مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

MASSIVE PROTEINURIA AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE A RARE COINCIDENCE

Pages

  73-76

Abstract

 Autosomal dominant polycystic kidney disease (ADPKD) with nephrotic syndrome is a rare coincidence. Among 19 reported cases since 1972, focal glomerulosclerosis is the dominant reported pathology. Here, we report the 6th case of FOCAL SEGMENTAL GLOMERULOSCLEROSIS with ADPKD. A 29-year-old man with a history of APCDK presented with massive PROTEINURIA. He had a history of concurrent leptospirosis and brucellosis, and trace PROTEINURIA and mild hypertension had been diagnosed 4 years earlier. Urine study showed PROTEINURIA (21 g/d) and hematuria. Kidney biopsy report was compatible with focal and segmental sclerosis. The patient received prednisolone and cyclosporine. After 4 months, PROTEINURIA decreased to 600 mg/d. Patients with ADPKD who show massive PROTEINURIA should undergo kidney biopsy. It is possible that different mutations in these patients could clarify the nature of this coincidence.

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  • Cite

    APA: Copy

    SAVAJ, SHOKOUFEH, PARVIN, MAHMOUD, & SAVOJ, JAVAD. (2012). MASSIVE PROTEINURIA AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE A RARE COINCIDENCE. IRANIAN JOURNAL OF KIDNEY DISEASES (IJKD), 6(1), 73-76. SID. https://sid.ir/paper/309312/en

    Vancouver: Copy

    SAVAJ SHOKOUFEH, PARVIN MAHMOUD, SAVOJ JAVAD. MASSIVE PROTEINURIA AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE A RARE COINCIDENCE. IRANIAN JOURNAL OF KIDNEY DISEASES (IJKD)[Internet]. 2012;6(1):73-76. Available from: https://sid.ir/paper/309312/en

    IEEE: Copy

    SHOKOUFEH SAVAJ, MAHMOUD PARVIN, and JAVAD SAVOJ, “MASSIVE PROTEINURIA AND AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE A RARE COINCIDENCE,” IRANIAN JOURNAL OF KIDNEY DISEASES (IJKD), vol. 6, no. 1, pp. 73–76, 2012, [Online]. Available: https://sid.ir/paper/309312/en

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