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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.
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Shahid Beheshti University of Medical Sciences
2019-12-01
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| Col·lecció: | International Journal of Cardiovascular Practice |
| Accés en línia: | http://journals.sbmu.ac.ir/ijcp/article/view/27360 |
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