Laparoscopic management of small bowel intussusception in a 16-year-old with Peutz-Jeghers syndrome

Angel Mario Morales Gonzalez1, Benjamin Clapp

  • 1Texas Tech University Health Sciences Center at El Paso, Department of Surgery, El Paso, Texas 79912, USA. Angel.Morales@ttuhsc.edu

Insights

Peutz-Jeghers syndrome patients experiencing bowel obstruction can be successfully treated with minimally invasive surgery. Prompt removal of the hamartomatous polyp causing the intussusception is crucial for recovery.

Area of Science:

  • Gastroenterology
  • Surgical Oncology
  • Genetics

Background:

  • Peutz-Jeghers syndrome is a rare autosomal dominant disorder.
  • Characterized by hamartomatous polyps and mucosal discoloration.
  • Polyps can cause gastrointestinal complications like bowel obstruction.

Observation:

  • A 16-year-old male with Peutz-Jeghers syndrome presented with acute bowel obstruction.
  • Symptoms included abdominal pain, obstipation, and vomiting.
  • History of colonoscopy with polypectomy and characteristic hyperpigmentation.

Findings:

  • CT scan revealed small intestine intussusception.
  • Laparoscopic surgery identified a jejunal intussusception.
  • A 5-cm polyp was the lead point; resection was performed.
  • Additional polyps found in the stomach and colon were removed.

Implications:

  • Minimally invasive approaches are effective for small bowel obstruction in Peutz-Jeghers syndrome.
  • Surgical management involves removing the causative hamartomatous polyp.
  • Comprehensive intraoperative examination and polypectomy are essential.
  • Laparoscopic-assisted enteroscopy and colonoscopy facilitate complete polyp removal.
Abstract

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