法洛四联症合并主动脉-肺副支同时根治的临床分析

K. Kuatbekov, A. Egizekov, D.T. Musagaliev, T.V. Maslov, E.T. Sydykov, A. V. Mishin, N. Baizhigitov, B. Suieubekov
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摘要

法洛四联症(TOF)合并主动脉-肺侧支动脉(MAPCA)是一种严重的先天性心脏缺陷,是由心脏畸形三联症合并小循环系统血管异常引起的。迄今为止,对于联合畸形的根治性手术矫正,没有统一的公认标准。本文报道一名8个月大的儿童同时进行TOF和血管内封堵MAPCA的临床病例。根据一项大型研究的证据基础,我们的患者属于TOF矫正后首先采用MAPCA治疗方式的群体,该治疗方式38%无效,导致MAPCA闭塞的手术方式。选择两种病理同时手术治疗的方式,使术后风险降至最低,取得良好的临床效果。
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CLINICAL CASE OF SIMULTANEOUS RADICAL TREATMENT OF TETRALOGY OF FALLOT WITH MAJOR AORTOPULMONARY COLLATERAL ARTERIES
Tetralogy of Fallot (TOF) combined with major aortopulmonary collateral arteries (MAPCA) is a severe congenital heart defect due to the combination of a triad of cardiac malformation withan additional vascular anomaly of the small circulatory system. To date, there is no single accepted standard in which sequence and according to which criteria radical surgical correction of combined anomalies is indicated. This paper describes a clinical case of simultaneous opentreatment of TOF and endovascular occlusion of the MAPCA in an 8-month old child. Based onthe evidence base of a large study, our patient belonged to the group where after TOF correction the therapeutic way of MAPCA treatment was used at first, which was ineffective in 38% and led to surgical methods of MAPCA occlusion. Choosing the way of simultaneous simultaneoussurgical treatment of two pathologies allowed us to minimize postoperative risks and achievegoodclinical results.
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