A rare cause of intestinal obstruction: jejunal ALK positive anaplastic large-cell lymphoma.

IF 2.7 4区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Boying Liu, Fu Guan, Shengbing Wang
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引用次数: 0

Abstract

A 32-year-old man had recurrent abdominal pain and vomiting for 2 weeks. Physical examination revealed a 4×2-cm abdominal tough mass with unclear boundaries. Palpation caused mild tenderness without rebound pain. Computed tomography (CT) showed a proximal jejunal mass with incomplete small-bowel obstruction , and double-balloon enteroscopy showed a large protruding proximal jejunal mass covered with dirt and a narrow lumen ; an enteroscope would not pass through. Pathological diagnosis by insufficiently deep endoscopic biopsy is difficult. After multidisciplinary discussion, surgical resection was performed. Histopathology revealed a malignant tumor . Immunohistochemical results: CD30 (+), ALK (+), EMA (+), GrB (+), CD2 (+), CD43 (+), TIA-1 (+), and silver staining (+). Sarcoma 86 fusion-gene detection showed NPM1-ALK gene rearrangement. The patient was diagnosed with anaplastic large-cell lymphoma (ALCL) and underwent chemotherapy.

一罕见的肠梗阻原因:空肠ALK阳性间变性大细胞淋巴瘤。
男,32岁,反复腹痛、呕吐2周。体格检查发现4×2-cm腹部硬块,边界不清。触诊引起轻度压痛,无反跳痛。计算机断层扫描(CT)显示空肠近端肿块伴不完全性小肠梗阻,双球囊肠镜显示空肠近端肿块大而突出,覆盖有污垢和狭窄的管腔;肠镜无法通过。不充分的深内镜活检病理诊断是困难的。经多学科讨论,行手术切除。组织病理学显示为恶性肿瘤。免疫组化结果:CD30(+)、ALK(+)、EMA(+)、GrB(+)、CD2(+)、CD43(+)、TIA-1(+)、银染色(+)。86号肉瘤融合基因检测显示NPM1-ALK基因重排。患者被诊断为间变性大细胞淋巴瘤(ALCL)并接受化疗。
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
CiteScore
2.00
自引率
25.00%
发文量
400
审稿时长
6-12 weeks
期刊介绍: La Revista Española de Enfermedades Digestivas, Órgano Oficial de la Sociedad Española de Patología Digestiva (SEPD), Sociedad Española de Endoscopia Digestiva (SEED) y Asociación Española de Ecografía Digestiva (AEED), publica artículos originales, editoriales, revisiones, casos clínicos, cartas al director, imágenes en patología digestiva, y otros artículos especiales sobre todos los aspectos relativos a las enfermedades digestivas.
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