Uijtterhaegen Gilles, De Donder Laura, Ameloot Eline, Lefebvre Kristof, Van Dorpe Jo, De Pauw Michel, François Katrien
Department of Cardiac Surgery, Ghent University Hospital, Corneel Heymanlaan 10, 9000 Ghent, Belgium.
Department of Pathology, Ghent University Hospital, Ghent, Corneel Heymanlaan 10, 9000 Ghent, Belgium.
Eur Heart J Case Rep. 2020 Oct 6;4(5):1-6. doi: 10.1093/ehjcr/ytaa307. eCollection 2020 Oct.
Granulomatosis with polyangiitis (GPA), formerly known as Wegener's granulomatosis, is a systemic inflammatory process predominantly affecting upper and lower respiratory tract and kidneys. Valvular heart disease is a rare manifestation of GPA.
We report two cases of acute valvular heart disease mimicking acute endocarditis caused by GPA. Both patients were middle-aged females with acute aortic valve regurgitation suggestive of possible infective endocarditis. In their recent medical history, atypical otitis and sinusitis were noted. The first patient was admitted with heart failure and the second patient because of persisting fever. Echocardiogram revealed severe aortic regurgitation with an additional structure on two cusps, suggestive of infective endocarditis in both patients. Urgent surgical replacement was performed; however, intraoperative findings did not show infective endocarditis, but severe inflammatory changes of the valve and surrounding tissue. In both patients, the valve was replaced by a prosthetic valve. Microscopic examination of the valve/myocardial biopsy showed diffuse acute and chronic inflammation with necrosis and necrotizing granulomas, compatible with GPA after infectious causes were excluded. Disease remission was obtained in both patients, in one patient with Rituximab and in the other with Glucocorticoids and Cyclophosphamide. Both had an uneventful follow-up.
Granulomatosis with polyangiitis can be a rare cause of acute aortic valve regurgitation mimicking infective endocarditis with the need for surgical valve replacement. Atypical ear, nose, and throat symptoms can be a first sign of GPA. Symptom recognition is important for early diagnosis and appropriate treatment to prevent further progression of the disease.
肉芽肿性多血管炎(GPA),既往称为韦格纳肉芽肿,是一种主要影响上、下呼吸道及肾脏的全身性炎症过程。瓣膜性心脏病是GPA的一种罕见表现。
我们报告两例由GPA引起的酷似急性感染性心内膜炎的急性瓣膜性心脏病病例。两名患者均为中年女性,均有提示可能为感染性心内膜炎的急性主动脉瓣反流。在她们近期的病史中,均有非典型中耳炎和鼻窦炎。第一名患者因心力衰竭入院,第二名患者因持续发热入院。超声心动图显示严重主动脉反流,两个瓣叶上有额外结构,提示两名患者均有感染性心内膜炎。均进行了紧急手术置换;然而,术中发现未显示感染性心内膜炎,而是瓣膜及周围组织有严重炎症改变。两名患者均用人工瓣膜置换了瓣膜。对瓣膜/心肌活检的显微镜检查显示弥漫性急性和慢性炎症伴坏死及坏死性肉芽肿,在排除感染性病因后符合GPA。两名患者均病情缓解,一名患者用利妥昔单抗治疗,另一名患者用糖皮质激素和环磷酰胺治疗。两人随访均顺利。
肉芽肿性多血管炎可能是酷似感染性心内膜炎并需要进行手术瓣膜置换的急性主动脉瓣反流的罕见病因。非典型的耳、鼻、喉症状可能是GPA的首发症状。症状识别对于早期诊断和恰当治疗以防止疾病进一步进展很重要。