Nagae Itsuro, Tsuchida Akihiko, Tanabe Yoshihide, Takahashi Soshi, Minato Shintaro, Aoki Tatsuya
Third Department of Surgery, Tokyo Medical University, Tokyo 160-0023, Japan.
J Pediatr Surg. 2005 Oct;40(10):e11-3. doi: 10.1016/j.jpedsurg.2005.06.030.
Gross E-type congenital esophageal atresia associated with congenital esophageal stenosis is extremely rare. In a male infant born at 36 weeks of gestation, bubbly vomiting was noted after birth. X-ray films of the chest and abdomen showed coil-up sign of the nasogastric tube and gas in the stomach and small intestines were recognized, so gross C-type esophageal atresia was suspected and surgery was performed on the first day of life. Surgery revealed the presence of a tracheoesophageal fistula in the upper esophagus and membranous stenosis on the distal side.
伴有先天性食管狭窄的粗大E型先天性食管闭锁极为罕见。在一名妊娠36周出生的男婴中,出生后即发现有泡沫样呕吐。胸部和腹部X线片显示鼻胃管呈盘曲状,胃和小肠内有气体,因此怀疑为粗大C型食管闭锁,并在出生第一天进行了手术。手术发现上段食管存在气管食管瘘,下段有膜性狭窄。