Pulmonary Capillary Hemangiomatosis: A Rare Cause of Pulmonary Arterial Hypertension, Presenting as Supraventricular Tachycardia
International Journal of Cardiovascular Practice,
Vol. 4 No. 4 (2019),
31 December 2019
,
Page 134-135
https://doi.org/10.29252/ijcp-27360
Abstract
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.How to Cite
Dattaprasad, G., Chandra, U. K., Vishwakarma, S. K., Pandey, V., & Dubey, S. (2019). Pulmonary Capillary Hemangiomatosis: A Rare Cause of Pulmonary Arterial Hypertension, Presenting as Supraventricular Tachycardia. International Journal of Cardiovascular Practice, 4(4), 134–135. https://doi.org/10.29252/ijcp-27360
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