Mixed-Cell Type Choroidal Melanoma in a Middle-Aged Woman

Detalhes bibliográficos
Autor(a) principal: Frinhani , Mirelly Aparecida Nolasco
Data de Publicação: 2023
Outros Autores: Pestana, Rebeca Alves, Dantas, Giuliane Stefane Braga, Bastianello , Matheus Alves, Ferreira, Filipe de Carvalho Emery, Altoé, Karina Coutinho, Franzin, Marcielle Grobério, Marcolongo-Pereira, Clairton, Chiarelli-Neto, Orlando
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista Brasileira de Cancerologia (Online)
Texto Completo: https://rbc.inca.gov.br/index.php/revista/article/view/3890
Resumo: Introduction: Melanomas are malignant neoplasms that occur in various anatomical sites, including the eye. Ocular melanomas account for 5% of all melanomas and are mainly described in Caucasian and older individuals. This study describes the clinical and pathological characteristics of uveal (choroid) melanoma in a Caucasian patient. Case report: A 41-year-old Caucasian female patient, brown eyes, without history of ophthalmological diseases or family history of cancer experienced pain and loss of visual acuity in the left eye. On clinical examination, an increase of ocular pressure was detected. Ultrasound showed a mushroom-like neoformation. Moreover, magnetic resonance imaging showed a mass with spontaneous hypersignal on T1-weighted images, intense gadolinium enhancement, and marked hyposignal on T2-weighted images. The patient was referred to the Oncology Ophthalmology department for enucleation due to suspected uveal melanoma. Anatomopathological analysis revealed a blackened mass in the eyeball. Histologically, the mass comprised spindle cells (50%) and epithelioid cells (50%). A diagnosis of choroidal melanoma was established based on the identification of ophthalmoscopic, imaging, and histological characteristics of the tumor. Conclusion: Choroidal melanomas usually occur in males, clear-eyed, and older individuals. A wide variety of ocular lesions may mimic choroidal melanoma, which should be included in the differential diagnosis of choroidal nevus and peripheral hemorrhages.
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spelling Mixed-Cell Type Choroidal Melanoma in a Middle-Aged WomanMelanoma Coroideo de Tipo Mixto en una Mujer de Mediana EdadMelanoma de Coroide do Tipo Misto em uma Mulher de Meia-Idadechoroid neoplasmsmelanomaeye enucleationeye painneoplasias da coroidemelanomaenucleação oculardor ocularneoplasias de la coroidesmelanomaenucleación del ojodolor ocularIntroduction: Melanomas are malignant neoplasms that occur in various anatomical sites, including the eye. Ocular melanomas account for 5% of all melanomas and are mainly described in Caucasian and older individuals. This study describes the clinical and pathological characteristics of uveal (choroid) melanoma in a Caucasian patient. Case report: A 41-year-old Caucasian female patient, brown eyes, without history of ophthalmological diseases or family history of cancer experienced pain and loss of visual acuity in the left eye. On clinical examination, an increase of ocular pressure was detected. Ultrasound showed a mushroom-like neoformation. Moreover, magnetic resonance imaging showed a mass with spontaneous hypersignal on T1-weighted images, intense gadolinium enhancement, and marked hyposignal on T2-weighted images. The patient was referred to the Oncology Ophthalmology department for enucleation due to suspected uveal melanoma. Anatomopathological analysis revealed a blackened mass in the eyeball. Histologically, the mass comprised spindle cells (50%) and epithelioid cells (50%). A diagnosis of choroidal melanoma was established based on the identification of ophthalmoscopic, imaging, and histological characteristics of the tumor. Conclusion: Choroidal melanomas usually occur in males, clear-eyed, and older individuals. A wide variety of ocular lesions may mimic choroidal melanoma, which should be included in the differential diagnosis of choroidal nevus and peripheral hemorrhages.Introducción: Los melanomas son neoplasias malignas que se presentan en varios sitios anatómicos, incluido el ojo. Los melanomas oculares representan el 5% de todos los melanomas y se describen principalmente en individuos caucásicos y de mayor edad. Este estudio describe las características clínicas y patológicas del melanoma uveal (coroides) en un paciente caucásico. Informe del caso: Paciente femenino de 41 años, caucásica, ojos marrones, sin antecedentes de enfermedades oftalmológicas y sin antecedentes familiares de cáncer, que consulta por dolor y pérdida de agudeza visual en el ojo izquierdo. En el examen