大炎性肌瘤息肉继发空肠肠套叠1例及鉴别诊断探讨。

IF 0.7 Q4 PATHOLOGY
Asma Khalid Abu-Salah, Eric Brocken, Hector Mesa, Katrina Collins
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引用次数: 0

摘要

炎性肌瘤息肉(IFP)最初被认为是一种反应性过程,现在被认为是一种良性胃肠道间质肿瘤。我们报告一例68岁妇女难治性克罗恩病,表现为肠套叠需要手术干预。切除显示空肠肿块,包括粘膜下无色素梭形细胞增生的纤维间质,并有大量嗜酸性粒细胞浸润。免疫组化结果显示,vimentin阳性,desmin、平滑肌肌动蛋白(SMA)、S-100、CD117、DOG1、ALK (D5F3)、Melan-A、HMB-45、CD34、STAT6阴性。Ki-67增殖指数低(
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Jejunal Intussusception Secondary to a Large Inflammatory Fibroid Polyp: A Case Report and Discussion of Differential Diagnosis.

Inflammatory fibroid polyp (IFP), initially considered a reactive process, is now recognized as a benign mesenchymal neoplasm of the gastrointestinal tract. We report a case of a 68-year-old woman with medically refractory Crohn disease that presented with intussusception requiring surgical intervention. The resection revealed a jejunal mass consisting of a submucosal proliferation of bland spindle cells in a fibrous stroma infiltrated by numerous eosinophils. By immunohistochemistry, the lesion was positive for vimentin and negative for desmin, smooth muscle actin (SMA), S-100, CD117, DOG1, ALK (D5F3), Melan-A, HMB-45, CD34, and STAT6. Ki-67 proliferative index was low (<1%). The mass was classified as IFP by its characteristic morphology and associated eosinophilia. IFP should be considered in the differential diagnosis of adults with intussusception or bowel obstruction. Definitive treatment typically requires surgical resection of the involved bowel segment.

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