article information

International Journal of Cardiovascular Practice: Vol.4, issue 4; 134-135
published online: December 05, 2019
article type: Case Report
received: October 05, 2019
accepted: November 07, 2019
DOI: https://doi.org/10.29252/ijcp-27360
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Pulmonary Capillary Hemangiomatosis: A Rare Cause of Pulmonary Arterial Hypertension, Presenting as Supraventricular Tachycardia

authors:

avatar Ganganpalli Dattaprasad 1 , avatar Umesh Kumar Chandra 1 , * , avatar Sumit Kumar Vishwakarma 1 , avatar V.P. Pandey 1 , avatar Sanjay Dubey 1

Department of Medicine, MGM Medical College Indore, MP, India

how to cite: Dattaprasad G, Chandra U K, 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. 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.

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