因肺动静脉畸形形成导致的肺动脉高压消退。
Regression of pulmonary artery hypertension due to development of a pulmonary arteriovenous malformation.
作者信息
Hasan Ashfaq, Sastry B K S, Aleem M A, Reddy Gokul, Mahmood Syed
机构信息
Professor and Head, Department of Pulmonary Medicine, Deccan College of Medical Sciences/Owaisi Hospital, Hyderabad, India; Consultant Pulmonologist, Care Institute of Medical Sciences (Banjara), Hyderabad, India.
Consultant Cardiologist, Care Institute of Medical Sciences (Nampally), Hyderabad, India.
出版信息
Indian Heart J. 2014 Sep-Oct;66(5):535-8. doi: 10.1016/j.ihj.2014.09.001. Epub 2014 Sep 24.
Abstract
Idiopathic Pulmonary Hypertension (IPAH) is characterized by elevated pulmonary arterial pressure in the absence of an identifiable underlying cause. The condition is usually relentlessly progressive with a short survival in the absence of treatment.(1) We describe a patient of IPAH in whom the pulmonary artery pressures significantly abated with complete disappearance of symptoms, following spontaneous development of a pulmonary arterio-venous malformation (PAVM).
摘要
特发性肺动脉高压（IPAH）的特征是在没有可识别的潜在病因的情况下肺动脉压力升高。在没有治疗的情况下，这种疾病通常会持续进展，生存期较短。（1）我们描述了一名特发性肺动脉高压患者，该患者在自发形成肺动静脉畸形（PAVM）后，肺动脉压力显著降低，症状完全消失。
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