Rabdomiosarcoma de cabeça e pescoço na infância

Detalhes bibliográficos
Autor(a) principal: Neves, Beatrice Mª J. [UNIFESP]
Data de Publicação: 2003
Outros Autores: Pontes, Paulo A. de L. [UNIFESP], Caran, Eliana Maria Monteiro [UNIFESP], Figueiredo, Claudia [UNIFESP], Weckx, Luc Louis Maurice [UNIFESP], Fujita, Reginaldo Raimundo [UNIFESP]
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1590/S0034-72992003000100005
http://repositorio.unifesp.br/handle/11600/1623
Resumo: Rhabdomyosarcoma (RMS) is a malignant tumor of immature mesenchymal cells; it can arise from any part of the body. RMS is the most common soft tissue sarcomain the childhood and its most frequent primary site is the head and neck. AIM: The purpose of this study was to review the occurrence of head and neck RMS in childhood and its clinical-histopathologic features. STUDY DESIGN: Clinical retrospective. METHOD: Eighty-two patients with soft tissue sarcoma treated in the Institute of Pediatric Oncology, UNIFESP-EPM, between 1988 and 2002 were included in this study. The medical records of the patients with head and neck soft tissue sarcomas were reviewed. The following parameters were analyzed: incidence of RMS in the childhood and in the head and neck, sex, age, histological classification, primary site, follow-up. RESULTS: In this study, 65% of soft tissue sarcomas were RMS; 33% of RMS were in the head and neck region; 77% of soft tissue sarcoma in this region were RMS. The mean age at diagnosis was 7.62 years, 41% were between 5 and 9 years. In this sample, there were 47% men and 53% women. Embryonic RMS was the predominant histological type (64.6%) and the orbit was the most common primary site (52.8%). One hundred percent, 50% and 33.3% of the parameningeal, nonparameningeal and orbital RMS, respectively, led to death. CONCLUSION: RMS is the most common soft tissue sarcoma in the childhood and the head and neck is the most frequent primary site. Males were more affected by RMS than females. The mean age at diagnosis was 7.62 years and the most frequent age interval was between 5 and 9 years old. The embryonic histological type and the orbit as primary site were predominant. The highest mortality was found for parameningeal RMS and the lowest, for orbital RMS.
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spelling Rabdomiosarcoma de cabeça e pescoço na infânciaHead and neck rhabdomyosarcoma in childhoodrhabdomyosarcomapediatric oncologyhead and neck neoplasmrabdomiosarcomaoncologia pediátricaneoplasias de cabeça e pescoçoRhabdomyosarcoma (RMS) is a malignant tumor of immature mesenchymal cells; it can arise from any part of the body. RMS is the most common soft tissue sarcomain the childhood and its most frequent primary site is the head and neck. AIM: The purpose of this study was to review the occurrence of head and neck RMS in childhood and its clinical-histopathologic features. STUDY DESIGN: Clinical retrospective. METHOD: Eighty-two patients with soft tissue sarcoma treated in the Institute of Pediatric Oncology, UNIFESP-EPM, between 1988 and 2002 were included in this study. The medical records of the patients with head and neck soft tissue sarcomas were reviewed. The following parameters were analyzed: incidence of RMS in the childhood and in the head and neck, sex, age, histological classification, primary site, follow-up. RESULTS: In this study, 65% of soft tissue sarcomas were RMS; 33% of RMS were in the head and neck region; 77% of soft tissue sarcoma in this region were RMS. The mean age at diagnosis was 7.62 years, 41% were between 5 and 9 years. In this sample, there were 47% men and 53% women. Embryonic RMS was the predominant histological type (64.6%) and the orbit was the most common primary site (52.8%). One hundred percent, 50% and 33.3% of the parameningeal, nonparameningeal and orbital RMS, respectively, led to death. CONCLUSION: RMS is the most common soft tissue sarcoma in the childhood and the head and neck is the most frequent primary site. Males were more affected by RMS than females. The mean age at diagnosis was 7.62 years and the most frequent age interval was between 5 and 9 years