دورية أكاديمية

Pulmonary arterial hypertension in a patient with Cowden syndrome and anorexigen exposure.

التفاصيل البيبلوغرافية
العنوان: Pulmonary arterial hypertension in a patient with Cowden syndrome and anorexigen exposure.
المؤلفون: Natali D, Girerd B, Montani D, Soubrier F, Simonneau G, Humbert M, Sitbon O, Natali, Delphine, Girerd, Barbara, Montani, David, Soubrier, Florent, Simonneau, Gérald, Humbert, Marc, Sitbon, Olivier
المصدر: CHEST; Oct2011, Vol. 140 Issue 4, p1066-1068, 3p
مستخلص: 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. [ABSTRACT FROM AUTHOR]
Copyright of CHEST is the property of American College of Chest Physicians and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:00123692
DOI:10.1378/chest.10-2588