An appendiceal leiomyoma in a child with acquired immunodeficiency syndrome

Elliot Sambol1, Danielle Patterson, Rafael Rivera

  • 1Division of Pediatric Surgery, Department of Surgery, New York University School of Medicine, 530 First Avenue, Suite 10 W, New York, NY 10016, USA.

Insights

Children with acquired immunodeficiency syndrome (AIDS) face higher risks of smooth muscle tumors. This report details the first appendiceal leiomyoma case in a pediatric AIDS patient, highlighting a rare complication.

Area of Science:

  • Pediatric Oncology
  • Immunology
  • Gastroenterology

Background:

  • Children with acquired immunodeficiency syndrome (AIDS) exhibit an elevated risk for lymphoproliferative and neoplastic disorders.
  • Smooth muscle neoplasms, including leiomyomas and leiomyosarcomas, are among the potential complications.
  • The incidence of smooth muscle tumors in children with human immunodeficiency virus (HIV) infection is significantly higher than in immunocompetent children.

Observation:

  • A 12-year-old African American girl with vertically acquired AIDS presented with severe abdominal pain.
  • Abdominal exploration revealed an appendiceal leiomyoma, a previously unreported location for such a tumor in this population.
  • Lesions in HIV-infected children are typically found in the lung, liver, and gastrointestinal tract.

Findings:

  • This case represents the first documented instance of an appendiceal leiomyoma in a child with AIDS.
  • The rarity of appendiceal leiomyoma in immunocompetent children (2 per ten million) underscores the increased risk in pediatric AIDS patients.
  • The clinical presentation included severe diffuse abdominal pain, necessitating emergency evaluation.

Implications:

  • Appendiceal leiomyoma should be considered in the differential diagnosis of abdominal masses in children with AIDS.
  • This finding expands the spectrum of gastrointestinal smooth muscle neoplasms associated with pediatric HIV infection.
  • Further research is warranted to understand the pathogenesis and optimal management of these rare tumors in immunocompromised children.

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