| Literature DB >> 21972386 |
Delphine Natali1, Barbara Girerd1, David Montani1, Florent Soubrier2, Gérald Simonneau1, Marc Humbert1, Olivier Sitbon3.
Abstract
We report a case of pulmonary arterial hypertension (PAH) occurring in a patient with Cowden syndrome with a mutation in the phosphatase and tensin (PTEN) tumor suppressor gene, in the context of exposure to the appetite suppressant dexfenfluramine. Anorexigen exposure is known to be a risk factor for PAH. However, the role of PTEN in cell function and the development of pulmonary vascular remodeling and histopathologic signs of PAH in mice with a Pten depletion in smooth muscle cells suggest that the association of PAH and Cowden syndrome may be relevant. In this case report, we hypothesize that PTEN mutations may be a predisposing factor for the development of PAH, with anorexigen exposure as a potential trigger.Entities:
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Year: 2011 PMID: 21972386 DOI: 10.1378/chest.10-2588
Source DB: PubMed Journal: Chest ISSN: 0012-3692 Impact factor: 9.410