Podocytopathy Associated with IgA Nephropathy in Pregnancy: A Challenging Association

Author:

Orozco Guillén Alejandra1ORCID,Soto Abraham Virgilia2,Moguel Gonzalez Bernardo3,Piccoli Giorgina4ORCID,Madero Magdalena3

Affiliation:

1. Nephrology Department, Instituto Nacional de Perinatología “Isidro Espinosa de los Reyes”, Mexico City 11000, Mexico

2. Department of Pathology, Ignacio Chávez National Institute of Cardiology, Mexico City 14080, Mexico

3. Department of Nephrology, Ignacio Chávez National Institute of Cardiology, Mexico City 14080, Mexico

4. Nephrologie, Department of Medicine, Centre Hospitalier Le Mans, 72037 Le Mans, France

Abstract

IgA nephropathy is the most common form of primary glomerulonephritis. While associations of IgA and other glomerular diseases have been described, the association of IgA nephropathy with “primary” podocytopathy is rare and has not been reported in pregnancy, due in part to the infrequent use of kidney biopsy during pregnancy, and a frequent overlap with preeclampsia. We report the case of a 33-year-old woman with normal kidney function, referred in the 14th gestational week of her second pregnancy, due to nephrotic proteinuria and macroscopic hematuria. The baby’s growth was normal. The patient reported episodes of macrohematuria one year previously. A kidney biopsy performed at 18 gestational weeks confirmed IgA nephropathy, associated with extensive podocyte damage. Treatment with steroids and tacrolimus led to remission of proteinuria and a healthy baby, adequate for gestational age, was delivered at 34 gestational weeks and 6 days (premature rupture of membranes). Six months after delivery, proteinuria was about 500 mg per day, with normal blood pressure and kidney function. This case highlights the importance of timely diagnosis in pregnancy and underlines that good maternal and fetal outcomes can be achieved with appropriate treatment, even in complex or severe cases.

Publisher

MDPI AG

Subject

General Medicine

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