old. The embryonic histological type and the orbit as primary site were predominant. The highest mortality was found for parameningeal RMS and the lowest, for orbital RMS.Rabdomiosarcoma é uma neoplasia maligna originária de células mesenquimais primitivas, podendo ocorrer em qualquer lugar do corpo. É o sarcoma de partes moles mais comum na infância, e localiza-se mais freqüentemente na cabeça e pescoço. OBJETIVO: Estudar a ocorrência de RMS na cabeça e pescoço na infância, correlacionando aspectos clínicos e histopatológicos. FORMA DE ESTUDO: Clínico retrospectivo. MÉTODO: Oitenta e dois pacientes com diagnóstico de sarcomas de partes moles, atendidos no Instituto de Oncopediatria da UNIFESP-EPM de 1988 a 2002 foram incluídos neste estudo. Foram estudados os seguintes parâmetros: incidência de RMS na infância e na cabeça e pescoço, distribuição segundo sexo, faixa etária, tipo histológico, localização primária, óbito X localização, causa mortis. RESULTADOS: Neste estudo 65% dos casos de sarcomas de partes moles corresponderam à RMS; 33% dos casos de RMS localizavam-se na cabeça e pescoço; 77% dos casos de sarcoma de partes moles de cabeça e pescoço corresponderam ao RMS. A média de idade no diagnóstico foi de 7,62 anos, predominando na faixa etária dos 5 aos 9 anos (41%). Em relação ao sexo, encontramos 47% do sexo feminino e 53% do sexo masculino. Quanto ao tipo histológico, o mais comum foi o RMS embrionário correspondendo a 64,6% do total. O sítio primário mais comum foi o orbital (52,8%). Cem por cento, 50% e 33,3% dos pacientes com RMS parameníngeo, não parameníngeo e orbital, respectivamente, evoluíram para óbito. CONCLUSÃO: O RMS é o sarcoma de partes moles mais comum na infância, localizando-se preferencialmente na cabeça e pescoço. Houve predominância do sexo masculino neste estudo; idade média de 7,62 anos predominando a faixa etária dos 5 aos 9 anos. O tipo histológico predominante foi o embrionário e a localização orbital foi mais freqüente. O maior índice de óbito pertenceu aos RMS parameníngeo e o menor ao orbital.Universidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Departamento de Otorrinolaringologia e Distúrbios da Comunicação HumanaUniversidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Instituto de OncopediatriaUniversidade Federal de São Paulo (UNIFESP) Escola Paulista de Medicina Disciplina de Otorrinolaringologia Pediátrica do Depto. de ORL-DCHUNIFESP, EPM, Depto. de Otorrinolaringologia e Distúrbios da Comunicação HumanaUNIFESP, EPM, Instituto de OncopediatriaUNIFESP, EPM, Disciplina de Otorrinolaringologia Pediátrica do Depto. de ORL-DCHSciELOABORL-CCF Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-FacialUniversidade Federal de São Paulo (UNIFESP)Neves, Beatrice Mª J. [UNIFESP]Pontes, Paulo A. de L. [UNIFESP]Caran, Eliana Maria Monteiro [UNIFESP]Figueiredo, Claudia [UNIFESP]Weckx, Luc Louis Maurice [UNIFESP]Fujita, Reginaldo Raimundo [UNIFESP]2015-06-14T13:29:54Z2015-06-14T13:29:54Z2003-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion24-28application/pdfhttp://dx.doi.org/10.1590/S0034-72992003000100005Revista Brasileira de Otorrinolaringologia. ABORL-CCF Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial, v. 69, n. 1, p. 24-28, 2003.10.1590/S0034-72992003000100005S0034-72992003000100005.pdf0034-7299S0034-72992003000100005http://repositorio.unifesp.br/handle/11600/1623porRevista Brasileira de Otorrinolaringologiainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-29T13:32:58Zoai:repositorio.unifesp.br/:11600/1623Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-29T13:32:58Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Rabdomiosarcoma de cabeça e pescoço na infância
Head and neck rhabdomyosarcoma in childhood
title Rabdomiosarcoma de cabeça e pescoço na infância
spellingShingle Rabdomiosarcoma de cabeça e pescoço na infância
Neves, Beatrice Mª J. [UNIFESP]
rhabdomyosarcoma
pediatric oncology
head and neck neoplasm
rabdomiosarcoma
oncologia pediátrica
neoplasias de cabeça e pescoço
title_short Rabdomiosarcoma de cabeça e pescoço na infância
title_full Rabdomiosarcoma de cabeça e pescoço na infância
title_fullStr Rabdomiosarcoma de cabeça e pescoço na infância
