Elrouby Ahmed, Koraitim Ahmed
Department of Pediatric Surgery, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
European J Pediatr Surg Rep. 2020 Jan;8(1):e7-e9. doi: 10.1055/s-0039-3400488. Epub 2020 Feb 7.
Multiple point duodenal atresia is an extremely rare condition with atretic segments in either two or three sites of the duodenum. We report a newborn male patient who presented to our institution with bilious vomiting, nonpassage of meconium, mild abdominal distension, and a palpable epigastric abdominal mass ∼1 × 1 cm. A faint double bubble was found on abdominal X-ray. On exploratory laparotomy, a duodenal cyst due to double duodenal atresia was found and a typical diamond-shaped duodeno-duodenostomy was created. A postoperative contrast study revealed passage of the contrast media into distal intestine. However, the patient died 2 weeks later due to uncontrolled sepsis and pneumonia. Despite the fact that multiple-point duodenal atresia is a rare condition, it should be considered as a differential diagnosis to avoid missed pathology.
多点十二指肠闭锁是一种极其罕见的疾病,十二指肠的两个或三个部位存在闭锁段。我们报告了一名新生儿男性患者,他因胆汁性呕吐、胎粪未排出、轻度腹胀以及可触及约1×1厘米的上腹部肿块而就诊于我院。腹部X线检查发现一个模糊的双泡征。在剖腹探查术中,发现了因双十二指肠闭锁导致的十二指肠囊肿,并进行了典型的菱形十二指肠-十二指肠吻合术。术后造影检查显示造影剂进入远端肠道。然而,患者在2周后因败血症和肺炎控制不佳而死亡。尽管多点十二指肠闭锁是一种罕见疾病,但仍应将其作为鉴别诊断考虑,以避免漏诊病变。