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

AuthorGanganpalli Dattaprasaden
AuthorUmesh Kumar Chandraen
AuthorSumit Kumar Vishwakarmaen
AuthorV.P. Pandeyen
AuthorSanjay Dubeyen
Issued Date2019-10-31en
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.en
DOIhttps://doi.org/10.29252/ijcp-27360en
KeywordPulmonary Veno-occlusiveen
KeywordDiseaseen
KeywordPulmonary Capillaryen
KeywordHemangiomaen
PublisherBrieflandsen
TitlePulmonary Capillary Hemangiomatosis: A Rare Cause of Pulmonary Arterial Hypertension, Presenting as Supraventricular Tachycardiaen
TypeCase Reporten

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