| Literature DB >> 31097308 |
Mohamed Elemary1, Waleed Sabry2, Jerard Seghatchian3, Hadi Goubran2.
Abstract
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.Entities:
Keywords: Diagnosis; Management; TA-TMA; Transplant-associated thrombotic microangiopathy
Mesh:
Year: 2019 PMID: 31097308 DOI: 10.1016/j.transci.2019.04.022
Source DB: PubMed Journal: Transfus Apher Sci ISSN: 1473-0502 Impact factor: 1.764