Ravi Patcharu, Jaiprakash Yadav, K. Chand, Badal Parikh
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引用次数: 0
摘要
背景:消化道重复是一种罕见的先天性畸形,其中真正的幽门重复仅占2.2%。它们表现为非胆汁性呕吐和类似肥厚性幽门狭窄(HPS)。腔内幽门重复在剖腹手术中不能单独看到,这使其诊断变得困难。病例介绍:我们的病例是一名新生儿,患有腔内幽门重复囊肿,并伴有反复呕吐。放射学评估显示,十二指肠第二部分内侧有一个朝向胃小曲的重复囊肿,具有胃出口梗阻的特征。术中,在打开幽门时发现管腔内1 x 2 cm的囊性肿块,将其切除并进行幽门成形术。术后婴儿出院,情况稳定。结论:腔内幽门重复囊肿是罕见的,临床表现类似HPS。对于以胃出口梗阻为特征的新生儿,应将其视为鉴别诊断。
Intraluminal pyloric duplication cyst- a rare cause of non-bilious vomiting in a neonate: A case report
Background: Duplications of the alimentary tract are rare congenital malformations, out of which, true pyloric duplications constitute only 2.2%. They present with non-bilious vomiting and mimic hypertrophic pyloric stenosis (HPS). Pyloric duplications that are intraluminal are not separately visible at laparotomy, making their diagnosis difficult.
Case presentation: Our case is a neonate with an intraluminal pyloric duplication cyst who presented with recurrent vomiting. The radiological evaluation suggested a duplication cyst medial to the second part of the duodenum towards the stomach’s lesser curvature with features of gastric outlet obstruction. Intraoperatively, a cystic mass of 1 x 2 cm intraluminally was found on opening the pylorus which was excised and pyloroplasty was done. Postoperatively the baby was discharged in a stable condition.
Conclusion: Intraluminal pyloric duplication cysts are rare and the clinical presentation mimics HPS. They should be considered as a differential diagnosis in a neonate presenting with features of gastric outlet obstruction.