A rare lipoma site in a 1-year-old boy

Gulan Maree1, Bardisan Gawrieh1, Ammar Omran1

  • 1Pediatric Surgery Department, Tishreen University Hospital, Lattakia, Syria.

Insights

This case report details an extremely rare instance of a mesenteric lipoma in a 1-year-old child. The benign fatty tumor was successfully removed, highlighting the importance of investigating abdominal masses in pediatric patients.

Area of Science:

  • Pediatric Surgery
  • Surgical Pathology
  • Gastrointestinal Oncology

Background:

  • Lipomas, benign tumors of mature adipocytes, are uncommon in the pediatric gastrointestinal tract.
  • Mesenteric lipomas are particularly rare, with limited case reports in the literature.
  • Early detection and surgical management are crucial for pediatric abdominal masses.

Observation:

  • A 1-year-old male presented with abdominal distention and chronic diarrhea.
  • An abdominal mass was incidentally detected during a routine pediatric examination.
  • Imaging studies, including ultrasound and CT scan, identified a significant fat-containing mass.

Findings:

  • Laparotomy revealed a soft, yellow mass attached to the jejunal mesentery.
  • Histopathological examination confirmed the diagnosis of a lipoma.
  • The mass was successfully enucleated without the need for bowel anastomosis.

Implications:

  • This case underscores the rarity of mesenteric lipomas in infants, emphasizing the need for vigilance in diagnosing pediatric abdominal masses.
  • Complete surgical excision is an effective treatment for pediatric mesenteric lipomas.
  • Postoperative follow-up confirmed successful recovery, highlighting the importance of multidisciplinary care.

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