clínico se observó aumento de la presión ocular. La ecografía mostró una neoformación con aspecto de hongo y la resonancia magnética mostró una masa con hiperseñal espontánea en T1, realce intenso de gadolinio y marcada hiposeñal en T2. La paciente fue remitida para cirugía de enucleación por sospecha de melanoma uveal. Se realizó análisis anatomopatológico, el cual mostró una masa ennegrecida en el interior del globo ocular. Histológicamente, la masa constaba de un 50 % de células fusiformes y un 50 % de células epitelioides. El diagnóstico de melanoma de coroides se basó en las características oftalmoscópicas, imagenológicas e histológicas del tumor. Conclusión: Los melanomas coroideos generalmente ocurren en pacientes masculinos, de ojos claros y de edad avanzada. Se advierte que una amplia variedad de lesiones oculares puede asemejarse al melanoma coroideo, y esto debe incluirse en el diagnóstico diferencial de nevus coroideo y hemorragias periféricas.Introdução: Melanomas são neoplasias malignas que ocorrem em vários sítios anatômicos, incluindo o olho. Os melanomas oculares correspondem a 5% de todos os melanomas e são descritos principalmente em indivíduos caucasianos e idosos. Este estudo descreve as características clinicopatológicas de um caso de melanoma uveal (coroide) em um paciente caucasiano. Relato do caso: Paciente, sexo feminino, 41 anos, caucasiana, olhos castanhos, sem antecedentes de doenças oftalmológicas e sem história familiar de câncer, com queixa de dor e perda da acuidade visual no olho esquerdo. No exame clínico, observou-se aumento da pressão ocular. O ultrassom revelou neoformação com aspecto de cogumelo, e a ressonância magnética, massa com hipersinal espontâneo em T1, intenso realce pelo gadolínio e marcado hipossinal em T2. A paciente foi encaminhada para cirurgia de enucleação em razão da suspeita de melanoma uveal. Foi realizada análise anatomopatológica que evidenciou massa enegrecida no interior do globo ocular. Histologicamente, a massa era constituída por 50% de células fusiformes e 50% de células epitelioides. O diagnóstico de melanoma de coroide baseou-se nas características oftalmoscópicas, imaginológicas e histológicas do tumor. Conclusão: Melanomas de coroide geralmente ocorrem em pacientes do sexo masculino, de olhos claros e idosos. Alerta-se que uma grande variedade de lesões oculares pode se assemelhar ao melanoma de coroide e este deve ser considerado no diagnóstico diferencial de nevo de coroide e hemorragias periféricas.INCA2023-05-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionRelato de Casoapplication/pdftext/htmlhttps://rbc.inca.gov.br/index.php/revista/article/view/389010.32635/2176-9745.RBC.2023v69n2.3890Revista Brasileira de Cancerologia; Vol. 69 No. 2 (2023): Apr./May/June; e-203890Revista Brasileira de Cancerologia; Vol. 69 Núm. 2 (2023): abr./mayo/jun.; e-203890Revista Brasileira de Cancerologia; v. 69 n. 2 (2023): abr./maio/jun.; e-2038902176-9745reponame:Revista Brasileira de Cancerologia (Online)instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)instacron:INCAenghttps://rbc.inca.gov.br/index.php/revista/article/view/3890/2851https://rbc.inca.gov.br/index.php/revista/article/view/3890/2854Copyright (c) 2023 Revista Brasileira de Cancerologiahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessFrinhani , Mirelly Aparecida NolascoPestana, Rebeca AlvesDantas, Giuliane Stefane BragaBastianello , Matheus AlvesFerreira, Filipe de Carvalho EmeryAltoé, Karina CoutinhoFranzin, Marcielle GrobérioMarcolongo-Pereira, ClairtonChiarelli-Neto, Orlando2023-06-16T20:31:44Zoai:rbc.inca.gov.br:article/3890Revistahttps://rbc.inca.gov.br/index.php/revistaPUBhttps://rbc.inca.gov.br/index.php/revista/oairbc@inca.gov.br0034-71162176-9745opendoar:2023-06-16T20:31:44Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)false
dc.title.none.fl_str_mv Mixed-Cell Type Choroidal Melanoma in a Middle-Aged Woman
Melanoma Coroideo de Tipo Mixto en una Mujer de Mediana Edad
Melanoma de Coroide do Tipo Misto em uma Mulher de Meia-Idade
title Mixed-Cell Type Choroidal Melanoma in a Middle-Aged Woman
spellingShingle Mixed-Cell Type Choroidal Melanoma in a Middle-Aged Woman
Frinhani , Mirelly Aparecida Nolasco
choroid neoplasms
melanoma
eye enucleation
eye pain
neoplasias da coroide
melanoma
enucleação ocular
dor ocular
neoplasias de la coroides
melanoma
enucleación del ojo
dolor ocular
title_short Mixed-Cell Type Choroidal Melanoma in a Middle-Aged Woman
title_full Mixed-Cell Type Choroidal Melanoma in a Middle-Aged Woman
title_fullStr Mixed-Cell Type Choroidal Melanoma in a Middle-Aged Woman
