医学
狼疮性肾炎
梅毒
膜性肾病
系统性红斑狼疮
肾活检
肾病
蛋白尿
抗核抗体
免疫学
肾病综合征
肾小球肾炎
胃肠病学
皮肤病科
内科学
病理
肾
自身抗体
抗体
内分泌学
疾病
糖尿病
人类免疫缺陷病毒(HIV)
作者
Moira Marie Scaperotti,Donghyang Kwon,Bhaskar Kallakury,Virginia Steen
出处
期刊:Case Reports
[BMJ]
日期:2021-08-01
卷期号:14 (8): e244466-e244466
被引量:6
标识
DOI:10.1136/bcr-2021-244466
摘要
We describe an unusual case of membranous nephropathy precipitated by syphilis infection in a patient without systemic lupus erythematosus (SLE). A previously healthy 20-year-old man presented with leg and facial swelling. Laboratory investigation revealed nephrotic range proteinuria, acute kidney injury, hypocomplementaemia and a highly positive rapid plasma reagin. Kidney biopsy showed membranous nephropathy with ‘full-house’ immunofluorescence (IgG, IgA, IgM, C1q and C3), mimicking lupus nephritis class Vb. However, the patient had no features of SLE and had negative antinuclear and anti-double-stranded DNA antibodies. He was treated with high-dose methylprednisolone and mycophenolate mofetil for lupus nephritis and with penicillin for syphilis. After 2 months of therapy, his proteinuria resolved, and his renal function and C4 level normalised. This case illustrates that syphilis infection can be a mimicker of lupus nephritis. A literature review suggests that ful-house nephropathy may occur independently of lupus nephritis and may or may not develop into SLE.
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