Lupus Podocytopathy: A Rare Cause of Nephrotic Syndrome in Patients with Systemic Lupus Erythematosus.
Lupus nephritis
Lupus podocytopathy
Minimal change disease
Nephrotic syndrome
SLE
Journal
Journal of community hospital internal medicine perspectives
ISSN: 2000-9666
Titre abrégé: J Community Hosp Intern Med Perspect
Pays: United States
ID NLM: 101601396
Informations de publication
Date de publication:
2023
2023
Historique:
received:
24
02
2023
revised:
30
04
2023
accepted:
15
05
2023
medline:
23
10
2023
pubmed:
23
10
2023
entrez:
23
10
2023
Statut:
epublish
Résumé
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 podocytopathy 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.
Identifiants
pubmed: 37868666
doi: 10.55729/2000-9666.1218
pii: jchim-13-05-057
pmc: PMC10589041
doi:
Types de publication
Case Reports
Langues
eng
Pagination
57-60Informations de copyright
© 2023 Greater Baltimore Medical Center.
Déclaration de conflit d'intérêts
Conflict of interest There is no conflict of interest.
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