Cavalle-Garrido T, Bernasconi A, Perrin D, Anderson R H
Division of Cardiology, Department of Pediatrics, Hospital for Sick Children, 555 University Avenue, Toronto, ON M5G 1X7, Canada.
Heart. 2007 Jan;93(1):100-6. doi: 10.1136/hrt.2006.093369. Epub 2006 Jun 28.
To determine the characteristic morphological features of hearts with concordant ventriculoarterial connections and parallel arterial trunks, and to provide unequivocally a method to describe their anatomy. DESIGN, METHODS AND PATIENTS: The entire cardiac database and cardiac pathological archive at the Hospital for Sick Children, Toronto, Ontario, Canada, was interrogated to identify all patients with concordant ventriculoarterial connections and parallel arterial trunks. The clinical records, autopsy reports and actual cardiac specimens of those who underwent autopsy, were reviewed.
8 cases meeting our criteria were identified. The infundibular anatomy was variable, including four hearts with bilateral infundibulums, three with subpulmonary infundibulums and one with bilaterally absent infundibulums. Considerable variability was also found in the type of atrial arrangement, along with the morphology of the atrioventricular junctions. The most common findings were the usual atrial arrangement (n = 5), left juxtaposition of the right atrial appendages (n = 3), an atrial septal defect (n = 6), univentricular atrioventricular connection (n = 5), ventricular septal defect (n = 8) and pulmonary obstruction (n = 4). In addition, five specimens had either a single coronary artery or two coronary arteries arising from the anticipated right coronary aortic sinus.
Concordant ventriculoarterial connections with parallel arterial trunks can be found in a variety of segmental combinations. An accurate diagnosis of these rare hearts can be achieved by detailed analysis of not only the ventriculoarterial connections but also the infundibular anatomy and the spatial relationship of the arterial trunks. Particular attention to the coronary arteries is warranted.
确定具有心室动脉连接一致和动脉干并行的心脏的特征性形态学特征,并明确提供一种描述其解剖结构的方法。
设计、方法和患者:对加拿大多伦多病童医院的整个心脏数据库和心脏病理档案进行查询,以识别所有具有心室动脉连接一致和动脉干并行的患者。对那些接受尸检者的临床记录、尸检报告和实际心脏标本进行了回顾。
确定了8例符合我们标准的病例。漏斗部解剖结构各异,包括4例双侧漏斗部的心脏、3例肺动脉下漏斗部的心脏和1例双侧无漏斗部的心脏。心房排列类型以及房室连接的形态也存在相当大的变异性。最常见的发现是通常的心房排列(n = 5)、右心耳左并列(n = 3)、房间隔缺损(n = 6)、单心室房室连接(n = 5)、室间隔缺损(n = 8)和肺动脉梗阻(n = 4)。此外,5个标本有一条冠状动脉或两条冠状动脉起源于预期的右冠状动脉主动脉窦。
心室动脉连接一致和动脉干并行可存在于多种节段组合中。通过不仅详细分析心室动脉连接,而且分析漏斗部解剖结构和动脉干的空间关系,可对这些罕见心脏做出准确诊断。需要特别关注冠状动脉。