一例成人左冠状动脉起源于肺动脉异常的临床病例(Bland-White-Garland综合征)

A. O. Povoroznyi, E. A. Zakharyan, P. Maksimova, J. T. Keremov, O. A. Kazanceva
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引用次数: 0

摘要

高光。本文提出了一个独特的临床病例的患者先天性心脏缺陷被称为白-白-花环综合征诊断在成年期。Takeuchi修复术(建立肺内隧道)用于治疗该缺陷。左冠状动脉起源于肺动脉异常(Bland-White-Garland综合征)是一种罕见但严重的病理,需要立即手术治疗。现代诊断方法(非侵入性和侵入性)的使用导致这种综合征的患病率更高,不仅在幼儿期诊断出来,而且在成年期也诊断出来。记录每个病例并选择最佳治疗策略将增加对该病理的了解并降低高死亡率。本文报道一例慢性心力衰竭的临床特征掩盖了该综合征,长期未被诊断出来的成年患者。Takeuchi修复术(创建肺内隧道)用于治疗该年龄组患者的这种极其罕见的缺陷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A clinical case of an anomalous origin of the left coronary artery from the pulmonary artery (Bland-White-Garland syndrome) in an adult patient
Highlights. The paper presents a unique clinical case of patient with congenital heart defect known as Bland-White-Garland syndrome diagnosed in the adulthood. Takeuchi repair (creation an intrapulmonary tunnel) was carried out to treat this defect.Background. An anomalous origin of the left coronary artery from the pulmonary artery (Bland-White-Garland syndrome) is an uncommon but severe pathology that requires immediate  surgical  treatment.  The  use  of  modern  diagnostic  methods  (both non-invasive and invasive) has resulted in higher prevalence of this syndrome, diagnosed not only in an early childhood, but also in adulthood. Recording each medical case and choosing an optimal treatment strategy will increase knowledge of this pathology and reduce the high risk of mortality. The paper presents a clinical case of this syndrome in an adult patient who had remained undiagnosed for a long time as the syndrome was masked under the clinical features of chronic heart failure. Takeuchi repair (creation an intrapulmonary tunnel) was carried out to treat this extremely rare defect for a patient of this age group.
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