膜性肾病和抗中性粒细胞胞浆抗体相关性血管炎的共同组织学特征

Pub Date : 2024-07-15 DOI:10.25259/ijn_140_2024
C. Rajesh, Utkarash Mishra, Sanjeet Roy, R. Alam, S. Mani, J. Eapen, Athul Thomas, S. Alexander, S. Varughese, V. David
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引用次数: 0

摘要

同时出现血管性肾小球肾炎和膜性肾病的情况并不多见。我们报告了两例因快速进展性肾衰竭而到我院门诊就诊的病例。经评估,其中一名患者的抗髓过氧化物酶(MPO)滴度较高,肾活检提示同时存在坏死性和弥漫性新月体抗MPO抗中性粒细胞胞浆抗原相关性肾小球肾炎,并伴有周缘细胞新月体形成和膜性肾小球病变。他对血浆置换术反应良好,随后口服环磷酰胺维持免疫抑制。另一名患者接受了甲泼尼龙和两剂利妥昔单抗治疗。这两名患者的症状都得到了明显改善,3 个月后肌酐稳定,不再需要透析。
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Concomitant Histological Features of Membranous Nephropathy and Anti-Neutrophil Cytoplasmic Antibody Associated Vasculitis
The simultaneous occurrence of vasculitic glomerulonephritis and membranous nephropathy is unusual. We report two cases that presented to our outpatient department with rapidly progressive renal failure. On evaluation, in one patient, anti-myeloperoxidase (MPO) titers were high, and renal biopsy was suggestive of concurrent necrotizing and diffuse crescentic anti-MPO anti-neutrophil cytoplasmic antigen-associated glomerulonephritis with the circumferential cellular crescent formation and membranous glomerulopathy. He responded to plasmapheresis followed by maintenance immunosuppression with oral cyclophosphomide. Another patient was treated with Methylprednisolone and two doses of rituximab. Both the patients showed marked symptomatic improvement and became dialysis independent with stable creatinine at 3 months.
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