Granulomatosis with Polyangiitis Presenting as Pancreatic Pseudotumor and Peripancreatic Lymphadenitis: Diagnostic Challenges and Review of 55 Cases.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Camille Beniada, Yann Coattrenec, Sahar Mack, Alexis Ricoeur, Volkan Adsay, Giacomo Puppa, Jörg D Seebach
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引用次数: 0

Abstract

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.

肉芽肿病合并多血管炎表现为胰腺假瘤和胰周淋巴结炎:诊断挑战和55例回顾。
抗中性粒细胞胞浆抗体(ANCA)相关血管炎(AAV)的谱包括肉芽肿病合并多血管炎(GPA)、显微多血管炎(MPA)和嗜酸性肉芽肿病合并多血管炎(EGPA)。这些病变主要影响中小血管,常累及耳、鼻、喉(耳鼻喉)球体、肺和肾。累及胰腺是AAV极为罕见的表现,表现为胰腺炎、胰腺肿块或囊性病变。本研究报告一例新的胰腺GPA病例,并回顾文献以描述其临床、影像学和组织学特征。病例报告:一名54岁女性,严重胃脘痛、呕吐和体重减轻,影像学检查显示胰腺肿块和胰周淋巴结炎,高度怀疑为癌症。反复内镜超声引导下细针穿刺活检(EUS-FNA)尚无定论。行远端胰切除术并脾切除术。组织病理学表现为肉芽肿性炎症伴坏死和血管炎,抗pr3 ANCA检测阳性。诊断为GPA,用皮质类固醇和利妥昔单抗治疗导致临床缓解。我们在文献中发现了54例胰腺AAV病例,并分析了他们的临床特征。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。有针对性的评估——包括ANCA检测、成像、活检,以及系统地搜索耳鼻喉科、肺、肾和皮肤表现——对于确定胰腺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。以皮质类固醇为基础的治疗方案,有或没有额外的免疫抑制剂,提供有效的疾病控制,使胰腺手术不必要。
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来源期刊
American Journal of Case Reports
American Journal of Case Reports Medicine-Medicine (all)
CiteScore
1.80
自引率
0.00%
发文量
599
期刊介绍: American Journal of Case Reports is an international, peer-reviewed scientific journal that publishes single and series case reports in all medical fields. American Journal of Case Reports is issued on a continuous basis as a primary electronic journal. Print copies of a single article or a set of articles can be ordered on demand.
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