Crohn's disease associated with Takayasu arteritis: Case report

Maria Luiza de Andrade , Vivian de Souza Menegassi , Monique Kowalski Schmitz , Camila Marques de Valois Lanzarin
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Abstract

Crohn's disease (CD) and Takayasu's arteritis (TA) are both chronic, granulomatous, autoimmune diseases, and their coexistence is extremely rare. This report describes the case of an adolescent diagnosed with CD who developed vasculitis affecting the aorta and major branches, leading to TA. The case highlights the clinical findings that led to the diagnosis and the therapy used. Additionally, it underscores the importance of considering vasculitis, most commonly TA, in patients with CD who present with thrombotic events and elevated inflammatory markers, even in the absence of gastrointestinal symptoms. Early diagnosis enables timely initiation of appropriate treatment to improve outcomes.
克罗恩病合并高须动脉炎1例报告
克罗恩病(CD)和Takayasu动脉炎(TA)都是慢性肉芽肿性自身免疫性疾病,两者共存极为罕见。本报告描述了一个被诊断为乳糜泻的青少年,他发展为影响主动脉和主要分支的血管炎,导致TA。该病例强调了导致诊断和使用治疗的临床发现。此外,它强调了考虑血管炎的重要性,最常见的是TA,在出现血栓事件和炎症标志物升高的乳糜泻患者中,即使没有胃肠道症状。早期诊断可以及时开始适当的治疗,以改善结果。
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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