ArticleCureus2025
Perforated Meckel's Diverticulum in an Infant: A Case Report and Review of the Literature.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Meckel's diverticulum (MD) is the most common congenital malformation of the gastrointestinal tract, but perforation of this diverticulum is a rare complication, especially in infants. Diagnosing this complication before surgery can be difficult, and it is typically confirmed through laparotomy. This report describes an eight-month-old female infant who was brought to the emergency department with a history of persistent crying, fever, vomiting, and one occurrence of currant jelly stool in the past 12 hours. A physical examination revealed abdominal distension, tenderness, and rigidity. An abdominal ultrasound indicated free intra-abdominal fluid containing micro-echoic elements. An exploratory laparotomy was performed, during which pus was found in the abdominal cavity. A perforated MD was identified, located 60 cm proximal to the ileocecal valve. An enterectomy and end-to-end anastomosis were performed to remove the perforated diverticulum. The postoperative course was uneventful, and the infant was discharged on the eighth postoperative day. Histopathological examination confirmed the presence of a perforated MD with ectopic gastric mucosa. This report summarizes and characterizes the presentation, diagnosis, and management of this rare complication.
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