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[Appendicular carcinoid tumor in childhood].

F Vázquez Rueda1, J L Valdivieso García, J Salas Molina

  • 1Servicio de Cirugía Pediátrica, Hospital Universitario Reina Sofía, Córdoba.

Cirugia Pediatrica : Organo Oficial De La Sociedad Espanola De Cirugia Pediatrica
|October 1, 1992
PubMed
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Appendiceal carcinoid tumors are rare, found in less than 0.1% of appendectomies. This case highlights a 13-year-old diagnosed with appendicitis, whose appendix revealed a 6mm carcinoid tumor, successfully treated with non-invasive methods and showing no recurrence after two years.

Area of Science:

  • Gastroenterology
  • Surgical Pathology

Background:

  • Appendiceal carcinoid tumors are rare neoplasms, accounting for less than 0.1% of appendectomies.
  • Early diagnosis and appropriate management are crucial for favorable outcomes.

Observation:

  • A 13-year-old female presented with symptoms of acute appendicitis.
  • Surgical removal of the appendix was performed.
  • Histopathological examination confirmed a 6 mm appendiceal carcinoid tumor.

Findings:

  • The resected appendix contained a 6 mm carcinoid tumor.
  • A non-invasive treatment approach was selected for the patient.
  • Two-year follow-up revealed no evidence of tumor recurrence.

Implications:

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  • This case underscores the importance of histological examination of appendectomies, even in cases of acute appendicitis.
  • Non-invasive treatment may be a viable option for select cases of small appendiceal carcinoid tumors.
  • Long-term surveillance is essential to ensure the absence of recurrence.