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Severe Luminal Stricture in Immune-related Adverse Event-associated Enteritis, a Case Report Akifumi Fukui 1 , Yusuke Okuyama 1 , Go Sawai 1 , Makoto Tanaka 1 , Yutaka Inada 1 , Yoshikazu Nakatsugawa 1 , Naoya Tomatsuri 1 , Jun Ikeda 2 , Hideki Sato 1 , Yoji Urata 3 1Department of Gastroenterology and Hepatology, Japanese Red Cross Society Kyoto Daiichi Hospital, Kyoto, Japan 2Department of Gastroenterological Surgery, Japanese Red Cross Society Kyoto Daiichi Hospital, Kyoto, Japan 3Department of Pathology, Japanese Red Cross Society Kyoto Daiichi Hospital, Kyoto, Japan Keyword: 免疫チェックポイント阻害薬 , 免疫関連有害事象 , 小腸炎 , 大腸炎 , 管腔狭窄 pp.1713-1719
Published Date 2025/12/25
DOI https://doi.org/10.11477/mf.053621800600121713
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 Immune checkpoint inhibitors, including ipilimumab and nivolumab, target cytotoxic T-lymphocyte-associated antigen 4 and programmed cell death protein 1, respectively, and are increasingly used in cancer treatment. These therapies can induce immune-related adverse events, including colitis and ileitis. However, reports on enteritis caused by these immune-related adverse events are lacking, particularly in Japan, with only a few case reports available. The incidence, typical location, and timing of onset of such inflammation remain undefined. We present the case of a 56-year-old man who developed severe colitis and enteritis after receiving immune checkpoint inhibitor therapy for a recurrent metastatic lung tumor following surgical treatment for renal cell carcinoma. Despite administration of high-dose prednisolone and infliximab, he developed colonic perforation, requiring subtotal proctocolectomy and colostomy. At 6 months postoperatively, he presented with enteritis with luminal narrowing. Oral budesonide was initiated, and endoscopic balloon dilation of the stenotic site improved the obstruction. Consequently, 3.5 years after initiating immune checkpoint inhibitor therapy, no recurrence of the metastatic lung tumor was noted and the patient is alive without any difficulties in oral intake. This report highlights the need for careful consideration of immune checkpoint inhibitor administration, even during transitions to a single-agent therapy.


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電子版ISSN 1882-1219 印刷版ISSN 0536-2180 医学書院

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