Appendix carcinoids in childhood: long-term experience at a single institution in Western Canada and systematic

Ketan P Kulkarni1, Consolato Sergi

  • 1Department of Pediatric Oncology, Stollery Children's Hospital, University of Alberta Hospital, Edmonton, Alberta, Canada.

Insights

Pediatric appendix carcinoids (AC) are best managed with early surgical resection, leading to excellent outcomes. Genetic counseling may be beneficial due to potential links with colon cancer.

Area of Science:

  • Pediatric Oncology
  • Surgical Pathology
  • Gastrointestinal Oncology

Background:

  • Appendix carcinoids (AC) are rare neuroendocrine tumors.
  • Management strategies for pediatric AC require further elucidation.

Purpose of the Study:

  • To describe the management experience of children diagnosed with appendix carcinoids.
  • To compare institutional data with existing literature on pediatric AC.

Main Methods:

  • Systematic literature review of PubMed, EMBASE, and SCOPUS databases.
  • Inclusion of data from Stollery Children's Hospital (2000-2010).
  • Analysis of 206 identified studies on pediatric AC.

Main Results:

  • Seven pediatric patients with AC were identified (mean age 15 years; 3:4 male:female ratio).
  • Five patients presented with acute appendicitis; tumors averaged 1.4 cm.
  • No distant metastases were observed; all patients had excellent outcomes post-surgery.

Conclusions:

  • Older age at diagnosis, female predominance, and small tumor size (<1.5 cm) characterize pediatric AC.
  • Early surgical resection offers an excellent prognosis for pediatric appendix carcinoids.
  • Genetic counseling is recommended due to potential association with familial adenomatous polyposis and colonic adenocarcinoma.
Abstract

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