Uncorrected Tetralogy of Fallot With Pulmonary Atresia in an Adult

Q4 Medicine
Charlie J. Sang III MD , Lunise Benjamin DNP , Elman G. Frantz MD , Michael Yeung MD
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Abstract

Background

Management of tetralogy of Fallot with pulmonary atresia (ToF-PA) in adults is not well established.

Case

A 37-year-old woman with ToF-PA presented with dyspnea. Left and right heart catheterization revealed a large major aortopulmonary collateral artery (MAPCA) to the left pulmonary artery supplying confluent pulmonary arteries and with normal pulmonary vascular resistance. She underwent fenestrated ventricular septal defect closure, ligation of the MAPCA, and right ventricle–to–pulmonary artery conduit placement. She developed acute right heart failure, with distal conduit stenosis with the residual MAPCAs. A 26 × 12 mm stent was deployed, with relief of conduit stenosis. The MAPCAs were closed with vascular plug and coils.

Discussion

Surgical repair can be recommended with confluent pulmonary arteries of adequate size, MAPCAs in which unifocalization or ligation/coiling can occur, and absence of severe pulmonary vascular disease. Surgery in adults may contribute significantly to mortality, with unclear benefit.

Take-Home Messages

Unrepaired ToF-PA in adults is rare, and careful consideration must be given to each patient given the lack of standardized treatment protocols. Multidisciplinary teams are essential for preoperative planning and management of postoperative complications.
未纠正的法洛四联症合并肺闭锁一例成人
背景:成人法洛四联症合并肺闭锁(ToF-PA)的治疗尚不明确。37岁女性ToF-PA患者表现为呼吸困难。左、右心导管检查显示左肺动脉有一条大的主肺动脉副支(MAPCA),供应肺动脉合流,肺血管阻力正常。她接受了开窗室间隔缺损闭合、MAPCA结扎和右心室至肺动脉导管置入术。她出现了急性右心衰,远端导管狭窄伴有残留的MAPCAs。放置26 × 12 mm支架,缓解导管狭窄。用血管塞和线圈封闭mapca。对于足够大小的合流肺动脉、可发生集中或结扎/盘绕的MAPCAs以及无严重肺血管疾病的患者,可推荐手术修复。成人手术可能对死亡率有显著影响,但益处尚不清楚。成人ToF-PA未修复是罕见的,由于缺乏标准化的治疗方案,必须仔细考虑每个患者。多学科团队对于术前计划和术后并发症的处理至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JACC. Case reports
JACC. Case reports Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.30
自引率
0.00%
发文量
404
审稿时长
17 weeks
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