Childhood carcinoid tumors: description of a case series in a Brazilian cancer center

Bibliographic Details
Main Author: Neves, Gustavo Ribeiro
Publication Date: 2006
Other Authors: Chapchap, Paulo, Sredni, Simone Treiger, Viana, Cristiano Ribeiro, Mendes, Wellington Luiz
Format: Article
Language: eng
Source: São Paulo medical journal (Online)
Download full: https://periodicosapm.emnuvens.com.br/spmj/article/view/2194
Summary: CONTEXT AND OBJECTIVE: Carcinoid tumors are very rare both in children and adults. About 85% of these tumors develop in the gastrointestinal tract. The objective of the present study was to describe our experience with children treated of carcinoid tumors, and investigate the frequency morphological findings and results. DESIGN AND SETTING: Report on case series, at the Department of Pediatrics of Centro de Tratamento e Pesquisa Hospital do Câncer, São Paulo. METHODS: This was a retrospective analysis of clinical pathological data and outcomes among children (< 18 years old) with carcinoid tumors admitted from January 1, 1990, to December 31, 2001. RESULTS: Nine patients (mean age 12.2 years) were included: six girls and three boys (2:1), all of them Caucasian. In eight cases (89%), the primary tumor site was the appendix and in one (11%) it was the left bronchus. For those with primary tumor in the appendix, the main complaint was abdominal pain, which led to appendectomy. Only one patient underwent right hemicolectomy due to tumor extension into the se- rosa. The patient with bronchial tumor underwent left pneumonectomy. All patients had localized disease and are alive and free of disease. They have had follow-ups lasting from 1 to 11 years (mean of 3.5 years). CONCLUSION: Although the majority of car- cinoid tumors arise from the appendix, these tumors can also occur in other primary sites. Surgical resection at an early stage allows for good prognosis without the need for any adju- vant treatment.
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spelling Childhood carcinoid tumors: description of a case series in a Brazilian cancer centerTumores carcinóides na infância: descrição de uma série de casos em um centro oncológico brasileiroTumor carcinóideTumores neuroendócrinosDiagnósticoPatologiaCirurgiaCarcinoid tumorNeuroendocrine tumorsDiagnosisPathologySurgeryCONTEXT AND OBJECTIVE: Carcinoid tumors are very rare both in children and adults. About 85% of these tumors develop in the gastrointestinal tract. The objective of the present study was to describe our experience with children treated of carcinoid tumors, and investigate the frequency morphological findings and results. DESIGN AND SETTING: Report on case series, at the Department of Pediatrics of Centro de Tratamento e Pesquisa Hospital do Câncer, São Paulo. METHODS: This was a retrospective analysis of clinical pathological data and outcomes among children (< 18 years old) with carcinoid tumors admitted from January 1, 1990, to December 31, 2001. RESULTS: Nine patients (mean age 12.2 years) were included: six girls and three boys (2:1), all of them Caucasian. In eight cases (89%), the primary tumor site was the appendix and in one (11%) it was the left bronchus. For those with primary tumor in the appendix, the main complaint was abdominal pain, which led to appendectomy. Only one patient underwent right hemicolectomy due to tumor extension into the se- rosa. The patient with bronchial tumor underwent left pneumonectomy. All patients had localized disease and are alive and free of disease. They have had follow-ups lasting from 1 to 11 years (mean of 3.5 years). CONCLUSION: Although the majority of car- cinoid tumors arise from the appendix, these tumors can also occur in other primary sites. Surgical resection at an early stage allows for good prognosis without the need for any adju- vant treatment.CONTEXTO E OBJETIVO: Tumores carcinóides são bastante raros, tanto em crianças quanto em adultos. Cerca de 85% deles desenvolvem-se no trato gastrintestinal. O objetivo do presente estudo foi descrever a experiência de nossa instituição com crianças tratadas de tumores carcinóides, investigando sua freqüência, achados morfológicos e resultados. TIPO DE ESTUDO E LOCAL: Relato de série de casos, no Departmento de Pediatria do Centro de Tratamento e Pesquisa Hospital do Câncer, São Paulo, Brasil. MÉTODOS: Análise retrospectiva de dados clinicopatológicos e resultados de crianças menores de 18 anos de idade com tumores carcinóides, admitidas entre 1o de janeiro de 1990 e 31 de dezembro de 2001. RESULTADOS: O estudo inclui nove pacientes, todos brancos, com idade média de 12,2 anos, sendo seis meninas e três meninos (2:1). O apêndice foi o sítio primário em oito casos (89%) e o brônquio esquerdo em um caso (11%). Nos primeiros, o sintoma principal foi dor abdominal que levou a apendicectomia. Apenas um paciente foi submetido a hemicolectomia direita em razão da extensão do tumor na serosa. O paciente que tinha o tumor primário no brônquio foi submetido a pneumectomia à esquerda. Todos os pacientes tinham doença localizada e estão vivos sem doença, com acompanhamento de 1 a 11 anos (média de 3,5 anos). CONCLUSÃO: Embora a maioria dos tumores carcinóides tenha sua origem no apêndice, eles podem ocorrer em outros sítios. A ressecção cirúrgica em estágios iniciais permite um bom prognóstico sem necessidade de