一例罕见的宫内肠套叠、回肠闭锁和复杂胎粪回流病例:病例报告

Q4 Medicine
Jonathan Hencke, O. Diez, Steffan Loff
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引用次数: 0

摘要

背景:宫内肠套叠虽然非常罕见(<2%),但却是导致肠闭锁的潜在原因之一。它通常在婴儿出生后数小时或数天内表现为肠梗阻:我们报告了一例因胎儿腹水而导致早期剖宫产的病例,随后进行了经皮腹腔引流和开腹手术。术中发现胎粪腹膜炎和 IIIa 型回肠闭锁,远端有肠套叠,坏死的肠套叠可能导致穿孔和回肠闭锁;此外,远端回肠有胎粪回流的迹象。在建立回肠造口术后,术后恢复顺利。通过出汗试验排除了囊性纤维化:结论:新生儿肠梗阻继发于胎儿腹水、肠套叠、复杂性胎粪回肠症和回肠闭锁的不寻常组合,及时诊断和处理可获得良好的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A remarkable case of intrauterine intussusception, ileal atresia, and complicated meconium ileus: A case report
Background: Intrauterine intussusception, although very rare (<2%), is a potential cause of intestinal atresia. It usually manifests as bowel obstruction during the first hours or days of life. Case Presentation: We report a case with fetal ascites prompting early Cesarean section, with subsequent percutaneous abdominal drainage and laparotomy. Intraoperative findings showed meconium peritonitis and type IIIa ileal atresia with intussusception of the distal part, with the necrosed intussusceptum likely causing perforation and ileal atresia; in addition, the distal ileum demonstrated signs of meconium ileus. After ileostomy creation, the postoperative course was uneventful. Cystic fibrosis was excluded via a sweat test. Conclusion: Prompt diagnosis and management of neonatal intestinal obstruction secondary to the unusual combination of fetal ascites, intussusception, complicated meconium ileus, and ileal atresia results in a favorable outcome.
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来源期刊
Journal of Neonatal Surgery
Journal of Neonatal Surgery Medicine-Surgery
CiteScore
0.30
自引率
0.00%
发文量
29
审稿时长
6 weeks
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