Speer Claudius, Gaida Matthias Martin, Waldherr Rüdiger, Nusshag Christian, Kälble Florian, Zeier Martin
Department of Nephrology, Heidelberg University Hospital, Heidelberg, Germany.
Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany.
SAGE Open Med Case Rep. 2018 Oct 19;6:2050313X18807621. doi: 10.1177/2050313X18807621. eCollection 2018.
Membranous nephropathy is a common cause of nephrotic syndrome in adults and can be primary or secondary through autoimmune disease, medication, infection, or malignancy. Rapidly progressive glomerulonephritis with crescent formation is rare in patients with membranous nephropathy. Thus, in cases with rapid decline in renal function, after excluding complications such as malignant hypertension, acute hypersensitivity interstitial nephritis, and bilateral renal vein thrombosis, the simultaneous occurrence of a superimposed glomerulonephritis should be considered. We report a 55-year-old man suffering from a biopsy-confirmed primary membranous nephropathy, who developed rapidly progressive glomerulonephritis with anti-glomerular basement membrane antibodies after being affected with membranous nephropathy for 8 years. The kidney biopsy revealed a concurrence of membranous nephropathy and anti-glomerular basement membrane disease. Clinical presentation and treatment of membranous nephropathy followed by anti-glomerular basement membrane disease are discussed based on our observation with promising follow-up.
膜性肾病是成人肾病综合征的常见病因,可原发或继发于自身免疫性疾病、药物、感染或恶性肿瘤。膜性肾病患者中出现伴有新月体形成的快速进展性肾小球肾炎较为罕见。因此,在肾功能迅速下降的病例中,排除恶性高血压、急性过敏性间质性肾炎和双侧肾静脉血栓形成等并发症后,应考虑同时合并有叠加性肾小球肾炎。我们报告一例55岁男性,经活检确诊为原发性膜性肾病,在患膜性肾病8年后出现伴有抗肾小球基底膜抗体的快速进展性肾小球肾炎。肾脏活检显示膜性肾病与抗肾小球基底膜病并存。基于我们的观察及有前景的随访结果,对膜性肾病后继发抗肾小球基底膜病的临床表现及治疗进行了讨论。