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Occult systemic lupus erythematosus with active lupus nephritis presenting as Libman-Sacks endocarditis

机译:隐匿性系统性红斑狼疮伴活动性狼疮肾炎,表现为利比曼-萨克斯心内膜炎

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摘要

The diagnosis of systemic lupus erythematosus (SLE) depends on clinical evidence of renal, rheumatologic, cutaneous, and neurologic involvement, supported by serological markers. A previously healthy 14-year-old girl presented with Libman-Sacks endocarditis involving the aortic valve as the first manifestation of SLE. Even though she did not satisfy the American College of Rheumatology criteria for diagnosing SLE, she had anemia, proteinuria, elevated erythrocyte sedimentation rate, low complement 4 (C4) levels, and strongly positive antinuclear antibody titer. A renal biopsy showed stage IV lupus nephritis. Treatment was initiated with immunosuppressants and steroids. This type of presentation may be misdiagnosed as infective endocarditis missing the underlying collagen vascular disease.
机译:系统性红斑狼疮(SLE)的诊断取决于在血清学指标支持下的肾脏,风湿病,皮肤和神经系统受累的临床证据。先前健康的14岁女孩出现了以主动脉瓣为主要症状的Libman-Sacks心内膜炎。尽管她不符合美国风湿病学会诊断SLE的标准,但仍患有贫血,蛋白尿,红细胞沉降率升高,补体4(C4)水平低以及抗核抗体滴度很强。肾活检显示IV期狼疮性肾炎。用免疫抑制剂和类固醇开始治疗。这类表现可能被误诊为感染性心内膜炎,缺少潜在的胶原蛋白血管疾病。

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