嗜酸性肉芽肿病合并多血管炎累及胃肠道及治疗反应的组织学证据。

IF 0.5 Q4 GASTROENTEROLOGY & HEPATOLOGY

Case Reports in Gastroenterology Pub Date : 2023-01-01 DOI:10.1159/000529671

Mark Lai, Tony He, Emily K Wright

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引用次数: 0

摘要

嗜酸性肉芽肿病合并多血管炎(EGPA)是一种罕见的小到中等血管的系统性血管炎。累及胃肠道并不常见，且与较高的死亡率相关。治疗基于经验证据。在这篇文章中，我们报告了一例egpa相关的全结肠炎和狭窄性小肠疾病，mepolizumab和手术切除联合治疗。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Gastrointestinal Involvement of Eosinophilic Granulomatosis with Polyangiitis with Histological Evidence of Treatment Response.

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Gastrointestinal Involvement of Eosinophilic Granulomatosis with Polyangiitis with Histological Evidence of Treatment Response.

Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare systemic vasculitis of small to medium vessels. Gastrointestinal involvement is uncommon and is associated with higher mortality. Treatment is based on empiric evidence. In this article, we report a case of EGPA-related pancolitis and stricturing small bowel disease managed with a combination of mepolizumab and surgical resection.

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来源期刊

Case Reports in Gastroenterology Medicine-Gastroenterology

CiteScore

1.10

自引率

0.00%

发文量

审稿时长

7 weeks

期刊介绍：