El Tawil Abdo I, Mendes Beatriz A, Machoski Leandro A F, Domingos Micheli F, Wassano Noelle S, Ioshii Sérgio O, Ramos Eduardo J B
Department of Research, Faculdade Evangélica Mackenzie do Paraná, Curitiba, PR, Brazil.
Department of Hepatobiliary Surgery, Hospital Nossa Senhora das Graças, Curitiba, PR, Brazil.
Am J Case Rep. 2025 Aug 28;26:e948580. doi: 10.12659/AJCR.948580.
BACKGROUND Immunotherapy has seen an exponential increase recently, as has the study of its associated adverse effects. Although a wide range of reactions to immunotherapy has been described, reports of immune-mediated focal pancreatitis remain rare. Autoimmune pancreatitis related to immune checkpoint inhibitors occurs because of the hyperactivation of T lymphocytes, which act against pancreatic cells, causing inflammation. CASE REPORT This case report describes a previously healthy 41-year-old man with a diagnosis of metastatic melanoma with inguinal lymph node metastasis. The patient underwent 1 year of adjuvant treatment with nivolumab and had excellent tolerance. After a 1-year suspension of this treatment, nodal and peritoneal recurrence occurred, leading to the initiation of combined therapy with ipilimumab and nivolumab, followed by maintenance nivolumab, resulting in a complete response. After 10 cycles of nivolumab, PET-CT and MRI identified a lesion in the head of the pancreas, which was suspected to be a primary neoplasm. The patient was asymptomatic, with normal tumor markers and elevated amylase and lipase levels. An endoscopic ultrasound-guided biopsy was performed to rule out primary pancreatic cancer, revealing moderately active chronic inflammation associated with immunotherapy. Nivolumab treatment was interrupted for 2 weeks, during which pancreatic enzyme levels improved. Treatment was resumed thereafter. The patient continued with monthly nivolumab applications, maintaining a complete response. without changes in imaging or laboratory test results. CONCLUSIONS This case is atypical for autoimmune pancreatitis owing to the absence of corticosteroid intervention, self-limiting nature of inflammation, and lack of inflammatory recurrence despite the continued use of immunotherapy.
背景 近年来免疫疗法呈指数级增长,其相关不良反应的研究亦是如此。尽管已描述了对免疫疗法的多种反应,但免疫介导的局灶性胰腺炎的报道仍然很少。与免疫检查点抑制剂相关的自身免疫性胰腺炎是由于T淋巴细胞过度活化,作用于胰腺细胞,引发炎症所致。病例报告 本病例报告描述了一名此前健康的41岁男性,诊断为伴有腹股沟淋巴结转移的转移性黑色素瘤。患者接受了1年的纳武单抗辅助治疗,耐受性良好。在该治疗中断1年后,出现淋巴结和腹膜复发,遂开始使用伊匹木单抗和纳武单抗联合治疗,随后进行纳武单抗维持治疗,结果达到完全缓解。在接受10个周期的纳武单抗治疗后,PET-CT和MRI在胰头发现一个病灶,怀疑是原发性肿瘤。患者无症状,肿瘤标志物正常,淀粉酶和脂肪酶水平升高。进行了内镜超声引导下活检以排除原发性胰腺癌,结果显示为与免疫疗法相关的中度活动性慢性炎症。纳武单抗治疗中断2周,在此期间胰腺酶水平有所改善。此后恢复治疗。患者继续每月应用纳武单抗,维持完全缓解状态,影像学和实验室检查结果均无变化。结论 该病例对于自身免疫性胰腺炎而言不典型,原因在于未进行皮质类固醇干预、炎症具有自限性且尽管继续使用免疫疗法但未出现炎症复发。