Department of Internal Medicine, University Hospital of Nantes, France.
Department of Pathology, University Hospital of Nantes, France.
Cardiovasc Pathol. 2014 Nov-Dec;23(6):363-5. doi: 10.1016/j.carpath.2014.07.007. Epub 2014 Aug 4.
Granulomatosis with polyangiitis (GPA) (Wegener's) is a necrotizing systemic vasculitis of the small-sized blood vessels, affecting kidneys, lungs, upper respiratory tract and skin. Cardiac valvular involvement is an uncommon manifestation of GPA. We report the case of a 60-year-old woman with arthritis and lung nodules due to GPA without antineutrophil cytoplasmic antibodies (ANCA) at time of diagnosis. Remission was obtained with cyclophosphamide and corticosteroid. Azathioprine was then prescribed for 2years. Four years later, she developed severe inflammatory aortic and mitral valvular involvement characterized by GPA typical histopathological valvular lesions. Search for ANCA was positive at this time (anti-myeloperoxidase). Cardiac valvular involvement is a rare and potentially fatal complication of GPA and may misleadingly suggest infectious endocarditis. A review of literature revealed few cases of histologically well-documented cardiac valvular involvement in GPA. Pathologists should be aware of valvular heart diseases in GPA, which usually comprise valvular necrotic lesions without any microbial agents.
肉芽肿性多血管炎(GPA)(韦格纳氏)是一种小血管坏死性系统性血管炎,影响肾脏、肺部、上呼吸道和皮肤。心脏瓣膜受累是 GPA 的一种不常见表现。我们报告了一例 60 岁女性因 GPA 出现关节炎和肺部结节,但在诊断时无抗中性粒细胞胞浆抗体(ANCA)。用环磷酰胺和皮质类固醇治疗后缓解。随后,给予她 2 年的硫唑嘌呤治疗。4 年后,她出现严重的炎症性主动脉瓣和二尖瓣受累,其特征是 GPA 典型的组织病理学瓣膜病变。此时 ANCA 检测呈阳性(抗髓过氧化物酶)。心脏瓣膜受累是 GPA 的一种罕见且潜在致命的并发症,可能会误导性地提示感染性心内膜炎。文献复习显示,GPA 中有少数经组织学明确诊断的心脏瓣膜受累病例。病理学家应注意 GPA 中的瓣膜性心脏病,其通常包含无任何微生物因素的瓣膜坏死性病变。