Chen Bang-Bin, Hsieh Hong-Jen, Chiu Ing-Sh, Chen Shyh-Jye, Wu Mei-Hwan
Department of Medical Imaging, National Taiwan University Hospital, Taipei, Taiwan.
J Formos Med Assoc. 2008 Mar;107(3):265-9. doi: 10.1016/S0929-6646(08)60146-1.
Crossed pulmonary arteries are due to an anomalous origin of both pulmonary arteries from the main pulmonary trunk. This anatomy is often associated with other congenital cardiac and extracardiac diseases. We report two neonates with complex congenital heart disease who had this disorder, which was detected during cardiac computed tomography (CT) with three-dimensional reconstruction but not during echocardiography or angiography. The first patient was a 3-day-old male neonate who had tachypnea and feeding problems since birth. Cardiac CT showed crossed pulmonary arteries, type B interruption of the aortic arch, a ventricular septal defect, and a large patent ductus arteriosus. He received an emergency T-colostomy at 3 days of age because of severe bowel distention. Low-type imperforated anus was diagnosed. His postoperative course was complicated with fluctuated saturation, seizure, hypocalcemia, hyperphosphatemia, and sepsis. Also found were cardiac defects, abnormal facies, thymic hypoplasia, cleft palate, hypocalcemia, and a variable deletion on chromosome 22q11 (CATCH 22 disorder). Because of his poor prognosis, the patient was transferred to another hospital on day 16 for further care, at the family's request. The other patient was a 5-day-old female neonate who had a heart murmur since birth. Cardiac CT showed crossed pulmonary arteries, truncus arteriosus, type A interruption of the aortic arch, a ventricular septal defect, an atrial septal defect, and a large patent ductus arteriosus. She received complete surgical correction, including division of the patent ductus arteriosus and repair of the other defects. Intermittent respiratory distress and decreased blood pressure complicated her postoperative course, and she died on the eighth day after surgery. Crossed pulmonary arteries complicated accurate interpretation of two-dimensional echocardiographs of the great vessels, as well as the course and location of catheters during cardiac catheterization. Three-dimensional CT provided a noninvasive approach to clearly recognize these malformations and the related anatomic structures. This information is important in planning and performing surgery in neonates with crossed pulmonary arteries.
交叉肺动脉是指肺动脉均起源于主肺动脉干的异常情况。这种解剖结构常与其他先天性心脏和心外疾病相关。我们报告了两名患有复杂先天性心脏病且伴有交叉肺动脉的新生儿,该病症是在心脏计算机断层扫描(CT)三维重建时被发现的,而在超声心动图或血管造影检查中未被检测到。第一名患者是一名3日龄男婴,自出生以来就有呼吸急促和喂养困难的症状。心脏CT显示有交叉肺动脉、B型主动脉弓中断、室间隔缺损和大型动脉导管未闭。由于严重的肠扩张,他在3日龄时接受了紧急T形结肠造口术。诊断为低位型肛门闭锁。他术后出现了饱和度波动、癫痫发作、低钙血症、高磷血症和败血症等并发症。还发现了心脏缺陷、面容异常、胸腺发育不全、腭裂、低钙血症以及22q11染色体可变缺失(22q11缺失综合征)。由于预后不佳,应家属要求,该患者在第16天被转至另一家医院接受进一步治疗。另一名患者是一名5日龄女婴,自出生以来就有心脏杂音。心脏CT显示有交叉肺动脉、动脉干、A型主动脉弓中断、室间隔缺损、房间隔缺损和大型动脉导管未闭。她接受了包括动脉导管未闭分离和其他缺损修复在内的完全手术矫正。术后她出现了间歇性呼吸窘迫和血压下降等并发症,并在术后第八天死亡。交叉肺动脉使对大血管二维超声心动图的准确解读以及心脏导管插入术期间导管的行程和位置变得复杂。三维CT提供了一种非侵入性方法,可清晰识别这些畸形及相关解剖结构。这些信息对于计划和实施患有交叉肺动脉的新生儿手术非常重要。