Beasley S W, Allen M, Myers N
Department of Paediatric Surgery, Christchurch Hospital, Private Bag 4710, Christchurch, New Zealand.
Pediatr Surg Int. 1997;12(8):550-1. doi: 10.1007/BF01371897.
Recognisable chromosomal abnormalities occur in over 5% of patients with oesophageal atresia (OA). In a review of 670 patients with OA chromosomal abnormalities were identified in 35 (5.2%), of whom 16 had trisomy 18 and 12 had trisomy 21. In patients with trisomy 18, the diagnosis should be suspected on clinical grounds and confirmed on analysis of chromosomes; no active treatment of the OA is justified because of the extremely poor prognosis. In Down syndrome (DS) 50% will have pure OA with no tracheo-oesophageal fistula. In addition, many of these infants will have associated anomalies typical of those normally seen in DS, eg., Hirschsprung's disease, duodenal atresia, and congenital heart disease. Despite treatment, OA with DS has a high mortality.
超过5%的食管闭锁(OA)患者存在可识别的染色体异常。在一项对670例OA患者的回顾性研究中,发现35例(5.2%)存在染色体异常,其中16例为18三体,12例为21三体。对于18三体患者,应根据临床情况怀疑诊断,并通过染色体分析加以证实;由于预后极差,对OA进行积极治疗并无道理。在唐氏综合征(DS)患者中,50%会出现单纯性OA且无气管食管瘘。此外,许多此类婴儿还会伴有DS患者常见的典型相关畸形,例如先天性巨结肠、十二指肠闭锁和先天性心脏病。尽管进行了治疗,DS合并OA的死亡率仍很高。