| Literature DB >> 23891748 |
Christopher E Dandoy1, Russel Hirsch, Ranjit Chima, Stella M Davies, Sonata Jodele.
Abstract
Pulmonary hypertension (PH) is a potentially fatal complication of hematopoietic stem cell transplantation (HSCT). Given its nonspecific clinical presentation, it is likely that this clinical entity is underdiagnosed after HSCT. Data describing the incidence, risk factors, and etiology of PH in HSCT recipients are minimal. Physicians caring for HSCT recipients should be aware of this severe post-transplant complication because timely diagnosis and treatment may allow improved clinical outcomes. We summarize the pathophysiology, clinical presentation, diagnosis, and management of PH in HSCT recipients.Entities:
Keywords: Pulmonary arterial hypertension; Pulmonary hypertension; Pulmonary veno-occlusive disease; Thrombotic microangiopathy
Mesh:
Year: 2013 PMID: 23891748 DOI: 10.1016/j.bbmt.2013.07.017
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742