Achados histopatológicos em retinoblastoma

Detalhes bibliográficos
Autor(a) principal: Souza Filho, João Pessoa de [UNIFESP]
Data de Publicação: 2005
Outros Autores: Martins, Maria Cristina [UNIFESP], Torres, Virgínia Laura [UNIFESP], Dias, Ana Beatriz Toledo [UNIFESP], Lowen, Marcia Serva [UNIFESP], Pires, Luciana Afonso [UNIFESP], Erwenne, Clélia Maria [UNIFESP]
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1590/S0004-27492005000300010
http://repositorio.unifesp.br/handle/11600/2582
Resumo: OBJETIVO: To study histopathological findings of enucleated eyes with retinoblastoma. METHODS: Twenty-eight cases of retinoblastoma treated by enucleation at the Federal University of São Paulo from December 2000 to October 2002 were histopathologically reviewed. Clinical data included age, gender, race, unilateral or bilateral involvement and previous treatment. The histopathological review evaluated the presence of iris and/or angle neovascularization, tumor differentiation and optic nerve and choroidal invasion according to Khelfaoui's classification. RESULTS: Of 27 patients, 13 (48.5%) were boys and 14 (59.3%) were girls, 16 were white, 6 were black and 5 were asiatic, age ranging from 2 to 96 months (mean, 22.7 months). 13 cases were bilateral and 14 cases were unilateral. All tumors were histologically characterized by a proliferation of small cells with high nuclear-to-cytoplasmic ratios and 20 (71.4%) of them were well differentiated. Choroidal involvement was observed in 18 (64.2%) cases (degree II, III) and optic nerve invasion in 8 (28.5%) cases (degree III, IV, V). CONCLUSION: Neovascularization, necrosis and calcification were the most commonly observed feature. The invasion into the optic nerve and choroid, which are the two most important predictors of patient outcome were found in 28.5% and 64.2% of the cases, respectively.
id UFSP_2786bab0d70866d65ed4f649902cbe91
oai_identifier_str oai:repositorio.unifesp.br/:11600/2582
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling Achados histopatológicos em retinoblastomaHistopathologic findings in retinoblastomaRetinoblastomaChoroid neoplasmsOptic nerve neoplasmsNeoplasms invasivenessRisk factorsRetinoblastomaNeoplasias da coróideNeoplasias do nervo ópticoInvasividade neoplásicaFatores de riscoOBJETIVO: To study histopathological findings of enucleated eyes with retinoblastoma. METHODS: Twenty-eight cases of retinoblastoma treated by enucleation at the Federal University of São Paulo from December 2000 to October 2002 were histopathologically reviewed. Clinical data included age, gender, race, unilateral or bilateral involvement and previous treatment. The histopathological review evaluated the presence of iris and/or angle neovascularization, tumor differentiation and optic nerve and choroidal invasion according to Khelfaoui's classification. RESULTS: Of 27 patients, 13 (48.5%) were boys and 14 (59.3%) were girls, 16 were white, 6 were black and 5 were asiatic, age ranging from 2 to 96 months (mean, 22.7 months). 13 cases were bilateral and 14 cases were unilateral. All tumors were histologically characterized by a proliferation of small cells with high nuclear-to-cytoplasmic ratios and 20 (71.4%) of them were well differentiated. Choroidal involvement was observed in 18 (64.2%) cases (degree II, III) and optic nerve invasion in 8 (28.5%) cases (degree III, IV, V). CONCLUSION: Neovascularization, necrosis and calcification were the most commonly observed feature. The invasion into the optic nerve and choroid, which are the two most important predictors of patient outcome were found in 28.5% and 64.2% of the cases, respectively.OBJETIVO: Descrever e analisar os principais achados histopatológicos no retinoblastoma com ênfase na invasão de nervo óptico e túnicas oculares, correlacionando-os