Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2102555 | Biology of Blood and Marrow Transplantation | 2013 | 11 Pages |
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.
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Authors
Christopher E. Dandoy, Russel Hirsch, Ranjit Chima, Stella M. Davies, Sonata Jodele,