Crystalline Nephropathies

被引:79
作者
Herlitz, Leal C. [1 ]
D'Agati, Vivette D.
Markowitz, Glen S.
机构
[1] Columbia Univ, Med Ctr, Dept Pathol & Cell Biol, New York, NY 10032 USA
关键词
ACUTE PHOSPHATE NEPHROPATHY; IRREVERSIBLE RENAL-FAILURE; CHAIN PROXIMAL TUBULOPATHY; ADULT FANCONI-SYNDROME; STORING HISTIOCYTOSIS; TOXOPLASMA ENCEPHALITIS; INDINAVIR NEPHROPATHY; UNDERRECOGNIZED CAUSE; CLINICAL COURSE; V-DOMAIN;
D O I
10.5858/arpa.2011-0565-RA
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
100118 [医学信息学]; 100208 [临床检验诊断学];
摘要
Context.-The kidney is a favored site for crystal deposition because of the high concentration of ions and molecules reached at the level of the renal tubules in the course of filtration. This review focuses on crystalline nephropathies in 4 broad categories: (1) dysproteinemia-associated, (2) drug-induced, (3) calcium-containing, and (4) metabolic or genetic. Objective.-To provide a framework for accurate identification of the diverse types of crystals encountered in the kidney in order to formulate an appropriate differential diagnosis and guide additional testing and treatment. Data Sources.-Review of pertinent published literature along with practical experience gained in a high-volume renal pathology laboratory. Conclusions.-Accurate identification of crystals encountered in the kidney is essential in detecting conditions ranging from hematologic malignancy to drug toxicity to metabolic disorders. Detailed clinical-pathologic correlation is needed to accurately diagnose the underlying cause of most crystalline nephropathies. (Arch Pathol Lab Med. 2012; 136: 713-720; doi: 10.5858/arpa.2011-0565-RA)
引用
收藏
页码:713 / 720
页数:8
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