Thrombotic microangiopathies: Similar presentations, different therapies

被引：6

作者：

Appel, Gerald B. ^{[1
,2
]}

机构：

[1] New York Presbyterian Hosp, Glomerular Ctr, New York, NY 10065 USA

[2] Columbia Univ, Coll Phys & Surg, New York, NY 10027 USA

来源：

CLEVELAND CLINIC JOURNAL OF MEDICINE | 2017年 / 84卷 / 02期

关键词：

HEMOLYTIC-UREMIC SYNDROME; ANTIPHOSPHOLIPID-ANTIBODY-SYNDROME; COMPLEMENT INHIBITOR ECULIZUMAB; VON-WILLEBRAND-FACTOR; THROMBOCYTOPENIC PURPURA; PLASMA-EXCHANGE; RECURRENT MISCARRIAGE; PATHOGENESIS; RITUXIMAB; GERMANY;

D O I：

10.3949/ccjm.84gr.17001

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Thrombotic thrombocytopenic purpura, Shiga toxin hemolytic uremic syndrome, atypical hemolytic uremic syndrome, and antiphospholipid syndrome are thrombotic microangiopathies that present similarly but arise from different causes. Management depends on distinguishing them promptly and providing targeted therapy.

引用

页码：114 / 130

页数：8

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