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免疫检查点抑制剂相关的乳糜泻病例报告。

A case of checkpoint inhibitor-induced celiac disease.

机构信息

Department of Internal Medicine, MedStar Georgetown University Hospital, Washington, DC, USA.

Lombardi Comprehensive Cancer Center, MedStar Georgetown University Hospital, 3800 Reservoir Road, NW, Washington, DC, 20007, USA.

出版信息

J Immunother Cancer. 2019 Aug 5;7(1):203. doi: 10.1186/s40425-019-0694-x.

Abstract

BACKGROUND

Immune checkpoint inhibitors (ICIs) have now become standard of care treatment for many malignancies. ICIs are associated with unique immune mediated adverse events (irAEs) due to dysregulation of immune activation. As treatment with ICIs is becoming more common, rare irAEs are also being recognized. Here we report a case of ICI-induced celiac disease.

CASE

A 74-year-old Caucasian female with metastatic renal carcinoma received second line nivolumab (anti-PD1 antibody) after initial disease progression on sunitinib. Ipilimumab was added after she failed to respond to six cycles of nivolumab monotherapy. One week after her first cycle of combination treatment, she presented with nausea, vomiting, grade 1 diarrhea, and weight loss. She underwent endoscopy, which showed bile stasis in the stomach, normal appearing stomach mucosa, and nonbleeding erythematous mucosa in the duodenal bulb. Stomach biopsy showed moderate active chronic gastritis. Duodenal biopsy showed moderate chronic active duodenitis with focal neutrophilic cryptitis, mucosal erosions, villous atrophy, mildly increased intraepithelial lymphocytes, and moderate chronic inflammation in the lamina propria pathognomonic of celiac disease. Symptoms improved with gluten-free diet, twice-daily omeprazole and anti-emetics and she was able to continue on treatment.

CONCLUSIONS

There has been only one published case reporting ICI-induced celiac disease. Our case report highlights a rare irAE (celiac disease) associated with ICI treatment. It is unclear whether the patient had previously undiagnosed celiac disease or whether ICIs triggered her enteritis. Our patient was able to continue treatment with ICIs with dietary modifications, suggesting correct diagnosis is critical for optimal patient outcome.

摘要

背景

免疫检查点抑制剂(ICI)现已成为许多恶性肿瘤的标准治疗方法。由于免疫激活失调,ICI 与独特的免疫介导的不良反应(irAE)相关。随着 ICI 的治疗越来越普遍,也认识到了罕见的 irAE。本文报告了一例 ICI 诱导的乳糜泻。

病例

一名 74 岁白人女性,转移性肾细胞癌,在舒尼替尼初始疾病进展后接受二线纳武单抗(抗 PD-1 抗体)治疗。在她对纳武单抗单药治疗的六周期无反应后,加用伊匹单抗。在联合治疗的第一周期后一周,她出现恶心、呕吐、1 级腹泻和体重减轻。她接受了内镜检查,显示胃中有胆汁淤积,胃黏膜正常,十二指肠球部有非出血性红斑状黏膜。胃活检显示中度活动性慢性胃炎。十二指肠活检显示中度慢性活动性十二指肠炎,伴有局灶性中性粒细胞隐窝炎、黏膜糜烂、绒毛萎缩、上皮内淋巴细胞轻度增加和固有层中度慢性炎症,这些特征符合乳糜泻。通过无麸质饮食、每日两次奥美拉唑和止吐药治疗后症状得到改善,她能够继续接受治疗。

结论

仅有一例发表的病例报告了 ICI 诱导的乳糜泻。我们的病例报告强调了与 ICI 治疗相关的罕见 irAE(乳糜泻)。尚不清楚患者是否以前患有未确诊的乳糜泻,还是 ICI 引发了她的肠炎。我们的患者通过饮食调整能够继续接受 ICI 治疗,这表明正确的诊断对于患者的最佳治疗效果至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1b0/6683380/7fcccd5b3e36/40425_2019_694_Fig1_HTML.jpg

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