Jan Iftikhar Ahmad, Al Nuaimi Asma, Al Hamoudi Basma, Al Naqbi Khalid, Bilal Mohammad
Department of Pediatric Surgery, Zayed Military Hospital, Abu Dhabi, UAE.
Department of Pediatrics, Zayed Military Hospital, Abu Dhabi, UAE.
J Coll Physicians Surg Pak. 2016 Feb;26(2):148-50.
Esophageal duplication cysts are rare congenital abnormalities of the foregut and may be associated with other conditions. Association of esophageal duplication with Gastro-Esophageal Reflux Disease (GERD) has not been reported in children. We are reporting a case of a 16 months baby who had antenatal diagnosis of diaphragmatic hernia. Postnatal CTchest, however, suggested a distal esophageal duplication cyst and a contrast esophagogram showed grade-IV GER. A thoracoscopy in another hospital excluded esophageal duplication at that time. Later, he presented with hematemesis in our department and was re-evaluated. Repeat CTconfirmed a persistent 2.5 x 1.3 cm cyst in distal esophagus. Upper GI endoscopy suggested grade-II esophagitis with a wide patent gastro-esophageal junction. The child was treated with left thoracotomy, excision of the duplication cyst and thoracic fundoplication. He had an uneventful post-operative recovery and is doing well at 6 months follow-up.
食管重复囊肿是一种罕见的前肠先天性异常,可能与其他病症相关。儿童食管重复与胃食管反流病(GERD)的关联尚未见报道。我们报告一例16个月大的婴儿,产前诊断为膈疝。然而,产后胸部CT提示远端食管重复囊肿,食管造影显示IV级GER。当时在另一家医院进行的胸腔镜检查排除了食管重复。后来,他在我们科室出现呕血并接受重新评估。重复CT证实远端食管有一个持续存在的2.5×1.3 cm囊肿。上消化道内镜检查提示II级食管炎,胃食管交界处宽阔且通畅。该患儿接受了左胸切开术、重复囊肿切除术和胸段胃底折叠术。术后恢复顺利,随访6个月情况良好。