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药物性肠-结肠炎与白细胞介素-17 抑制剂的使用有关:胶囊内镜检查结果和病理特征:一例报告。

Drug-induced entero-colitis due to interleukin-17 inhibitor use; capsule endoscopic findings and pathological characteristics: A case report.

机构信息

Department of Gastroenterology, Tsujinaka Hospital Kashiwano-Ha, Kashiwa 277-0871, Japan.

出版信息

World J Gastroenterol. 2023 Aug 28;29(32):4912-4919. doi: 10.3748/wjg.v29.i32.4912.

Abstract

BACKGROUND

Interleukin-17 (IL-17) inhibitors are known to cause exacerbation or new onset of inflammatory bowel disease upon administration. However, few reports have described characteristic endoscopic and histopathologic findings, and no small intestinal lesions have been reported so far.

CASE SUMMARY

A woman in her 60s with psoriasis was administered ixekizumab (IXE), an anti-IL-17A antibody, for the treatment of psoriasis. Twenty months after commencing treatment, the patient visited our hospital because of persistent diarrhea. Blood tests performed at the time of the visit revealed severe inflammation, and colonoscopy revealed multiple round ulcers throughout the colon. A tissue biopsy of the ulcer revealed infiltration of inflammatory cells and granuloma-like findings in the submucosal layer. Capsule endoscopy revealed multiple jejunal erosions. After the withdrawal of IXE, the symptoms gradually improved, and ulcer reduction and scarring of the colon were endoscopically confirmed.

CONCLUSION

To the best of our knowledge, 17 reports have documented IL-17 inhibitor-induced entero-colitis with endoscopic images, endoscopic findings, and pathological characteristics, including the present case. Nine of these cases showed diffuse loss of vascular pattern, coarse mucosa/ulcer formation in the left colon, and endoscopic findings similar to those of ulcerative colitis. In the remaining eight cases, discontinuous erosions and ulcerations from the terminal ileum to the rectum were seen, with endoscopic findings similar to those of Crohn's disease. In this case, the findings were confirmed by capsule endoscopy, which has not been previously reported.

摘要

背景

白细胞介素-17(IL-17)抑制剂在给药后已知会引发炎症性肠病的恶化或新发病例。然而,很少有报道描述其特征性的内镜和组织病理学发现,迄今为止尚未报道小肠病变。

病例总结

一位 60 多岁的银屑病女性患者接受了依奇珠单抗(IXE),一种抗 IL-17A 抗体,用于治疗银屑病。开始治疗 20 个月后,患者因持续性腹泻就诊于我院。就诊时的血液检查显示严重炎症,结肠镜检查显示整个结肠有多个圆形溃疡。溃疡的组织活检显示炎症细胞浸润和黏膜下层的类肉芽肿样表现。胶囊内镜显示多个空肠糜烂。IXE 停药后,症状逐渐改善,结肠镜检查证实结肠溃疡减少和瘢痕形成。

结论

据我们所知,已有 17 份报告记录了白细胞介素-17 抑制剂引起的伴有内镜图像、内镜发现和病理特征的回结肠-结肠炎,包括本病例。其中 9 例表现为弥漫性血管模式丧失、左结肠粗厚的黏膜/溃疡形成,内镜表现类似于溃疡性结肠炎。其余 8 例则从末端回肠到直肠可见不连续的糜烂和溃疡,内镜表现类似于克罗恩病。在本病例中,胶囊内镜证实了这些发现,这在之前的报告中尚未报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b065/10494761/c708f1eeea61/WJG-29-4912-g001.jpg

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