我们收治了一名因腹部肿块入院的 39 岁日本男子。他从小就有神经纤维瘤样皮肤病变。计算机断层扫描和内窥镜超声检查结果与小肠肿瘤一致。虽然单球囊内镜检查无法检测到肿瘤,但患者的背景和成像结果让我们怀疑是胃肠道间质瘤(GIST)。他还符合 1 型神经纤维瘤(NF1)的诊断标准。我们对肿瘤进行了手术切除,活检结果明确诊断为 GIST。NF1病例应考虑小肠GIST。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Case Reports in Gastroenterology
Case Reports in Gastroenterology Medicine-Gastroenterology
CiteScore
1.10
自引率
0.00%
发文量
99
审稿时长
7 weeks
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