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International Journal of Cardiovascular Practice
Pulmonary Capillary Hemangiomatosis: A Rare Cause of Pulmonary Arterial Hypertension, Presenting as Supraventricular Tachycardia
Author(s):
Ganganpalli Dattaprasad1, Umesh Kumar Chandra 1,*, Sumit Kumar Vishwakarma1, V.P. Pandey1, Sanjay Dubey11Department of Medicine, MGM Medical College Indore, MP, India
*Corresponding Author: Corresponding author: Department of Medicine, MGMMedical College Indore, MP, India. E-mail: Email: [email protected]
Published online:Dec 05, 2019
Article type:Case Report
Received:Oct 05, 2019
Accepted:Nov 07, 2019
How to Cite:Dattaprasad G, Chandra UK, Kumar Vishwakarma S, Pandey V, Dubey S. Pulmonary Capillary Hemangiomatosis: A Rare Cause of Pulmonary Arterial Hypertension, Presenting as Supraventricular Tachycardia. Int J Cardiovasc Pract. 2019;4(4):e130565. doi: 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.
Copyright
© 2019, International Journal of Cardiovascular Practice. This open-access article is available under the Creative Commons Attribution-NonCommercial 4.0 (CC BY-NC 4.0) International License (https://creativecommons.org/licenses/by-nc/4.0/), which allows for the copying and redistribution of the material only for noncommercial purposes, provided that the original work is properly cited.
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