Despite the increasing incidence of gastroschisis, the cause remains unknown. Genetic factors may contribute to bowel anomalies as demonstrated by cases of gastroschisis in twins and siblings, and other types of bowel anomalies in twins. Atresia of the colon represents one of the rarest causes of neonatal intestinal obstruction. We present the first case of dichorionic, diamniotic male twins in which there was gastroschisis with jejunal and colonic atresia in Twin A and isolated colonic atresia in Twin B.
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http://dx.doi.org/10.1007/s00383-009-2353-7 | DOI Listing |
JPGN Rep
November 2024
Department of Pediatrics, Division of Gastroenterology, Center of Excellence in Thai Pediatric Gastroenterology, Hepatology and Immunology (TPGHAI), King Chulalongkorn Memorial Hospital, The Thai Red Cross Society, Faculty of Medicine Chulalongkorn University Bangkok Thailand.
Acquired colonic stenosis is extremely rare in infants and surgical resection is the mainstay of treatment. Endoscopic balloon dilation has shown success in treating bowel stenosis from inflammatory bowel disease but its application in infants with colonic strictures of other origin has not been widely explored. We report a 4-week-old male infant who developed significant abdominal distension due to progressive colonic stenosis, occurring 2 weeks following balloon valvuloplasty for his severe valvular pulmonary stenosis.
View Article and Find Full Text PDFJ Pediatr Surg
September 2024
Rady Children's Hospital San Diego, Division of Pediatric Surgery, 3020 Children's Way, San Diego, CA 92123, USA; UCSD School of Medicine, Department of Surgery, 9500 Gilman Dr, La Jolla, CA 92093, USA. Electronic address:
Int J Surg Case Rep
October 2024
Department of Surgery, University of Kansas Medical Center, Kansas City, KS 66103, USA.
J Surg Case Rep
August 2024
Department of Paediatric Surgery and Urology, Southampton Children's Hospital, Southampton SO16 6YD, United Kingdom.
We describe cases of three infants who developed acquired colonic atresia presumed secondary to significant systemic cardiovascular compromise and in the absence of necrotizing enterocolitis. An acquired colonic atresia may present as feed intolerance and should be investigated with a lower gastrointestinal contrast study. We would also recommend routine lower gastrointestinal contrast study prior to stoma closure in an infant with history of significant cardiovascular compromise, even in the absence of significant widespread colonic inflammation such as necrotizing enterocolitis.
View Article and Find Full Text PDFJ Pediatr Surg
November 2024
Section of Pediatric Surgery, Pediatric Liver and Gut Research Group, Pediatric Research Center, Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Aim Of The Study: We aimed to evaluate disease characteristics, associated malformations and surgical outcomes of congenital intestinal atresia.
Methods: We identified all patients with jejunoileal (JIA) or colonic atresia (CA) treated at the Helsinki University Children's hospital during 1947-2019 and collected clinical data retrospectively from archived and electronic medical records.
Results: Of the 180 included patients, 156 had JIA and 24 CA.
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