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

Detalhes bibliográficos
Autor(a) principal: Neves,Gustavo Ribeiro
Data de Publicação: 2006
Outros Autores: Chapchap,Paulo, Sredni,Simone Treiger, Viana,Cristiano Ribeiro, Mendes,Wellington Luiz
Tipo de documento: Artigo
Idioma: eng
Título da fonte: São Paulo medical journal (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802006000100005
Resumo: 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 serosa. 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 carcinoid 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 adjuvant treatment.
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spelling Childhood carcinoid tumors: description of a case series in a Brazilian cancer centerCarcinoid tumorNeuroendocrine tumorsDiagnosis. PathologySurgeryCONTEXT 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 serosa. 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 carcinoid 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 adjuvant treatment.Associação Paulista de Medicina - APM2006-02-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802006000100005Sao Paulo Medical Journal v.124 n.1 2006reponame:São Paulo medical journal (Online)instname:Associação Paulista de Medicinainstacron:APM10.1590/S1516-31802006000100005info:eu-repo/semantics/openAccessNeves,Gustavo RibeiroChapchap,PauloSredni,Simone TreigerViana,Cristiano RibeiroMendes,Wellington Luizeng2006-03-30T00:00:00Zoai:scielo:S1516-31802006000100005Revistahttp://www.scielo.br/spmjhttps://old.scielo.br/oai/scielo-oai.phprevistas@apm.org.br1806-94601516-3180opendoar:2006-03-30T00:00São 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
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
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 Carcinoid tumor
Neuroendocrine tumors
Diagnosis. Pathology
Surgery
topic 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 serosa. 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 carcinoid 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 adjuvant treatment.
publishDate 2006
dc.date.none.fl_str_mv 2006-02-01
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dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-31802006000100005
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dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv 10.1590/S1516-31802006000100005
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Associação Paulista de Medicina - APM
publisher.none.fl_str_mv Associação Paulista de Medicina - APM
dc.source.none.fl_str_mv Sao Paulo Medical Journal v.124 n.1 2006
reponame:São Paulo medical journal (Online)
instname:Associação Paulista de Medicina
instacron:APM
instname_str Associação Paulista de Medicina
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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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