血栓性微血管病
医学
微血管病
入射(几何)
造血干细胞移植
重症监护医学
内科学
移植
疾病
光学
物理
内分泌学
糖尿病
作者
Mohamed Elemary,Waleed Sabry,Jerard Seghatchian,Hadi Goubran
标识
DOI:10.1016/j.transci.2019.04.022
摘要
Transplant-associated thrombotic microangiopathy (TA-TMA) is one of the early endothelial complications post Hematopoietic Stem Cell Transplant (HSCT). Several mechanisms during HSCT can contribute to systemic capillary endothelial damage which can lead to TA-TMA among other complications as capillary leak syndrome or engraftment syndrome. Early diagnosis of TA-TMA contributes a challenge due to overlapping clinical manifestations and the absence of specific diagnostic criteria. Incidence is greatly variable between 1–76% according to risk factors of patients and the definition used to confirm the diagnosis. The mortality rates in patients who develop severe TA-TMA are in excess of 80%. Early treatment improves the outcome. This review outlines the diagnostic challenges and therapeutic options for TA-TMA.
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