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Paper Information

Journal:   IRANIAN JOURNAL OF KIDNEY DISEASES (IJKD)   MAY 2014 , Volume 8 , Number 3; Page(s) 243 To 245.
 
Paper: 

COEXISTENCE OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE AND AMYLOIDOSIS IN A PATIENT WITH NEPHROTIC-RANGE PROTEINURIA (CASE REPORT)

 
 
Author(s):  YENIGUN EZGI COSKUN*, DEDE FATIH, OZKAYAR NIHAL, TURGUT DIDEM, PISKINPASA SERHAN VAHIT, OZTURK RAMAZAN, KOC EYUP, ODABAS ALI RIZA
 
* DEPARTMENT OF NEPHROLOGY, ANKARA NUMUNE RESEARCH AND EDUCATION HOSPITAL, ANKARA NUMUNE EGITIM VE ARASTIRMA HASTANESI NEFROLOJI KLINIGI, 06100, SAMANPAZARI, ANKARA, TURKEY
 
Abstract: 

Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disorder characterized by the development and growth of cysts in the kidneys. Non-nephritic-range proteinuria is a common presentation in ADPKD patients; however, nephrotic syndrome is a rare coincidence. A 52-year-old man is described who was diagnosed with secondary amyloidosis with ADPKD. To our knowledge, this is the first case of amyloidosis associated with frequently infected renal cysts. Patients with ADPKD who show massive proteinuria should be investigated in terms of concomitant glomerular disease.

 
Keyword(s): AMYLOIDOSIS, NEPHROTIC SYNDROME, POLYCYSTIC KIDNEY DISEASE, PROTEINURIA
 
References: 
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