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Jejunitis and brown bowel syndrome with multifocal carcinogenesis of the small bowel

机译:空肠和棕色肠综合征伴小肠多灶癌变

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摘要

This is the first report describing a case where prolonged, severe malabsorption from brown bowel syndrome progressed to multifocally spread small bowel adenocarcinoma. This case involves a female patient who was initially diagnosed with chronic jejunitis associated with primary diffuse lymphangiectasia at the age of 26 years. The course of the disease was clinically, endoscopically, and histologically followed for 21 years until her death at the age 47 due to multifocal, metastasizing adenocarcinoma of the small bowel. Multiple lipofuscin deposits (so-called brown bowel syndrome) and severe jejunitis were observed microscopically, and sections of the small bowel showed dense lymphoplasmacytic infiltration of the lamina propria as well as blocked lymphatic vessels. After several decades, multifocal nests of adenocarcinoma cells and extensive, flat, neoplastic mucosal proliferations were found only in the small bowel, along with a loss of the mismatch repair protein MLH1 as a long-term consequence of chronic jejunitis with malabsorption. No evidence was found for hereditary nonpolyposis colon carcinoma syndrome. This article demonstrates for the first time multifocal carcinogenesis in the small bowel in a malabsorption syndrome in an enteritis-dysplasia-carcinoma sequence.
机译:这是第一份报告,描述了由棕色肠综合征引起的长期严重吸收不良发展为多灶性扩散的小肠腺癌的病例。该病例涉及一名女性患者,该患者最初在26岁时被诊断为伴有原发性弥漫性淋巴管扩张的慢性空肠炎。该疾病的病程在临床,内窥镜和组织学方面进行了21年随访,直到她因多灶性转移性小肠腺癌去世,享年47岁。显微镜下观察到多个脂褐素沉积物(所谓的棕色肠综合症)和严重的空肠炎,小肠的切片显示固有层的致密淋巴浆细胞性浸润以及淋巴管阻塞。几十年后,仅在小肠中发现了腺癌细胞的多灶巢和广泛,扁平的赘生性粘膜增生,以及失配修复蛋白MLH1的丧失是慢性空肠炎吸收不良的长期后果。没有发现遗传性非息肉性结肠癌综合征的证据。本文首次证明了肠炎-增生-癌序列中吸收不良综合征的小肠多灶性癌变。

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