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肺动脉高压合并单侧肺动脉缺如及冠状动脉-肺动脉瘘:1例报告并文献复习

Pulmonary hypertension complicating unilateral absence of pulmonary artery and coronary-pulmonary artery fistula: Report of a case and review of the literature.

作者信息

Lin Chen-Chieh, Wu Cho-Kai, Kuo Ping-Hung

机构信息

Department of Internal Medicine National Taiwan University Hospital and National Taiwan University College of Medicine Taipei Taiwan.

出版信息

Pulm Circ. 2022 Oct 1;12(4):e12160. doi: 10.1002/pul2.12160. eCollection 2022 Oct.

Abstract

This is a case report of a 53-year-old woman who presented to our hospital in 2011 with an intermittent cough and dyspnea for 5 years. The chest X-ray showed a prominent left hilum and a smaller right lung. Computed tomography (CT) of the chest confirmed the absence of the right pulmonary artery (PA) and the right cardiac catheterization showed a mean PA pressure of 34 mmHg. Concomitant asthma and unilateral absence of pulmonary artery (UAPA) were diagnosed. In the following years, her functional class remained stable under medications including low-dose sildenafil and spironolactone. In 2020, she developed mild intermittent chest tightness and the coronary angiography showed a fistula between the proximal left circumflex coronary artery and right pulmonary circulation. She declined further intervention for her coronary-pulmonary artery fistula (CPAF) and her symptoms improved spontaneously. To our knowledge, only 16 similar cases with combined UAPA and CPAF in adults have been reported in the literature, of which, pulmonary hypertension was documented in nine patients (56.3%).

摘要

这是一例53岁女性的病例报告,该患者于2011年因间歇性咳嗽和呼吸困难5年就诊于我院。胸部X线显示左肺门突出,右肺较小。胸部计算机断层扫描(CT)证实右肺动脉(PA)缺如,右心导管检查显示平均肺动脉压为34 mmHg。诊断为合并哮喘和单侧肺动脉缺如(UAPA)。在随后的几年里,在使用包括低剂量西地那非和螺内酯在内的药物治疗下,她的功能分级保持稳定。2020年,她出现轻度间歇性胸闷,冠状动脉造影显示左回旋支冠状动脉近端与右肺循环之间存在瘘管。她拒绝了对其冠状动脉-肺动脉瘘(CPAF)的进一步干预,症状自行改善。据我们所知,文献中仅报道了16例成人合并UAPA和CPAF的类似病例,其中9例(56.3%)记录有肺动脉高压。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/612f/9679234/29e33295233b/PUL2-12-e12160-g001.jpg

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