{"title":"Anomalous congenital bands associated with necrotizing enterocolitis in a term neonate: A case report","authors":"Amr Khalil , Natashia Seemann , Orlando da Silva","doi":"10.1016/j.epsc.2024.102839","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>We report a rare occurrence in which a term infant with intestinal anomalous congenital bands (ACB), presented with bloody stools and necrotizing enterocolitis (NEC), instead of the typical intestinal obstruction picture. Our case differs from the reported cases of ACB in its presentation as bloody stools and necrotizing enterocolitis, rather than the classic symptoms of intestinal obstruction (IO).</p></div><div><h3>Case presentation</h3><p>A term neonate who was admitted to the Neonatal Intensive Care Unit (NICU) because of hypoglycemia, developed bloody stools and a clinical picture of NEC. She was treated by antibiotics and kept NPO for 7 days during which her symptoms resolved. Upon refeeding and after reaching full feeding volumes, her bloody stools recurred which warranted expanding the differential diagnosis and further investigations including lower gastrointestinal (GI) contrast study. The lower GI contrast study showed multiple filling defects indicating GI obstruction. Laparotomy was performed to explore and release the cause of obstruction. Laparotomy revealed Anomalous Congenital Bands (ACB) in the colon and cecum causing almost complete obstruction of the intestinal lumen. The ACB were excised, and the stricture segments of bowel were resected, and primary anastomosis was completed. Feeding was resumed with no recurrence of symptoms.</p></div><div><h3>Conclusion</h3><p>Anomalous congenital bands may present with bloody stools and clinical picture of NEC rather that the classic presentation of intestinal obstruction.</p></div>","PeriodicalId":45641,"journal":{"name":"Journal of Pediatric Surgery Case Reports","volume":"108 ","pages":"Article 102839"},"PeriodicalIF":0.2000,"publicationDate":"2024-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2213576624000678/pdfft?md5=dbbc4d127293d94cda0f21a60796308d&pid=1-s2.0-S2213576624000678-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pediatric Surgery Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2213576624000678","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction
We report a rare occurrence in which a term infant with intestinal anomalous congenital bands (ACB), presented with bloody stools and necrotizing enterocolitis (NEC), instead of the typical intestinal obstruction picture. Our case differs from the reported cases of ACB in its presentation as bloody stools and necrotizing enterocolitis, rather than the classic symptoms of intestinal obstruction (IO).
Case presentation
A term neonate who was admitted to the Neonatal Intensive Care Unit (NICU) because of hypoglycemia, developed bloody stools and a clinical picture of NEC. She was treated by antibiotics and kept NPO for 7 days during which her symptoms resolved. Upon refeeding and after reaching full feeding volumes, her bloody stools recurred which warranted expanding the differential diagnosis and further investigations including lower gastrointestinal (GI) contrast study. The lower GI contrast study showed multiple filling defects indicating GI obstruction. Laparotomy was performed to explore and release the cause of obstruction. Laparotomy revealed Anomalous Congenital Bands (ACB) in the colon and cecum causing almost complete obstruction of the intestinal lumen. The ACB were excised, and the stricture segments of bowel were resected, and primary anastomosis was completed. Feeding was resumed with no recurrence of symptoms.
Conclusion
Anomalous congenital bands may present with bloody stools and clinical picture of NEC rather that the classic presentation of intestinal obstruction.
导言:我们报告了一例罕见病例,一名患有先天性肠道异常带(ACB)的足月新生儿出现血便和坏死性小肠结肠炎(NEC),而不是典型的肠梗阻症状。我们的病例与已报道的先天性肠道畸形带病例不同,它表现为血便和坏死性小肠结肠炎,而不是典型的肠梗阻(IO)症状。她接受了抗生素治疗,并在 7 天内保持无呕吐,在此期间她的症状有所缓解。在重新喂养并达到全量喂养后,她的血便再次出现,因此需要扩大鉴别诊断范围并进行进一步检查,包括下消化道造影检查。下消化道造影检查显示多处充盈缺损,表明存在消化道梗阻。为探明并解除梗阻原因,对她进行了腹腔手术。腹腔手术发现结肠和盲肠内有先天性异常带(ACB),几乎完全阻塞了肠腔。切除了先天性异常带,切除了狭窄的肠段,并完成了初次吻合术。结论:异常的先天性肠带可能表现为血便和 NEC 临床表现,而不是典型的肠梗阻表现。