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Updated: Jul 11, 2026

Analyses of Proteinuria, Renal Infiltration of Leukocytes, and Renal Deposition of Proteins in Lupus-prone MRL/lpr Mice
Published on: June 8, 2022
Pauci-immune glomerulonephritis associated with primary antiphospholipid syndrome
Fatih Dede1, Yasin Simsek, Ali Riza Odabas
1Department of Nephrology, Ankara Numune Training and Research Hospital, Samanpazari/Ankara 06100, Turkey. fatded@yahoo.com
Abstract:
The antiphospholipid syndrome (APS) is characterized by thrombotic events associated with the presence of antiphospholipid antibodies. Renal involvement is a frequent feature in patients with APS. APS presenting with proteinuria showed that the renal involvement in this syndrome could also be a different form of glomerulonephritis. We describe a rare case report of pauci-immune vasculitis associated with primary APS in the absence of other underlying autoimmune disorders.
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