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Symptomatic omphalomesenteric duct anomalies in children. | LitMetric

Symptomatic omphalomesenteric duct anomalies in children.

S Afr J Surg

Department of Paediatric Surgery, Mehmet Akif İnan Training and Research Hospital, Turkey.

Published: October 2024

AI Article Synopsis

  • The study focused on children with symptomatic omphalomesenteric duct (OMD) anomalies, analyzing 35 cases from a hospital over four years.
  • Most patients were male (82.8%) with symptoms primarily related to gastrointestinal tract obstruction, acute abdomen, or umbilical issues.
  • Surgical interventions varied, with successful outcomes and only two complications, showcasing the effectiveness of surgical treatment for these anomalies.

Article Abstract

Background: We aimed to present our experience with children with symptomatic omphalomesenteric duct (OMD) anomalies and evaluate the patients' characteristics, treatment, and outcomes.

Methods: Records of children who were operated for symptomatic OMD anomalies in Şanlıurfa Training and Research Hospital between October 2018 and November 2022 were retrospectively analysed.

Results: There were 35 patients with a median age of 31.7 (1 day-17 years) weeks, 29 (82.8%) males and six (17.2%) females. The presenting signs were gastrointestinal tract (GIT) obstruction in 17 (48.6%) patients, acute abdomen in 11 (31.4%), umbilical abnormalities in four (11.4%) and rectal bleeding in three (8.6%). All patients presenting with umbilical abnormalities were newborn. These were OMD fistula to skin ( = 1), OMD fistula to umbilical cord hernia sac ( = 1), OMD cyst in umbilical cord hernia ( = 1) and OMD band adherence to umbilical cord hernia sac ( = 1). Meckel's scan was positive in all three patients with rectal bleeding. Surgical findings in patients other than umbilical abnormalities were diverticulitis (with/without perforation) ( = 14), intussusception due to diverticulum ( = 9) and Meckel's band obstruction ( = 8). At surgery, an ileal resection was performed in 19 cases, wedge resection in 10 cases, resection with stapler in five cases and ileocolonic resection in one patient. On histopathological examination, ectopic gastric mucosa was detected in 11 specimens and both gastric and pancreatic tissue in two. There were only two cases of postoperative complications (incisional hernia, = 1, postoperative colon perforation due to forced manual reduction of intussusception, = 1) and all patients survived in good condition.

Conclusion: In the present study, GIT obstruction is the primary symptom in patients with symptomatic OMD anomalies, with umbilical anomalies exclusively found in newborns. Surgery is confirmed as the definitive treatment, with wedge resection and simple diverticulectomy being safe but sometimes insufficient. A significant portion of patients might need more complex segmental bowel resections due to severe complications. With ectopic tissue found in about one-third of cases, managing OMD anomalies presents distinct challenges.

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