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以胰腺肿块为首发表现的结节性多动脉炎:1例病例报告并文献复习

Pancreatic mass as an initial manifestation of polyarteritis nodosa: a case report and review of the literature.

作者信息

Yokoi Yoshihiro, Nakamura Ippei, Kaneko Takeshi, Sawayanagi Tomoki, Watahiki Youichi, Kuroda Makoto

机构信息

Yoshihiro Yokoi, Takeshi Kaneko, Tomoki Sawayanagi, Youichi Watahiki, Department of Surgery, Shinshiro Municipal Hospital, Aichi 441-1387, Japan.

出版信息

World J Gastroenterol. 2015 Jan 21;21(3):1014-9. doi: 10.3748/wjg.v21.i3.1014.

Abstract

Classic polyarteritis nodosa (PAN) that targets medium-sized muscular arteries and microscopic polyangiitis (MPA), characterized by inflammation of small-caliber vessels and the presence of circulating myeloperoxidase anti-neutrophil cytoplasmic antibodies (MPO-ANCA), are distinct clinicopathological entities of systemic vasculitis. A 66-year-old woman presented with fever, cholestasis and positive MPO-ANCA. Radiological examination showed a pancreatic mass compressing the bile duct. Therefore, we performed pancreatoduodenectomy. Histopathological examination revealed that necrotizing vasculitis predominantly affecting the medium-sized vessels, spared arterioles or capillaries in the pancreas, a finding consistent with PAN. Unexpectedly, renal biopsy revealed small-caliber vasculitis and glomerulonephritis, supporting MPA. The initial manifestation of a pancreatic mass associated with vasculitis has only been reported in 7 articles. Its diagnosis is challenging because no reliable clinico-radiological findings have been observed. Clinicians should be aware of such cases and early diagnosis followed by immunosuppression is mandatory. Our findings may reflect a polyangiitis overlap syndrome coexisting between pancreatic PAN and renal MPA.

摘要

经典结节性多动脉炎(PAN)累及中等大小肌性动脉,显微镜下多血管炎(MPA)以小口径血管炎症及循环髓过氧化物酶抗中性粒细胞胞浆抗体(MPO-ANCA)阳性为特征,它们是系统性血管炎不同的临床病理实体。一名66岁女性出现发热、胆汁淤积及MPO-ANCA阳性。影像学检查显示胰腺肿物压迫胆管。因此,我们实施了胰十二指肠切除术。组织病理学检查显示坏死性血管炎主要累及中等大小血管,胰腺小动脉或毛细血管未受累,这一发现符合PAN。出乎意料的是,肾活检显示小口径血管炎和肾小球肾炎,支持MPA诊断。仅7篇文献报道过胰腺肿物合并血管炎的初始表现。由于未观察到可靠的临床影像学表现,其诊断具有挑战性。临床医生应意识到此类病例,早期诊断并给予免疫抑制治疗是必要的。我们的发现可能反映了胰腺PAN和肾MPA之间共存的多血管炎重叠综合征。

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