NEPHROTIC SYNDROME IN THE FRAMES OF POLYCYSTIC KIDNEY DISEASE: DESCRIPTION OF TWO CASES
https://doi.org/10.24884/1561-6274-2011-15-2-84-88
Abstract
Two cases of nephrotic syndrome in patients suffering from autosomaldominant polycystic kidney disease is described. During nephrobiopsy were the following morphological diagnoses were stated: IgA-nephropathy and membranous nephropathy. Isolated appointment of ACE inhibitor did not lead to a reduction in proteinuria, but its combination with methyl-prednisolone and cytotoxic drugs for different periods allowed significantly reduce proteinuria and stabilize renal function. Our cases showed the appropriateness of the nephrobiopsy in patients with polycystic kidney disease and nephrotic syndrome in order to determine further management treatment and prevention of progression of renal failure.
About the Authors
K. S. KOMISSAROV
Белорусская медицинская академия последипломного образования
Belarus
Belarus
M. V. DMITRIEVA
1-ая городская клиническая больница г. Минска
Belarus
Belarus
t. N. TSVIRKO
1-ая городская клиническая больница г. Минска
Belarus
Belarus
K. S. EFREMOV
1-ая городская клиническая больница г. Минска
Belarus
Belarus
V. S. PILOTOVICH
Белорусская медицинская академия последипломного образования
Belarus
Belarus
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Review
For citations:
KOMISSAROV K.S., DMITRIEVA M.V., TSVIRKO t.N., EFREMOV K.S., PILOTOVICH V.S. NEPHROTIC SYNDROME IN THE FRAMES OF POLYCYSTIC KIDNEY DISEASE: DESCRIPTION OF TWO CASES. Nephrology (Saint-Petersburg). 2011;15(2):84-88. (In Russ.) https://doi.org/10.24884/1561-6274-2011-15-2-84-88
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