肺毛细血管瘤病:肺动脉高压的罕见病因,表现为室上性心动过速

Ganganpalli Dattaprasad, U. Chandra, S. Vishwakarma, V. Pandey, S. Dubey
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引用次数: 0

摘要

肺毛细血管瘤病是一种罕见的肺泡间隔毛细血管增生疾病,可导致肺动脉高压,类似肺静脉闭塞性疾病,患病率不到百万分之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pulmonary Capillary Hemangiomatosis: A Rare Cause of Pulmonary Arterial Hypertension, Presenting as Supraventricular Tachycardia
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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