title_full_unstemmed Rabdomiosarcoma de cabeça e pescoço na infância
title_sort Rabdomiosarcoma de cabeça e pescoço na infância
author Neves, Beatrice Mª J. [UNIFESP]
author_facet Neves, Beatrice Mª J. [UNIFESP]
Pontes, Paulo A. de L. [UNIFESP]
Caran, Eliana Maria Monteiro [UNIFESP]
Figueiredo, Claudia [UNIFESP]
Weckx, Luc Louis Maurice [UNIFESP]
Fujita, Reginaldo Raimundo [UNIFESP]
author_role author
author2 Pontes, Paulo A. de L. [UNIFESP]
Caran, Eliana Maria Monteiro [UNIFESP]
Figueiredo, Claudia [UNIFESP]
Weckx, Luc Louis Maurice [UNIFESP]
Fujita, Reginaldo Raimundo [UNIFESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Neves, Beatrice Mª J. [UNIFESP]
Pontes, Paulo A. de L. [UNIFESP]
Caran, Eliana Maria Monteiro [UNIFESP]
Figueiredo, Claudia [UNIFESP]
Weckx, Luc Louis Maurice [UNIFESP]
Fujita, Reginaldo Raimundo [UNIFESP]
dc.subject.por.fl_str_mv rhabdomyosarcoma
pediatric oncology
head and neck neoplasm
rabdomiosarcoma
oncologia pediátrica
neoplasias de cabeça e pescoço
topic rhabdomyosarcoma
pediatric oncology
head and neck neoplasm
rabdomiosarcoma
oncologia pediátrica
neoplasias de cabeça e pescoço
description Rhabdomyosarcoma (RMS) is a malignant tumor of immature mesenchymal cells; it can arise from any part of the body. RMS is the most common soft tissue sarcomain the childhood and its most frequent primary site is the head and neck. AIM: The purpose of this study was to review the occurrence of head and neck RMS in childhood and its clinical-histopathologic features. STUDY DESIGN: Clinical retrospective. METHOD: Eighty-two patients with soft tissue sarcoma treated in the Institute of Pediatric Oncology, UNIFESP-EPM, between 1988 and 2002 were included in this study. The medical records of the patients with head and neck soft tissue sarcomas were reviewed. The following parameters were analyzed: incidence of RMS in the childhood and in the head and neck, sex, age, histological classification, primary site, follow-up. RESULTS: In this study, 65% of soft tissue sarcomas were RMS; 33% of RMS were in the head and neck region; 77% of soft tissue sarcoma in this region were RMS. The mean age at diagnosis was 7.62 years, 41% were between 5 and 9 years. In this sample, there were 47% men and 53% women. Embryonic RMS was the predominant histological type (64.6%) and the orbit was the most common primary site (52.8%). One hundred percent, 50% and 33.3% of the parameningeal, nonparameningeal and orbital RMS, respectively, led to death. CONCLUSION: RMS is the most common soft tissue sarcoma in the childhood and the head and neck is the most frequent primary site. Males were more affected by RMS than females. The mean age at diagnosis was 7.62 years and the most frequent age interval was between 5 and 9 years old. The embryonic histological type and the orbit as primary site were predominant. The highest mortality was found for parameningeal RMS and the lowest, for orbital RMS.
publishDate 2003
dc.date.none.fl_str_mv 2003-01-01
2015-06-14T13:29:54Z
2015-06-14T13:29:54Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0034-72992003000100005
Revista Brasileira de Otorrinolaringologia. ABORL-CCF Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial, v. 69, n. 1, p. 24-28, 2003.
10.1590/S0034-72992003000100005
S0034-72992003000100005.pdf
0034-7299
S0034-72992003000100005
http://repositorio.unifesp.br/handle/11600/1623
url http://dx.doi.org/10.1590/S0034-72992003000100005
http://repositorio.unifesp.br/handle/11600/1623
identifier_str_mv Revista Brasileira de Otorrinolaringologia. ABORL-CCF Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial, v. 69, n. 1, p. 24-28, 2003.
10.1590/S0034-72992003000100005
S0034-72992003000100005.pdf
0034-7299
S0034-72992003000100005
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Revista Brasileira de Otorrinolaringologia
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 24-28
application/pdf
dc.publisher.none.fl_str_mv ABORL-CCF Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial
publisher.none.fl_str_mv ABORL-CCF Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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