Lupus Podocytopathy: A Rare Cause of Nephrotic Syndrome in Patients with Systemic Lupus Erythematosus

被引：0

作者：

Khan, Omair ^{[1
]}

Mohammadrezaei, Fatemeh ^{[1
]}

Aslam, Sadia ^{[1
]}

Khan, Mohammad H. ^{[2
]}

Wilches, Rita D. M. ^{[1
]}

Singh, Sehajpreet ^{[1
]}

Scheers-Masters, Joshua ^{[1
]}

机构：

[1] Maimonides Hosp, Brooklyn, NY USA

[2] Shifa Coll Med, Islamabad, Pakistan

来源：

JOURNAL OF COMMUNITY HOSPITAL INTERNAL MEDICINE PERSPECTIVES | 2023年 / 13卷 / 05期

关键词：

Lupus podocytopathy; Nephrotic syndrome; SLE; Lupus nephritis; Minimal change disease; NEPHRITIS; THERAPY;

D O I：

10.55729/2000-9666.1218

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Lupus podocytopathy, a unique form of lupus nephritis, mimics minimal change disease (MCD) or primary focal segmental glomerulosclerosis (FSGS) and represents approximately 1% of lupus nephritis biopsies. Lupus podocytop-athy is characterized by diffuse epithelial cell foot process effacement without immune complex deposition or with only mesangial immune complex deposition. We present the case of a young woman with systemic lupus erythematosus (SLE) who presented with nephrotic syndrome and acute kidney injury (AKI) and was subsequently diagnosed with lupus podocytopathy.

引用

页码：57 / 60

页数：6

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