Coexistence of Autosomal Dominant Polycystic Kidney Disease and Amyloidosis in a Patient With Nephrotic-range Proteinuria

被引：0

作者：

Yenigun, Ezgi Coskun ^{[1
]}

Dede, Fatih ^{[1
]}

Ozkayar, Nihal ^{[1
]}

Turgut, Didem ^{[1
]}

Piskinpasa, Serhan Vahit ^{[1
]}

Ozturk, Ramazan ^{[1
]}

Koc, Eyup ^{[1
]}

Odabas, Ali Riza ^{[1
]}

机构：

[1] Ankara Numune Training & Res Hosp, Dept Nephrol, TR-06100 Ankara, Turkey

来源：

IRANIAN JOURNAL OF KIDNEY DISEASES | 2014年 / 8卷 / 03期

关键词：

amyloidosis; nephrotic syndrome; polycystic kidney disease; proteinuria;

D O I：

暂无

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

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.

引用

页码：243 / 245

页数：3

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