自身免疫性胰腺炎患者的白细胞碎裂性和肾血管炎：新的关联。
Leucocytoclastic and renal vasculitis in a patient with autoimmune pancreatitis: new associations.
机构信息
Department of Gastroenterology, St Vincent's Hospital Melbourne, Melbourne, Victoria, Australia.
出版信息
Intern Med J. 2010 May;40(5):376-80. doi: 10.1111/j.1445-5994.2010.02175.x.
Autoimmune pancreatitis (AIP) is an uncommon condition which comprises diffuse or discrete pancreatic enlargement and irregular pancreatic duct strictures of autoimmune origin leading to pain or obstructive jaundice associated with extra-pancreatic manifestations. It is characterized by an elevated IgG, especially IgG4, level. We illustrate the first described case of a patient with AIP in association with leucocytoclastic and renal vasculitis.
自身免疫性胰腺炎（AIP）是一种罕见的疾病，其特征为弥漫性或局灶性胰腺肿大和不典型的胰管狭窄，这些狭窄由自身免疫引起，导致疼痛或阻塞性黄疸，并伴有胰腺外表现。该病的特征为 IgG 水平升高，尤其是 IgG4。我们首次描述了一例 AIP 患者合并白细胞碎裂性血管炎和肾血管炎的病例。
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