病例报告：慢性复发性单侧肺部感染：先天性单侧肺动脉缺如的结果
Case Report: Chronic Recurrent Unilateral Pulmonary Infection: Result of Congenital Unilateral Agenesis of Pulmonary Artery.
作者信息
Al Jabbari Odeaa, Abu Saleh Walid K, Ramchandani Mahesh, Scheinin Scott
机构信息
Houston Methodist DeBakey Heart & Vascular Center, Houston Methodist Hospital, Houston, Texas.
出版信息
Methodist Debakey Cardiovasc J. 2016 Jan-Mar;12(1):48-50. doi: 10.14797/mdcj-12-1-48.
Abstract
Unilateral agenesis of the pulmonary artery (UAPA) is a rare congenital anomaly. This report describes a 52-year-old female who gave a long history of chronic, recurrent, left-sided pulmonary infections related to UAPA. For many years, she was managed medically but the infection continued to recur. She eventually underwent left pneumonectomy and made a good recovery.
摘要
单侧肺动脉缺如（UAPA）是一种罕见的先天性异常。本报告描述了一名52岁女性，她有长期慢性、复发性左侧肺部感染病史，与单侧肺动脉缺如有关。多年来，她接受药物治疗，但感染仍持续复发。她最终接受了左肺切除术，恢复良好。
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