Beniada Camille, Coattrenec Yann, Mack Sahar, Ricoeur Alexis, Adsay Volkan, Puppa Giacomo, Seebach Jörg D
Division of Immunology and Allergy, Department of Medicine, University Hospitals of Geneva, Geneva, Switzerland.
Division of Gastroenterology and Hepatology, Department of Medicine, University Hospitals of Geneva, Geneva, Switzerland.
Am J Case Rep. 2025 May 31;26:e945741. doi: 10.12659/AJCR.945741.
BACKGROUND The spectrum of anti-neutrophil cytoplasmic antibodies (ANCA)-associated vasculitis (AAV) encompasses granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis (EGPA). These pathologies predominantly affect small to medium-sized vessels, with frequent involvement of the ear, nose, and throat (ENT) sphere, lungs, and kidneys. Pancreatic involvement, an exceedingly rare manifestation of AAV, manifests as pancreatitis, a pancreatic mass, or a cystic lesion. This study reports a new case of pancreatic GPA and reviews the literature to characterize its clinical, radiological, and histological features. CASE REPORT A 54-year-old woman with severe epigastric pain, vomiting, and weight loss presented with a pancreatic mass and peripancreatic lymphadenitis on imaging studies, raising high suspicion for cancer. Repeated endoscopic ultrasound-guided fine-needle aspiration (EUS-FNA) biopsies were inconclusive. Distal pancreatectomy with splenectomy was performed. Histopathology demonstrated granulomatous inflammation with necrosis and vasculitis, and anti-PR3 ANCA testing was positive. A diagnosis of GPA was made and treatment with corticosteroids and rituximab resulted in clinical remission. We identified 54 additional cases of pancreatic AAV in the literature and analyzed their clinical features. CONCLUSIONS In cases of unexplained pancreatitis or pancreatic masses/pseudocysts, AAV should be considered. A targeted evaluation - including ANCA testing, imaging, biopsies, and a systematic search for ENT, lung, kidney, and skin manifestations - is essential to identify key clinical, serological, and radiological clues of pancreatic AAV. We propose to classify this as type 4 autoimmune pancreatitis. A corticosteroid-based regimen, with or without additional immunosuppressants, offers effective disease control, making pancreatic surgery unnecessary.
背景 抗中性粒细胞胞浆抗体(ANCA)相关血管炎(AAV)谱系包括肉芽肿性多血管炎(GPA)、显微镜下多血管炎(MPA)和嗜酸性肉芽肿性多血管炎(EGPA)。这些病变主要累及中小血管,常累及耳、鼻、喉(ENT)、肺和肾脏。胰腺受累是AAV极为罕见的表现,表现为胰腺炎、胰腺肿块或囊性病变。本研究报告了一例胰腺GPA新病例,并回顾文献以描述其临床、放射学和组织学特征。病例报告 一名54岁女性,有严重上腹痛、呕吐和体重减轻,影像学检查显示胰腺肿块和胰腺周围淋巴结炎,高度怀疑为癌症。反复内镜超声引导下细针穿刺(EUS-FNA)活检结果不明确。行远端胰腺切除术加脾切除术。组织病理学显示肉芽肿性炎症伴坏死和血管炎,抗PR3 ANCA检测呈阳性。诊断为GPA,使用皮质类固醇和利妥昔单抗治疗后临床缓解。我们在文献中又确定了54例胰腺AAV病例,并分析了它们的临床特征。结论 在不明原因的胰腺炎或胰腺肿块/假性囊肿病例中,应考虑AAV。进行有针对性的评估——包括ANCA检测、影像学检查、活检以及系统寻找ENT、肺、肾和皮肤表现——对于识别胰腺AAV的关键临床、血清学和放射学线索至关重要。我们建议将其归类为4型自身免疫性胰腺炎。基于皮质类固醇的治疗方案,无论是否加用其他免疫抑制剂,都能有效控制疾病,无需进行胰腺手术。