ao tratamento realizado. MÉTODOS: Vinte e oito olhos com diagnóstico de retinoblastoma tratados por enucleação na Universidade Federal de São Paulo (UNIFESP) entre dezembro de 2000 e outubro de 2002 foram submetidos à revisão histopatológica. Os dados clínicos incluiram idade, sexo, raça, lateralidade e tratamento realizado. Na revisão histopatológica foram avaliados neovascularização da íris e seio camerular, grau de diferenciação do tumor e invasão do nervo óptico e coróide de acordo com a classificação de Khelfaoui. RESULTADOS: De 27 pacientes, 13 (48,1%) eram do sexo masculino e 14 (51,9%) eram do sexo feminino, 16 (59,3%) eram da raça branca, 5 (18,5%) eram da raça amarela, 4 (14,8%) eram pardos e 2 (7,4%) eram negros. A média da idade dos pacientes foi de 22,7 meses, sendo 13 casos bilaterais e 14 casos unilaterais. Com relação ao tratamento utilizado, 13 (46,4%) olhos foram submetidos a enucleação primária e 15 (53,6%) tiveram tratamento prévio. Na avaliação histopatológica, 15 (53,6%) tumores eram bem diferenciados. Neovascularização da íris e/ou seio camerular foram observados em 60,6% e necrose e calcificação em 89,2% dos casos. O envolvimento da coróide foi observado em 18 (64,2%) dos casos (grau II e III) e a invasão de nervo óptico em 8 (28,5%) (graus II, III e IV). Dos casos submetidos ao tratamento prévio 40% tinham algum grau de invasão das túnicas oculares e apenas 6,67% apresentavam simultaneamente invasão do nervo óptico e das túnicas oculares. Entretanto nos olhos que foram submetidos à enucleação primária 30,7% apresentavam invasão das túnicas oculares e 53,8% apresentavam simultaneamente invasão do nervo óptico e das túnicas oculares. CONCLUSÃO: Neovascularização, necrose e calcificação foram achados mais comumente observados. A invasão do nervo óptico e coróide foram os dois fatores prognósticos mais importantes, encontrados em 28,5% e 64,2% dos casos respectivamente. Os casos tratados com enucleação primária apresentavam maior comprometimento ocular.Universidade Federal de São Paulo (UNIFESP) Departamento de OftalmologiaUNIFESP Departamento de Anatomia PatológicaUNIFESP, Depto. de OftalmologiaUNIFESP, Depto. de Anatomia PatológicaSciELOConselho Brasileiro de OftalmologiaUniversidade Federal de São Paulo (UNIFESP)Souza Filho, João Pessoa de [UNIFESP]Martins, Maria Cristina [UNIFESP]Torres, Virgínia Laura [UNIFESP]Dias, Ana Beatriz Toledo [UNIFESP]Lowen, Marcia Serva [UNIFESP]Pires, Luciana Afonso [UNIFESP]Erwenne, Clélia Maria [UNIFESP]2015-06-14T13:31:39Z2015-06-14T13:31:39Z2005-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion327-331application/pdfhttp://dx.doi.org/10.1590/S0004-27492005000300010Arquivos Brasileiros de Oftalmologia. Conselho Brasileiro de Oftalmologia, v. 68, n. 3, p. 327-331, 2005.10.1590/S0004-27492005000300010S0004-27492005000300010.pdf0004-2749S0004-27492005000300010http://repositorio.unifesp.br/handle/11600/2582porArquivos Brasileiros de Oftalmologiainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-29T10:38:19Zoai:repositorio.unifesp.br/:11600/2582Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-29T10:38:19Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Achados histopatológicos em retinoblastoma
Histopathologic findings in retinoblastoma
title Achados histopatológicos em retinoblastoma
spellingShingle Achados histopatológicos em retinoblastoma
Souza Filho, João Pessoa de [UNIFESP]
Retinoblastoma
Choroid neoplasms
Optic nerve neoplasms
Neoplasms invasiveness
Risk factors
Retinoblastoma
Neoplasias da coróide
Neoplasias do nervo óptico
Invasividade neoplásica
Fatores de risco
title_short Achados histopatológicos em retinoblastoma
title_full Achados histopatológicos em retinoblastoma
title_fullStr Achados histopatológicos em retinoblastoma