tratamento adjuvante.São Paulo Medical JournalSão Paulo Medical Journal2006-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://periodicosapm.emnuvens.com.br/spmj/article/view/2194São Paulo Medical Journal; Vol. 124 No. 1 (2006); 21-25São Paulo Medical Journal; v. 124 n. 1 (2006); 21-251806-9460reponame:São Paulo medical journal (Online)instname:Associação Paulista de Medicinainstacron:APMenghttps://periodicosapm.emnuvens.com.br/spmj/article/view/2194/2091https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessNeves, Gustavo RibeiroChapchap, PauloSredni, Simone TreigerViana, Cristiano RibeiroMendes, Wellington Luiz2023-09-29T11:38:51Zoai:ojs.diagnosticoetratamento.emnuvens.com.br:article/2194Revistahttp://www.scielo.br/spmjPUBhttps://old.scielo.br/oai/scielo-oai.phprevistas@apm.org.br1806-94601516-3180opendoar:2023-09-29T11:38:51São Paulo medical journal (Online) - Associação Paulista de Medicinafalse
dc.title.none.fl_str_mv Childhood carcinoid tumors: description of a case series in a Brazilian cancer center
Tumores carcinóides na infância: descrição de uma série de casos em um centro oncológico brasileiro
title Childhood carcinoid tumors: description of a case series in a Brazilian cancer center
spellingShingle Childhood carcinoid tumors: description of a case series in a Brazilian cancer center
Neves, Gustavo Ribeiro
Tumor carcinóide
Tumores neuroendócrinos
Diagnóstico
Patologia
Cirurgia
Carcinoid tumor
Neuroendocrine tumors
Diagnosis
Pathology
Surgery
title_short Childhood carcinoid tumors: description of a case series in a Brazilian cancer center
title_full Childhood carcinoid tumors: description of a case series in a Brazilian cancer center
title_fullStr Childhood carcinoid tumors: description of a case series in a Brazilian cancer center
title_full_unstemmed Childhood carcinoid tumors: description of a case series in a Brazilian cancer center
title_sort Childhood carcinoid tumors: description of a case series in a Brazilian cancer center
author Neves, Gustavo Ribeiro
author_facet Neves, Gustavo Ribeiro
Chapchap, Paulo
Sredni, Simone Treiger
Viana, Cristiano Ribeiro
Mendes, Wellington Luiz
author_role author
author2 Chapchap, Paulo
Sredni, Simone Treiger
Viana, Cristiano Ribeiro
Mendes, Wellington Luiz
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Neves, Gustavo Ribeiro
Chapchap, Paulo
Sredni, Simone Treiger
Viana, Cristiano Ribeiro
Mendes, Wellington Luiz
dc.subject.por.fl_str_mv Tumor carcinóide
Tumores neuroendócrinos
Diagnóstico
Patologia
Cirurgia
Carcinoid tumor
Neuroendocrine tumors
Diagnosis
Pathology
Surgery
topic Tumor carcinóide
Tumores neuroendócrinos
Diagnóstico
Patologia
Cirurgia
Carcinoid tumor
Neuroendocrine tumors
Diagnosis
Pathology
Surgery
description CONTEXT AND OBJECTIVE: Carcinoid tumors are very rare both in children and adults. About 85% of these tumors develop in the gastrointestinal tract. The objective of the present study was to describe our experience with children treated of carcinoid tumors, and investigate the frequency morphological findings and results. DESIGN AND SETTING: Report on case series, at the Department of Pediatrics of Centro de Tratamento e Pesquisa Hospital do Câncer, São Paulo. METHODS: This was a retrospective analysis of clinical pathological data and outcomes among children (< 18 years old) with carcinoid tumors admitted from January 1, 1990, to December 31, 2001. RESULTS: Nine patients (mean age 12.2 years) were included: six girls and three boys (2:1), all of them Caucasian. In eight cases (89%), the primary tumor site was the appendix and in one (11%) it was the left bronchus. For those with primary tumor in the appendix, the main complaint was abdominal pain, which led to appendectomy. Only one patient underwent right hemicolectomy due to tumor extension into the se- rosa. The patient with bronchial tumor underwent left pneumonectomy. All patients had localized disease and are alive and free of disease. They have had follow-ups lasting from 1 to 11 years (mean of 3.5 years). CONCLUSION: Although the majority of car- cinoid tumors arise from the appendix, these tumors can also occur in other primary sites. Surgical resection at an early stage allows for good prognosis without the need for any adju- vant treatment.
publishDate 2006
dc.date.none.fl_str_mv 2006-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://periodicosapm.emnuvens.com.br/spmj/article/view/2194
url https://periodicosapm.emnuvens.com.br/spmj/article/view/2194
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://periodicosapm.emnuvens.com.br/spmj/article/view/2194/2091
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv São Paulo Medical Journal
São Paulo Medical Journal
publisher.none.fl_str_mv São Paulo Medical Journal
São Paulo Medical Journal
dc.source.none.fl_str_mv São Paulo Medical Journal; Vol. 124 No. 1 (2006); 21-25
São Paulo Medical Journal; v. 124 n. 1 (2006); 21-25
1806-9460
reponame:São Paulo medical journal (Online)
instname:Associação Paulista de Medicina
instacron:APM
instname_str Associação Paulista de Medicina
instacron_str APM
institution APM
reponame_str São Paulo medical journal (Online)
collection São Paulo medical journal (Online)
repository.name.fl_str_mv São Paulo medical journal (Online) - Associação Paulista de Medicina
repository.mail.fl_str_mv revistas@apm.org.br
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