孤立性右肺动脉发育不全伴右上叶发育不全,右下叶支气管扩张伴腹腔轴动脉供应异常,静脉引流正常。

A. Chaudhry, M. Rathore, Banavaliker Jn
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引用次数: 3

摘要

孤立性单侧肺动脉缺失(UAPA)是一种罕见的先天性异常。当在婴儿期发现时,这种情况通常与心血管缺陷有关,而心血管缺陷更常与左肺动脉发育不全有关。孤立性右肺动脉发育不全的患者存活至成年,症状极少或无症状,在胸片上被偶然诊断。我们报告一个19岁的女性患者谁提出了我们与反复咯血。她从四岁起就有症状了。我们报告罕见的右侧UAPA,右上肺叶发育不全和右下肺叶支气管扩张,伴有乳糜轴供血异常的右肺。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolated right pulmonary artery agenesis with agenesis of right upper lobe and bronchiectasis of right lower lobe with anomalous arterial supply from celiac axis with normal venous drainage.
Isolated unilateral absence of pulmonary artery (UAPA) is a rare congenital anomaly. When detected in infancy, the condition is commonly associated with cardiovascular defects which are more frequently associated with left pulmonary artery agenesis. Patients with isolated right pulmonary artery agenesis survive into adulthood with minimal or no symptoms and are diagnosed incidentally on the chest radiographs. We report a case of a 19-year-old female patient who presented to us with recurrent haemoptysis. She was symptomatic since the age of four years. We report the rare occurrence of UAPA on right side, agenesis of right upper lobe and bronchiectasis of right lower lobe with anomalous arterial supply of right lung from coeliac axis in this patient.
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