title_full_unstemmed Mixed-Cell Type Choroidal Melanoma in a Middle-Aged Woman
title_sort Mixed-Cell Type Choroidal Melanoma in a Middle-Aged Woman
author Frinhani , Mirelly Aparecida Nolasco
author_facet Frinhani , Mirelly Aparecida Nolasco
Pestana, Rebeca Alves
Dantas, Giuliane Stefane Braga
Bastianello , Matheus Alves
Ferreira, Filipe de Carvalho Emery
Altoé, Karina Coutinho
Franzin, Marcielle Grobério
Marcolongo-Pereira, Clairton
Chiarelli-Neto, Orlando
author_role author
author2 Pestana, Rebeca Alves
Dantas, Giuliane Stefane Braga
Bastianello , Matheus Alves
Ferreira, Filipe de Carvalho Emery
Altoé, Karina Coutinho
Franzin, Marcielle Grobério
Marcolongo-Pereira, Clairton
Chiarelli-Neto, Orlando
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Frinhani , Mirelly Aparecida Nolasco
Pestana, Rebeca Alves
Dantas, Giuliane Stefane Braga
Bastianello , Matheus Alves
Ferreira, Filipe de Carvalho Emery
Altoé, Karina Coutinho
Franzin, Marcielle Grobério
Marcolongo-Pereira, Clairton
Chiarelli-Neto, Orlando
dc.subject.por.fl_str_mv choroid neoplasms
melanoma
eye enucleation
eye pain
neoplasias da coroide
melanoma
enucleação ocular
dor ocular
neoplasias de la coroides
melanoma
enucleación del ojo
dolor ocular
topic choroid neoplasms
melanoma
eye enucleation
eye pain
neoplasias da coroide
melanoma
enucleação ocular
dor ocular
neoplasias de la coroides
melanoma
enucleación del ojo
dolor ocular
description Introduction: Melanomas are malignant neoplasms that occur in various anatomical sites, including the eye. Ocular melanomas account for 5% of all melanomas and are mainly described in Caucasian and older individuals. This study describes the clinical and pathological characteristics of uveal (choroid) melanoma in a Caucasian patient. Case report: A 41-year-old Caucasian female patient, brown eyes, without history of ophthalmological diseases or family history of cancer experienced pain and loss of visual acuity in the left eye. On clinical examination, an increase of ocular pressure was detected. Ultrasound showed a mushroom-like neoformation. Moreover, magnetic resonance imaging showed a mass with spontaneous hypersignal on T1-weighted images, intense gadolinium enhancement, and marked hyposignal on T2-weighted images. The patient was referred to the Oncology Ophthalmology department for enucleation due to suspected uveal melanoma. Anatomopathological analysis revealed a blackened mass in the eyeball. Histologically, the mass comprised spindle cells (50%) and epithelioid cells (50%). A diagnosis of choroidal melanoma was established based on the identification of ophthalmoscopic, imaging, and histological characteristics of the tumor. Conclusion: Choroidal melanomas usually occur in males, clear-eyed, and older individuals. A wide variety of ocular lesions may mimic choroidal melanoma, which should be included in the differential diagnosis of choroidal nevus and peripheral hemorrhages.
publishDate 2023
dc.date.none.fl_str_mv 2023-05-12
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Relato de Caso
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dc.identifier.uri.fl_str_mv https://rbc.inca.gov.br/index.php/revista/article/view/3890
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url https://rbc.inca.gov.br/index.php/revista/article/view/3890
identifier_str_mv 10.32635/2176-9745.RBC.2023v69n2.3890
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://rbc.inca.gov.br/index.php/revista/article/view/3890/2851
https://rbc.inca.gov.br/index.php/revista/article/view/3890/2854
dc.rights.driver.fl_str_mv Copyright (c) 2023 Revista Brasileira de Cancerologia
https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2023 Revista Brasileira de Cancerologia
https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
text/html
dc.publisher.none.fl_str_mv INCA
publisher.none.fl_str_mv INCA
dc.source.none.fl_str_mv Revista Brasileira de Cancerologia; Vol. 69 No. 2 (2023): Apr./May/June; e-203890
Revista Brasileira de Cancerologia; Vol. 69 Núm. 2 (2023): abr./mayo/jun.; e-203890
Revista Brasileira de Cancerologia; v. 69 n. 2 (2023): abr./maio/jun.; e-203890
2176-9745
reponame:Revista Brasileira de Cancerologia (Online)
instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
instacron:INCA
instname_str Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
instacron_str INCA
institution INCA
reponame_str Revista Brasileira de Cancerologia (Online)
collection Revista Brasileira de Cancerologia (Online)
repository.name.fl_str_mv Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
repository.mail.fl_str_mv rbc@inca.gov.br
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