Sharma Vipul, Tudimilla Sonalika, Yerramshetty Mounika
Anesthesiology, Dr. D.Y. Patil Medical College, Hospital and Research Centre, Dr. D.Y. Patil Vidyapeeth (Deemed to be University), Pune, IND.
Cureus. 2024 Oct 5;16(10):e70886. doi: 10.7759/cureus.70886. eCollection 2024 Oct.
Coarctation of the aorta (CoA) accounts for a small percentage of all congenital heart diseases (CHD) and occurs with a rare incidence in live births. It is a frequently diagnosed cardiac defect in infancy, though some patients present later with severe complications and reduced life expectancy. Heterotaxy syndrome is marked by abnormal lateralization of abdominal and thoracic organs, including the cardiac atria. Cardiovascular anomalies are the primary cause of morbidity in children with heterotaxy syndrome. Early suspicion and accurate diagnosis enable a more focused and effective approach to treatment. This case report seeks to review the literature on this rare and remarkable subset of developmental anomalies to inform the reader about the various modes of presentation, clinical manifestations, and surgical and anesthetic management. Here, we present a unique case of a 14-year-old male with left isomerism scheduled for CoA and ventricular septal defect (VSD) repair. The following case report was previously presented at the World Conference of Anesthesia in March 2024, Singapore as a poster presentation.
主动脉缩窄(CoA)在所有先天性心脏病(CHD)中占比很小,在活产婴儿中的发病率很低。它是婴儿期常见的心脏缺陷,不过有些患者后来会出现严重并发症并缩短预期寿命。内脏反位综合征的特征是腹部和胸部器官(包括心房)的侧化异常。心血管异常是内脏反位综合征患儿发病的主要原因。早期怀疑和准确诊断有助于采取更有针对性和有效的治疗方法。本病例报告旨在回顾关于这一罕见且显著的发育异常子集的文献,以便让读者了解其各种表现形式、临床表现以及手术和麻醉管理。在此,我们介绍一例独特的病例,一名14岁男性,患有左位异构,计划进行主动脉缩窄和室间隔缺损(VSD)修复手术。以下病例报告曾于2024年3月在新加坡举行的世界麻醉大会上以海报形式展示。