Xiong Shiqiu, Ge Kuku, Hou Chongzhi, Yang Hongbin, Zhang Hanhua, Zhang Sheng, Liu Bailing, Hao Yuewen, Fang Ying, Ren Xiaoxia
Department of Gastroenterology, Xi'an Children's Hospital, The Affiliated Children's Hospital of Xi'an Jiaotong University, Xi 'an, Shaanxi, China.
Department of General Surgery, Xi'an Children's Hospital, The Affiliated Children's Hospital of Xi'an Jiaotong University, Xi 'an, Shaanxi, China.
Front Pediatr. 2025 Jan 17;13:1491520. doi: 10.3389/fped.2025.1491520. eCollection 2025.
Anomalous congenital bands are a rare cause of intestinal obstruction, with only five previously reported cases involving duodenal obstruction. We present a fifth case of duodenal obstruction due to two congenital bands and provide a comprehensive literature review summarizing the clinical features of this condition.
An eight-year-old girl was admitted to our department with recurrent bilious vomiting and abdominal pain lasting six days. She had no significant past medical history, with no previous abdominal surgeries or trauma. Physical examination revealed abdominal tenderness and decreased bowel sounds. Contrast x-ray showed an obstructed passage of contrast through the third part of the duodenum. Abdominal ultrasound identified a strip-like hypoechoic structure compressing the third part of the duodenum. A diagnosis of duodenal obstruction was confirmed, and laparoscopic surgery combined with gastroduodenoscopy was performed. The procedure revealed two congenital bands adjacent to the duodenum: one extending from the duodenum to the transverse colon, and the other from the duodenum to the root of the mesentery. The bands were resected, and gastroduodenoscopy confirmed the resolution of the obstruction.
We reviewed 93 cases of anomalous congenital bands, including the present one, comprising 33 adults and 60 children, with 71.0% of the cases involving males. Common symptoms included vomiting and abdominal pain, with physical examinations often showing tenderness and distension. Imaging techniques like plain x-ray, contrast x-ray, ultrasound, and computed tomography often indicated intestinal obstruction but were less effective in directly identifying congenital bands. All cases required abdominal surgery for diagnosis and treatment. Congenital bands were primarily found attached to the ileum or its mesentery and were resected in all cases, with a favorable postoperative prognosis. This case and the literature review provide valuable insights for clinical diagnosis and treatment.
先天性异常束带是肠梗阻的罕见病因,此前仅有5例涉及十二指肠梗阻的报道。我们报告了因两条先天性束带导致十二指肠梗阻的第5例病例,并提供了一篇全面的文献综述,总结了该病症的临床特征。
一名8岁女孩因反复胆汁性呕吐和腹痛6天入院。她既往无重大病史,未接受过腹部手术或外伤。体格检查发现腹部压痛,肠鸣音减弱。造影X线显示造影剂通过十二指肠第三段受阻。腹部超声发现一条带状低回声结构压迫十二指肠第三段。确诊为十二指肠梗阻后,进行了腹腔镜手术联合胃十二指肠镜检查。手术发现两条与十二指肠相邻的先天性束带:一条从十二指肠延伸至横结肠,另一条从十二指肠延伸至肠系膜根部。切除束带后,胃十二指肠镜检查证实梗阻已解除。
我们回顾了93例先天性异常束带病例,包括本病例,其中成人33例,儿童60例,71.0%的病例为男性。常见症状包括呕吐和腹痛,体格检查常显示压痛和腹胀。普通X线、造影X线、超声和计算机断层扫描等影像学技术常提示肠梗阻,但在直接识别先天性束带方面效果较差。所有病例均需进行腹部手术以明确诊断和治疗。先天性束带主要附着于回肠或其肠系膜,所有病例均进行了切除,术后预后良好。本病例及文献综述为临床诊断和治疗提供了有价值的见解。