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经直肠结肠切除术治疗药物难治性结肠克罗恩病后出现的皮肤克罗恩病:病例系列及文献综述

Cutaneous Crohn's disease after proctocolectomy for medically refractory colonic Crohn's disease: a case series and review of the literature.

作者信息

Naffouj Sandra, Marrero-Rivera Gabriel E, Nordenstam Johan, Amber Kyle T, Trivedi Itishree

机构信息

Division of Gastroenterology and Hepatology, Department of Medicine, University of Illinois Chicago, IL (Sandra Naffouj, Itishree Trivedi).

Department of Medicine, University of Illinois Chicago, IL (Gabriel E. Marrero-Rivera).

出版信息

Ann Gastroenterol. 2023 Jul-Aug;36(4):466-476. doi: 10.20524/aog.2023.0811. Epub 2023 May 30.

Abstract

BACKGROUND

Cutaneous Crohn's disease (CCD), also known as metastatic Crohn's disease (CD), is one of the rarest and most challenging cutaneous manifestations of CD. It is characterized by non-caseating granulomatous inflammation of the skin at sites that are non-contiguous with the gastrointestinal (GI) tract. Diagnosis of CCD needs a high clinical suspicion since morphological presentation varies widely and lacks an apparent correlation to the activity of the luminal CD. The onset of CCD in patients without active GI CD is a particularly understudied phenomenon.

METHODS

We present a case series of a unique patient group who developed CCD while in remission from a luminal CD perspective, mainly after a proctocolectomy for Crohn's colitis. We also provide a literature review and summary of case reports of CCD after proctocolectomy.

RESULTS

Our 4 adult patients diagnosed with CCD after proctocolectomy presented herein, were successfully treated with high-dose corticosteroids, followed by biologic therapy. Furthermore, a comprehensive review of CCD is provided regarding its pathogenesis, clinical presentation, differential diagnosis, and the evidence behind the available treatments.

CONCLUSIONS

CCD should be considered in any CD patient presenting with skin lesions regardless of their disease activity status and history of proctocolectomy. The treatment remains challenging; biologics remain the cornerstone and a multidisciplinary approach is recommended. Larger randomized clinical trials are essential to determine the optimal treatment protocol and to improve outcomes.

摘要

背景

皮肤克罗恩病(CCD),也称为转移性克罗恩病(CD),是克罗恩病最罕见且最具挑战性的皮肤表现之一。其特征是在与胃肠道(GI)不连续的部位出现皮肤非干酪样肉芽肿性炎症。由于其形态学表现差异很大且与肠腔内CD的活动缺乏明显相关性,因此CCD的诊断需要高度的临床怀疑。在无活动性胃肠道CD的患者中发生CCD这一现象尤其缺乏研究。

方法

我们报告了一组独特患者的病例系列,这些患者从肠腔内CD的角度来看处于缓解期时发生了CCD,主要是在因克罗恩结肠炎行直肠结肠切除术后。我们还提供了文献综述以及直肠结肠切除术后CCD病例报告的总结。

结果

本文介绍的4例成年患者在直肠结肠切除术后被诊断为CCD,他们成功接受了高剂量皮质类固醇治疗,随后进行了生物治疗。此外,还提供了关于CCD的发病机制、临床表现、鉴别诊断以及现有治疗方法背后证据的全面综述。

结论

任何出现皮肤病变的CD患者,无论其疾病活动状态和直肠结肠切除术病史如何,都应考虑CCD。治疗仍然具有挑战性;生物制剂仍然是基石,建议采用多学科方法。更大规模的随机临床试验对于确定最佳治疗方案和改善治疗结果至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a7e/10304526/aa7b3dd473d6/AnnGastroenterol-36-466-g003.jpg

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