肾病综合征
医学
微量白蛋白尿
蛋白尿
肾功能
内科学
肾脏疾病
儿科
肾
入射(几何)
胃肠病学
物理
光学
作者
Richard Hull,David Goldsmith
出处
期刊:BMJ
[BMJ]
日期:2008-05-22
卷期号:336 (7654): 1185-1189
被引量:312
标识
DOI:10.1136/bmj.39576.709711.80
摘要
The nephrotic syndrome is one of the best known presentations of adult or paediatric kidney disease. The term describes the association of (heavy) proteinuria with peripheral oedema, hypoalbuminaemia, and hypercholesterolaemia (box 1). Protein in the urine (“coagulable urine”) was first described in 1821, 15 years before Richard Bright’s celebrated series of descriptions of “albuminous urine.”1
#### Box 1 Diagnostic criteria for nephrotic syndrome
Nephrotic syndrome has an incidence of three new cases per 100 000 each year in adults.2 It is a relatively rare way for kidney disease to manifest compared with reduced kidney function or microalbuminuria as a complication of systemic diseases, such as diabetes and raised blood pressure.3
#### Summary points
Patients with nephrotic syndrome can present to primary or secondary care with diverse symptoms that reflect the primary process or with one of the many systemic complications of the syndrome.4 Although nephrotic syndrome is relatively common in renal practice, it is seen only rarely in primary or secondary care. This can result in a delayed or overlooked diagnosis, especially as many other conditions have similar symptoms. For example, severe peripheral (leg) oedema is seen in congestive cardiac failure, hypoalbuminaemia can be caused …
科研通智能强力驱动
Strongly Powered by AbleSci AI