Childhood carcinoid tumors: description of a case series in a Brazilian cancer center
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Publication Date: | 2006 |
Other Authors: | , , , |
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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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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1825135073172652032 |