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A half century of experience with carcinoid tumors in children.
Corpron, C A; Black, C T; Herzog, C E; Sellin, R V; Lally, K P; Andrassy, R J.
  • Corpron CA; Department of Surgical Oncology, University of Texas M.D., Anderson Cancer Center, Houston, USA.
Am J Surg ; 170(6): 606-8, 1995 Dec.
Article en En | MEDLINE | ID: mdl-7492010
ABSTRACT

PURPOSE:

To investigate the frequency, presentation, clinical management, and prognosis of appendiceal carcinoid tumors in children.

METHOD:

A review of our institution's experience over 50 years.

RESULTS:

Twenty-two patients below the age of 20 presented with appendiceal carcinoid tumor. The mean age at presentation was 14.6 years. Twelve patients presented with symptoms of appendicitis. No tumor was > 2.0 cm in size. Only 2 patients underwent resection beyond appendectomy. No patient had recurrent or metastatic carcinoid tumor, and all but 1 patient (who died of ovarian choriocarcinoma) are alive without evidence of carcinoid tumors 1.5 to 30 years after diagnosis.

CONCLUSIONS:

Appendiceal carcinoid tumors in children are rarely life-threatening and the incidence of large tumors (> 2.0 cm) is very low. The role of right hemicolectomy in large (> 2.0 cm) tumors is questionable in this age group.
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Banco de datos: MEDLINE Asunto principal: Neoplasias del Apéndice / Tumor Carcinoide Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Año: 1995 Tipo del documento: Article
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Banco de datos: MEDLINE Asunto principal: Neoplasias del Apéndice / Tumor Carcinoide Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Año: 1995 Tipo del documento: Article