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Pulmonary Capillary Hemangiomatosis: A Rare Cause of Pulmonary Arterial Hypertension, Presenting as Supraventricular Tachycardia

With a prevalence of less than 1/million, Pulmonary Capillary Hemangiomatosis is a rare disorder of capillary proliferation in the alveolar septae leading to pulmonary arterial hypertension and mimics pulmonary veno-occlusive disease.

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Ganganpalli Dattaprasad, Umesh Kumar Chandra, Sumit Kumar Vishwakarma, V.P. Pandey, Sanjay Dubey
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Shahid Beheshti University of Medical Sciences 2019-12-01
Cyfres:International Journal of Cardiovascular Practice
Mynediad Ar-lein:http://journals.sbmu.ac.ir/ijcp/article/view/27360
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