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

AuthorGanganpalli Dattaprasad
AuthorUmesh Kumar Chandra
AuthorSumit Kumar Vishwakarma
AuthorV.P. Pandey
AuthorSanjay Dubey
Issued Date2019-10-31
AbstractWith 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.
DOIhttps://doi.org/10.29252/ijcp-27360
KeywordPulmonary Veno-occlusive
KeywordDisease
KeywordPulmonary Capillary
KeywordHemangioma
PublisherBrieflands
TitlePulmonary Capillary Hemangiomatosis: A Rare Cause of Pulmonary Arterial Hypertension, Presenting as Supraventricular Tachycardia
TypeCase Report
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