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膜性肾病与抗中性粒细胞胞浆抗体相关性血管炎的伴发组织学特征

Concomitant Histological Features of Membranous Nephropathy and Anti-Neutrophil Cytoplasmic Antibody Associated Vasculitis.

作者信息

Rajesh Chilaka, Mishra Utkarash, Roy Sanjeet, Alam Rizwan, Mani Selvin Sundar Raj, Eapen Jeethu Joseph, Thomas Athul, Alexander Suceena, Varughese Santosh, David Vinoi George

机构信息

Department of Nephrology, Christian Medical College, Vellore, Tamil Nadu, India.

Department of Pathology, Christian Medical College, Vellore, Tamil Nadu, India.

出版信息

Indian J Nephrol. 2025 Jan-Feb;35(1):105-108. doi: 10.25259/IJN_140_2024. Epub 2024 Jul 15.

Abstract

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.

摘要

血管炎性肾小球肾炎和膜性肾病同时出现的情况并不常见。我们报告了两例因快速进展性肾衰竭前来我院门诊就诊的病例。经评估,其中一名患者抗髓过氧化物酶(MPO)滴度较高,肾活检提示同时存在坏死性和弥漫性新月体性抗MPO抗中性粒细胞胞浆抗原相关性肾小球肾炎,伴有环周性细胞新月体形成及膜性肾小球病。他接受了血浆置换治疗,随后口服环磷酰胺进行维持性免疫抑制治疗。另一名患者接受了甲泼尼龙和两剂利妥昔单抗治疗。两名患者均表现出明显的症状改善,3个月时肌酐稳定,无需透析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ac/11763016/07f7994aa114/IJN-35-1-105-g1.jpg

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