Thrombotic Thrombocytopenic Purpura in Childhood

被引:15
作者
Bouw, Maria C. [1 ]
Dors, Natasja [2 ]
van Ommen, Heleen [2 ]
Ramakers-van Woerden, Nicole L. [1 ]
机构
[1] Meander Med Ctr, Dept Paediat, Amersfoort, Netherlands
[2] Emma Childrens Hosp, Acad Med Ctr, Dept Paediat Haematol, Amsterdam, Netherlands
关键词
ADAMTS13; haemolytic uraemic syndrome; thrombotic microangiopathy; thrombotic thrombocytopenic purpura; von Willebrand factor cleaving protease; HEMOLYTIC-UREMIC SYNDROME; VON-WILLEBRAND-FACTOR; FACTOR-CLEAVING PROTEASE; PLASMA-EXCHANGE; ADAMTS13; ACTIVITY; FACTOR-VIII; RITUXIMAB; CYCLOSPORINE; SPLENECTOMY; ANTIBODIES;
D O I
10.1002/pbc.22094
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Thrombotic thrombocytopenic puripura (TTP) is a rare disease, especially in childhood, and has a high mortality rate in the absence of appropriate treatment. it is characterised by microangiopathic haemolytic anaemia and consumptive thrombocytopenia. TTP may be difficult to distinguish from haemolytic uraemic syndrome (HUS) because of similar clinical manifestations and laboratory findings. In the past, TTP and HUS have often been considered to represent variable expressions of a single entity. Our increased understanding of the pathogenesis of TTP has in turn resulted in significant improvements in its treatment and outcomes. Several immunomodulating agents are currently being Used with variable outcomes. Pediatr Blood Cancer 2009;53:537-542. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:537 / 542
页数:6
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