Melanocitoma do nervo óptico

Detalhes bibliográficos
Autor(a) principal: Gouveia, Enéias Bezerra
Data de Publicação: 2008
Outros Autores: Morales, Maira Saad De Ávila [UNIFESP]
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1590/S0034-72802008000600010
http://repositorio.unifesp.br/handle/11600/4674
Resumo: Melanocytoma of the optic disc is a well known variant of melanocytic nevus that usually occurs as a deeply pigmented lesion on the head of the optic disc. Historically, this tumor has often been confused with malignant melanoma. Histopathologically, it is composed of deeply pigmented round oval cells with abundant cytoplasm and small, round, bland nuclei. Melanocytomas is a benign, stationary tumors, with almost no propensity to undergo malignant transformation. Most cases that occur on the optic disc are visually asymptomatic, but they can cause an afferent pupillary and visual field defects. Importantly, it can exhibit malignant transformation into melanoma in 1 to 2% of the cases. The affected patients should have periodic follow up.
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spelling Melanocitoma do nervo ópticoOptic disk melanocytoma: bibliographic reviewMelanomaOptic diskOptic nerve neoplasmsMelanocytesDiagnosis, differentialReviewMelanomaDisco ópticoNeoplasias do nervo ópticoMelanócitosDiagnóstico diferencialRevisãoMelanocytoma of the optic disc is a well known variant of melanocytic nevus that usually occurs as a deeply pigmented lesion on the head of the optic disc. Historically, this tumor has often been confused with malignant melanoma. Histopathologically, it is composed of deeply pigmented round oval cells with abundant cytoplasm and small, round, bland nuclei. Melanocytomas is a benign, stationary tumors, with almost no propensity to undergo malignant transformation. Most cases that occur on the optic disc are visually asymptomatic, but they can cause an afferent pupillary and visual field defects. Importantly, it can exhibit malignant transformation into melanoma in 1 to 2% of the cases. The affected patients should have periodic follow up.O melanocitoma do disco óptico é bem conhecido como uma variante do nervo melanocítico que geralmente ocorre no disco óptico. Historicamente o tumor foi confundido com melanoma maligno. Histopatologicamente é composto por células redondas densamente pigmentadas com citoplasma abundante e pequenos nucléolos. O melanocitoma é considerado um tumor benigno, estacionário e com pouca predisposição de sofrer malignação. Na maioria dos casos são assintomáticos, mas podem apresentar defeitos pupilares e no campo visual. É importante salientar que a transformação maligna em melanoma ocorre em 1 a 2% dos casos. Assim, os oftalmologistas devem familiarizar-se com o melanocitoma do disco óptico e os pacientes afetados devem ser acompanhados periodicamente.Centro Médico AvimedUniversidade Federal de São Paulo (UNIFESP) Escola Paulista de MedicinaUNIFESP, EPMSciELOSociedade Brasileira de OftalmologiaCentro Médico AvimedUniversidade Federal de São Paulo (UNIFESP)Gouveia, Enéias BezerraMorales, Maira Saad De Ávila [UNIFESP]2015-06-14T13:38:51Z2015-06-14T13:38:51Z2008-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion321-326application/pdfhttp://dx.doi.org/10.1590/S0034-72802008000600010Revista Brasileira de Oftalmologia. Sociedade Brasileira de Oftalmologia, v. 67, n. 6, p. 321-326, 2008.10.1590/S0034-72802008000600010S0034-72802008000600010.pdf0034-7280S0034-72802008000600010http://repositorio.unifesp.br/handle/11600/4674porRevista Brasileira de Oftalmologiainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-04T21:04:42Zoai:repositorio.unifesp.br/:11600/4674Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-04T21:04:42Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Melanocitoma do nervo óptico
Optic disk melanocytoma: bibliographic review
title Melanocitoma do nervo óptico
spellingShingle Melanocitoma do nervo óptico
Gouveia, Enéias Bezerra
Melanoma
Optic disk
Optic nerve neoplasms
Melanocytes
Diagnosis, differential
Review
Melanoma
Disco óptico
Neoplasias do nervo óptico
Melanócitos
Diagnóstico diferencial
Revisão
title_short Melanocitoma do nervo óptico
title_full Melanocitoma do nervo óptico
title_fullStr Melanocitoma do nervo óptico
title_full_unstemmed Melanocitoma do nervo óptico
title_sort Melanocitoma do nervo óptico
author Gouveia, Enéias Bezerra
author_facet Gouveia, Enéias Bezerra
Morales, Maira Saad De Ávila [UNIFESP]
author_role author
author2 Morales, Maira Saad De Ávila [UNIFESP]
author2_role author
dc.contributor.none.fl_str_mv Centro Médico Avimed
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Gouveia, Enéias Bezerra
Morales, Maira Saad De Ávila [UNIFESP]
dc.subject.por.fl_str_mv Melanoma
Optic disk
Optic nerve neoplasms
Melanocytes
Diagnosis, differential
Review
Melanoma
Disco óptico
Neoplasias do nervo óptico
Melanócitos
Diagnóstico diferencial
Revisão
topic Melanoma
Optic disk
Optic nerve neoplasms
Melanocytes
Diagnosis, differential
Review
Melanoma
Disco óptico
Neoplasias do nervo óptico
Melanócitos
Diagnóstico diferencial
Revisão
description Melanocytoma of the optic disc is a well known variant of melanocytic nevus that usually occurs as a deeply pigmented lesion on the head of the optic disc. Historically, this tumor has often been confused with malignant melanoma. Histopathologically, it is composed of deeply pigmented round oval cells with abundant cytoplasm and small, round, bland nuclei. Melanocytomas is a benign, stationary tumors, with almost no propensity to undergo malignant transformation. Most cases that occur on the optic disc are visually asymptomatic, but they can cause an afferent pupillary and visual field defects. Importantly, it can exhibit malignant transformation into melanoma in 1 to 2% of the cases. The affected patients should have periodic follow up.
publishDate 2008
dc.date.none.fl_str_mv 2008-12-01
2015-06-14T13:38:51Z
2015-06-14T13:38:51Z
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/S0034-72802008000600010
Revista Brasileira de Oftalmologia. Sociedade Brasileira de Oftalmologia, v. 67, n. 6, p. 321-326, 2008.
10.1590/S0034-72802008000600010
S0034-72802008000600010.pdf
0034-7280
S0034-72802008000600010
http://repositorio.unifesp.br/handle/11600/4674
url http://dx.doi.org/10.1590/S0034-72802008000600010
http://repositorio.unifesp.br/handle/11600/4674
identifier_str_mv Revista Brasileira de Oftalmologia. Sociedade Brasileira de Oftalmologia, v. 67, n. 6, p. 321-326, 2008.
10.1590/S0034-72802008000600010
S0034-72802008000600010.pdf
0034-7280
S0034-72802008000600010
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Revista Brasileira de Oftalmologia
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 321-326
application/pdf
dc.publisher.none.fl_str_mv Sociedade Brasileira de Oftalmologia
publisher.none.fl_str_mv Sociedade Brasileira 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
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