4.3 Review

Pathology Consultation on the Diagnosis and Treatment of Thrombotic Microangiopathies (TMAs)

期刊

AMERICAN JOURNAL OF CLINICAL PATHOLOGY
卷 145, 期 2, 页码 158-165

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/ajcp/aqv086

关键词

Thrombotic microangiopathy (TMA); Thrombotic thrombocytopenic purpura (TTP); Hemolytic uremic syndrome (HUS); Microangiopathic hemolytic anemia (MAHA)

向作者/读者索取更多资源

Objectives: Pathologists specializing in transfusion medicine, apheresis medicine, and/or coagulation are often consulted by clinicians to reach a diagnosis for patients with thrombotic microangiopathy (TMA), so that disease-specc, often life-saving therapy can be initiated as promptly as possible. Methods: This article describes how to proceed when treating a patient with TMA. The differential diagnosis is broad and potentially very challenging. Thrombotic thrombocytopenic purpura (TTP), atypical hemolytic uremic syndrome (aHUS), and typical hemolytic uremic syndrome (HUS) are three such TMAs that require timely diagnosis and treatment. Results: TTP is treated with daily therapeutic plasma exchange (TPE) and commonly with adjunctive immunosuppressive therapy, while aHUS may initially be managed with TPE but is best controlled with eculizumab once a presumptive diagnosis is made. TPE has no proven role in typical HUS, which is most commonly treated with supportive measures only. Conclusions: Prompt and accurate diagnosis of TMA sub-types optimizes treatment and improves patient outcomes.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据