先天性食管闭锁是极其严重的消化道畸形。欧美国家发生率甚高,据 Shaw 氏统计,其发生率为出生婴儿的1/3000。国内报导很少,仅见石美鑫氏及余亚雄氏二篇。我院自1957年到1973年之间,共收容7例先天性食管闭锁病人,按照 Gross 分类法,其中5例属 C 型,1例属 A 型。兹将此6例先天性食管闭锁病人的情况,结合文献复习,报告如下。病例报告 Congenital esophageal atresia is extremely serious gastrointestinal malformations. The incidence of Europe and the United States is very high, according to Shaw’s statistics, the incidence of birth of 1/3 000. Few domestic reports, only to see Shi Meixin and Yu Yaxiong two. In our hospital from 1957 to 1973, a total of 7 patients with congenital esophageal atresia were admitted. According to the Gross classification, 5 were C-type and 1 was A-type. The 6 cases of congenital esophageal atresia patients, combined with the literature review, the report is as follows. Case Reports