Fadel Ahmed R, Mayank Vipul, Lohani Sudhir
Respiratory Medicine, Dartford and Gravesham NHS Trust, Dartford, GBR.
General Medicine, Dartford and Gravesham NHS Trust, Dartford, GBR.
Cureus. 2025 Jul 9;17(7):e87618. doi: 10.7759/cureus.87618. eCollection 2025 Jul.
Granulomatosis with polyangiitis (GPA) is an anti-neutrophil cytoplasmic antibodies (ANCA)-associated vasculitis that typically affects the upper and lower respiratory tract and kidneys. Cardiac complications, particularly those involving the valvular or subvalvular structures, are rare. We present the case of a 59-year-old woman with known anti-proteinase 3 (PR3)-ANCA-positive GPA who developed a severe disease flare characterized by diffuse alveolar hemorrhage (DAH) and mitral valve insufficiency due to chordae tendineae rupture. The diagnosis was confirmed by high-resolution computed tomography demonstrating ground-glass opacities consistent with DAH, markedly elevated PR3-ANCA titers, and echocardiography showing severe mitral regurgitation with ruptured chordae. She was treated with high-dose corticosteroids, rituximab, and avacopan, which resulted in marked clinical and radiological improvements. This case highlights the need for increased awareness of rare GPA manifestations, importance of multidisciplinary evaluation, and potential benefits of early immunosuppressive therapy.
肉芽肿性多血管炎(GPA)是一种抗中性粒细胞胞浆抗体(ANCA)相关性血管炎,通常累及上、下呼吸道及肾脏。心脏并发症,尤其是累及瓣膜或瓣膜下结构的并发症较为罕见。我们报告一例59岁女性,已知抗蛋白酶3(PR3)-ANCA阳性GPA,因腱索断裂出现以弥漫性肺泡出血(DAH)和二尖瓣关闭不全为特征的严重疾病发作。高分辨率计算机断层扫描显示与DAH一致的磨玻璃影、PR3-ANCA滴度显著升高以及超声心动图显示伴有腱索断裂的严重二尖瓣反流,确诊了该病例。她接受了大剂量糖皮质激素、利妥昔单抗和阿伐可泮治疗,临床和影像学均有明显改善。该病例强调了提高对罕见GPA表现的认识、多学科评估的重要性以及早期免疫抑制治疗的潜在益处。