Multifaceted Hemolytic Uremic Syndrome in Pediatrics

被引:4
作者
Nester, Carla M. [1 ,2 ]
机构
[1] Univ Iowa, Dept Internal Med, Rare Renal Dis Clin, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Pediat, Rare Renal Dis Clin, Iowa City, IA 52242 USA
关键词
Hemolytic uremic syndrome; STEC HUS; Atypical hemolytic uremic syndrome; Complement; THROMBOTIC THROMBOCYTOPENIC PURPURA; FACTOR-H AUTOANTIBODIES; ESCHERICHIA-COLI; PLASMA-EXCHANGE; COMPLEMENT; MUTATIONS; MICROANGIOPATHY; ECULIZUMAB; IMPACT; HUS;
D O I
10.1159/000346486
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hemolytic uremic syndromes can have devastating consequences in childhood. The common feature of a microangiopathic hemolytic anemia and thrombocytopenia associated with varying degrees of renal injury often creates diagnostic confusion. The inability to arrive at a definitive diagnosis quickly can lead to a delay in initiating renal-preserving and sometimes life-saving treatment. Currently, both the treatment plan and the prognosis vary substantially according to the presumed diagnosis. The availability of anti-complement therapy makes differentiating the cause of the hemolytic uremic syndrome particularly critical. Therefore, it is imperative that consideration be given to each of the possible syndromes at presentation in order to facilitate correct diagnosis and development of an appropriate treatment strategy for both the acute phase and for the long-term care of the patient. Copyright (C) 2013 S. Karger AG, Basel
引用
收藏
页码:86 / 92
页数:7
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