克罗恩病合并巨囊性微结肠肠蠕动不足综合征1例。

JPGN reports Pub Date : 2025-03-10 eCollection Date: 2025-05-01 DOI:10.1002/jpr3.70015
Caroline Chinchilla Putzeys, Trenton House, Janet Iurilli, Ana Gomez, Shipra Garg, Elisa Wershba, Gary Silber, Mitchell Shub, Dana Williams
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引用次数: 0

摘要

摘要巨囊性微结肠肠蠕动不足症候群(MMIHS)是一种罕见的先天性疾病,其症状为肠道和膀胱假性梗阻。它具有严重的发病率和死亡率;少数患者能活到成年。MMIHS患者反复进行肠道手术、小肠细菌过度生长和肠道运输减慢可能是肠黏膜慢性炎症的潜在危险因素,这与炎症性肠病的风险相关。在本病例报告中,我们详细介绍了一位诊断为MMIHS和炎症性肠病的患者的不寻常表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case of Crohn's disease in a patient with megacystis microcolon intestinal hypoperistalsis syndrome.

Megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS) is a rare congenital condition resulting in symptoms of bowel and bladder pseudo-obstruction. It carries severe morbidity and mortality; a minority of patients survive to adulthood. Recurrent bowel surgeries, small intestinal bacterial overgrowth, and slowed intestinal transit in MMIHS could serve as potential risk factors for chronic inflammation of the intestinal mucosa, which has been associated with risk of inflammatory bowel disease. In this case report, we detail the unusual presentation of a patient diagnosed with both MMIHS and inflammatory bowel disease.

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