Remembering the Basics: A Patient with Sickle Cell Disease and Proteinuria

被引：0

作者：

Ozbalak, Ezgi Pinar ^{[1
]}

Mirioglu, Safak ^{[1
]}

Sahin, Ezgi ^{[1
]}

Ozluk, Yasemin ^{[2
]}

Ucar, Ali Riza ^{[3
]}

Yazici, Halil ^{[3
]}

Kilicaslan, Isin ^{[2
]}

Kalayoglu-Besisik, Sevgi ^{[4
]}

机构：

[1] Istanbul Univ, Istanbul Sch Med, Dept Internal Med, Istanbul, Turkey

[2] Istanbul Univ, Istanbul Sch Med, Dept Pathol, Istanbul, Turkey

[3] Istanbul Univ, Istanbul Sch Med, Dept Internal Med, Div Nephrol, Istanbul, Turkey

[4] Istanbul Univ, Istanbul Sch Med, Dept Internal Med, Div Hematol, Istanbul, Turkey

来源：

TURKISH JOURNAL OF NEPHROLOGY | 2019年 / 28卷 / 02期

关键词：

Sickle cell disease; sickle cell nephropathy; proteinuria; NEPHROTIC SYNDROME; GLOMERULOPATHY; NEPHROPATHY;

D O I：

10.5152/turkjnephrol.2019.3198

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：

Patients with sickle cell disease (SCD) tend to develop many renal abnormalities, including concentration defect, renal papillary necrosis, and glomerulopathy that often presents with proteinuria. We report a case of a patient who presented with sickle cell crisis and proteinuria. A diagnosis of SCD glomerulopathy was confirmed with renal biopsy. Treatment with angiotensin-converting enzyme inhibitor was initiated, and proteinuria rapidly reduced to 0.27 g/day. It is crucial for a clinician to recognize this important complication and take necessary precautions to delay progression to end-stage renal disease.

引用

页码：154 / 156

页数：3

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