title_full_unstemmed Achados histopatológicos em retinoblastoma
title_sort Achados histopatológicos em retinoblastoma
author Souza Filho, João Pessoa de [UNIFESP]
author_facet Souza Filho, João Pessoa de [UNIFESP]
Martins, Maria Cristina [UNIFESP]
Torres, Virgínia Laura [UNIFESP]
Dias, Ana Beatriz Toledo [UNIFESP]
Lowen, Marcia Serva [UNIFESP]
Pires, Luciana Afonso [UNIFESP]
Erwenne, Clélia Maria [UNIFESP]
author_role author
author2 Martins, Maria Cristina [UNIFESP]
Torres, Virgínia Laura [UNIFESP]
Dias, Ana Beatriz Toledo [UNIFESP]
Lowen, Marcia Serva [UNIFESP]
Pires, Luciana Afonso [UNIFESP]
Erwenne, Clélia Maria [UNIFESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Souza Filho, João Pessoa de [UNIFESP]
Martins, Maria Cristina [UNIFESP]
Torres, Virgínia Laura [UNIFESP]
Dias, Ana Beatriz Toledo [UNIFESP]
Lowen, Marcia Serva [UNIFESP]
Pires, Luciana Afonso [UNIFESP]
Erwenne, Clélia Maria [UNIFESP]
dc.subject.por.fl_str_mv Retinoblastoma
Choroid neoplasms
Optic nerve neoplasms
Neoplasms invasiveness
Risk factors
Retinoblastoma
Neoplasias da coróide
Neoplasias do nervo óptico
Invasividade neoplásica
Fatores de risco
topic Retinoblastoma
Choroid neoplasms
Optic nerve neoplasms
Neoplasms invasiveness
Risk factors
Retinoblastoma
Neoplasias da coróide
Neoplasias do nervo óptico
Invasividade neoplásica
Fatores de risco
description OBJETIVO: To study histopathological findings of enucleated eyes with retinoblastoma. METHODS: Twenty-eight cases of retinoblastoma treated by enucleation at the Federal University of São Paulo from December 2000 to October 2002 were histopathologically reviewed. Clinical data included age, gender, race, unilateral or bilateral involvement and previous treatment. The histopathological review evaluated the presence of iris and/or angle neovascularization, tumor differentiation and optic nerve and choroidal invasion according to Khelfaoui's classification. RESULTS: Of 27 patients, 13 (48.5%) were boys and 14 (59.3%) were girls, 16 were white, 6 were black and 5 were asiatic, age ranging from 2 to 96 months (mean, 22.7 months). 13 cases were bilateral and 14 cases were unilateral. All tumors were histologically characterized by a proliferation of small cells with high nuclear-to-cytoplasmic ratios and 20 (71.4%) of them were well differentiated. Choroidal involvement was observed in 18 (64.2%) cases (degree II, III) and optic nerve invasion in 8 (28.5%) cases (degree III, IV, V). CONCLUSION: Neovascularization, necrosis and calcification were the most commonly observed feature. The invasion into the optic nerve and choroid, which are the two most important predictors of patient outcome were found in 28.5% and 64.2% of the cases, respectively.
publishDate 2005
dc.date.none.fl_str_mv 2005-06-01
2015-06-14T13:31:39Z
2015-06-14T13:31:39Z
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/S0004-27492005000300010
Arquivos Brasileiros de Oftalmologia. Conselho Brasileiro de Oftalmologia, v. 68, n. 3, p. 327-331, 2005.
10.1590/S0004-27492005000300010
S0004-27492005000300010.pdf
0004-2749
S0004-27492005000300010
http://repositorio.unifesp.br/handle/11600/2582
url http://dx.doi.org/10.1590/S0004-27492005000300010
http://repositorio.unifesp.br/handle/11600/2582
identifier_str_mv Arquivos Brasileiros de Oftalmologia. Conselho Brasileiro de Oftalmologia, v. 68, n. 3, p. 327-331, 2005.
10.1590/S0004-27492005000300010
S0004-27492005000300010.pdf
0004-2749
S0004-27492005000300010
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Arquivos Brasileiros de Oftalmologia
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 327-331
application/pdf
dc.publisher.none.fl_str_mv Conselho Brasileiro de Oftalmologia
publisher.none.fl_str_mv Conselho Brasileiro de Oftalmologia
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
_version_ 1814268325221367808