IMR Press / CEOG / Volume 33 / Issue 2 / pii/2006033

Clinical and Experimental Obstetrics & Gynecology (CEOG) is published by IMR Press from Volume 47 Issue 1 (2020). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with S.O.G.

Case Report

A rare case of early onset nephrotic syndrome in pregnancy

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1 Department of Obstetrics and Gynecology, Marmara University School of Medicine, Istanbul (Turkey)
2 Department of Pathology, Marmara University School of Medicine, Istanbul (Turkey)
3 Department of Anesthesiology, Sisli Etfal Training and Education Hospital, Istanbul (Turkey)
Clin. Exp. Obstet. Gynecol. 2006, 33(2), 127–128;
Published: 10 June 2006
Abstract

Nephrotic syndrome occurs very rarely, about 0.012-0.025% of all pregnancies. Here, we report a rare case of early onset nephrotic syndrome developing de novo in the l7th week of pregnancy. A renal biopsy was done and the specimens revealed typical features of focal segmental glomerulosclerosis. The patient had a progressive clinical course of disease despite steroid treatment. Suffering from severe intrauterine growth restriction, the fetus died in utero. After delivery, steroid treatment was continued. The patient had normal renal function with a decrease in proteinuria in the second and fifth month postpartum. This report points out the poor fetal prognosis associated with an early onset nephrotic syndrome. Pregnant patients with early onset nephrotic syndrome should be carefully evaluated for the presence of chronic renal disease, and primary renal pathology should be included in the differential diagnosis of massive proteinuria in early pregnancy.

Keywords
Nephrotic syndrome
Pregnancy
Fetal outcome
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