Sarcoma granulocítico em órbita: relato de caso

Detalhes bibliográficos
Autor(a) principal: Fonseca Junior, Nilson Lopes Da [UNIFESP]
Data de Publicação: 2005
Outros Autores: Paves, Luis [UNIFESP], Nakanami, Deise Mitsuko [UNIFESP], Seixas, Maria Teresa [UNIFESP], Manso, Paulo Góis [UNIFESP]
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1590/S0004-27492005000400026
http://repositorio.unifesp.br/handle/11600/2616
Resumo: Orbital granulocytic sarcoma is a localized tumor consisting of malignant cells of myeloid origin. This tumor may present in association with acute myelogenous leukemia. Granulocytic sarcoma may be found in a variety of locations throughout the body including the orbit and typically affects children and young adults. There is a slight male predominance in these cases. This is an uncommon case report of a 33-year-old Latin-American woman who was admitted to the Hospital for rapidly progressive orbital proptosis. There was no systemic manifestation of leukemia. The occurrence of orbital granulocytic sarcoma before the development of systemic leukemia in children and young adults is not uncommon and these cases frequently develop hematological evidence within 2 months after initial orbital disease. In this case report, there was no systemic manifestation of leukemia in the last 30 months, even in the presence of orbital tumors. Granulocytic sarcoma is most frequently confused with malignant lymphoma, rhabdomyosarcoma and neuroblastoma. The differential diagnosis of these cases can be challenging, particularly when there is no evidence of systemic leukemia, when imaging features are not sufficiently specific to distinguish granulocytic neoplasms from other tumors. To establish the diagnosis often a biopsy is required. The treatment in such cases (orbital granulocytic sarcoma) is not standardized. Orbital granulocytic sarcoma may be suspected in cases of orbital tumors even in the absence of systemic manifestations of leukemia at any age.
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spelling Sarcoma granulocítico em órbita: relato de casoOrbital granulocytic sarcoma: case reportLeukemia, myeloidOrbital neoplasmsSarcoma, granulocyticDiagnosis, differentialTomography, x-ray computedLeucemia mielóideNeoplasias OrbitáriasSarcoma, granulocíticoDiagnóstico diferencialTomografia computadorizada por raios XOrbital granulocytic sarcoma is a localized tumor consisting of malignant cells of myeloid origin. This tumor may present in association with acute myelogenous leukemia. Granulocytic sarcoma may be found in a variety of locations throughout the body including the orbit and typically affects children and young adults. There is a slight male predominance in these cases. This is an uncommon case report of a 33-year-old Latin-American woman who was admitted to the Hospital for rapidly progressive orbital proptosis. There was no systemic manifestation of leukemia. The occurrence of orbital granulocytic sarcoma before the development of systemic leukemia in children and young adults is not uncommon and these cases frequently develop hematological evidence within 2 months after initial orbital disease. In this case report, there was no systemic manifestation of leukemia in the last 30 months, even in the presence of orbital tumors. Granulocytic sarcoma is most frequently confused with malignant lymphoma, rhabdomyosarcoma and neuroblastoma. The differential diagnosis of these cases can be challenging, particularly when there is no evidence of systemic leukemia, when imaging features are not sufficiently specific to distinguish granulocytic neoplasms from other tumors. To establish the diagnosis often a biopsy is required. The treatment in such cases (orbital granulocytic sarcoma) is not standardized. Orbital granulocytic sarcoma may be suspected in cases of orbital tumors even in the absence of systemic manifestations of leukemia at any age.O sarcoma granulocítico é tumor que freqüentemente aparece em pacientes portadores de leucemia mielóide aguda, podendo aparecer em diferentes regiões do corpo, incluindo a órbita. Nesta última localização, é mais freqüente em crianças e adultos jovens, com discreta predominância em pacientes do sexo masculino. Este é um caso de sarcoma granulocítico orbitário de evolução rápida, sem manifestação sistêmica associada em uma paciente de 33 anos de idade, o que o torna incomum. O surgimento do sarcoma granulocítico orbitário sem acometimento leucêmico pode ocorrer em cerca de 88% dos pacientes com acometimento orbitário. A maioria dos pacientes apresenta evidências hematológicas de comprometimento sistêmico em 2 meses após a manifestação orbitária. Neste relato de caso, a paciente não apresenta acometimento sistêmico, apesar da manifestação orbitária estar presente há 30 meses. Os principais diagnósticos diferenciais do sarcoma granulocítico orbitário são o linfoma, o rabdomiossarcoma e o neuroblastoma. O diagnóstico pode ser dificultado, principalmente nos casos sem acometimento sistêmico, nos quais os exames de imagem e as manifestações clínicas pouco diferem de outras doenças. Para o diagnóstico deve-se realizar uma biópsia da lesão orbitária para análise anatomopatológica e imuno-histoquímica. O tratamento nos casos de sarcoma granulocítico orbitário sem acometimento sistêmico não é padronizado. A hipótese diagnóstica de sarcoma granulocítico orbitário deve ser aventada em casos de pacientes com tumoração orbitária mesmo que não apresentem sinais ou sintomas sistêmicos e independentes da faixa etária.Universidade Federal de São Paulo (UNIFESP) Departamento de Oftalmologia Setor de ÓrbitaUNIFESPUNIFESP, Depto. de Oftalmologia Setor de ÓrbitaUNIFESPSciELOConselho Brasileiro de OftalmologiaUniversidade Federal de São Paulo (UNIFESP)Fonseca Junior, Nilson Lopes Da [UNIFESP]Paves, Luis [UNIFESP]Nakanami, Deise Mitsuko [UNIFESP]Seixas, Maria Teresa [UNIFESP]Manso, Paulo Góis [UNIFESP]2015-06-14T13:31:41Z2015-06-14T13:31:41Z2005-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion557-560application/pdfhttp://dx.doi.org/10.1590/S0004-27492005000400026Arquivos Brasileiros de Oftalmologia. Conselho Brasileiro de Oftalmologia, v. 68, n. 4, p. 557-560, 2005.10.1590/S0004-27492005000400026S0004-27492005000400026.pdf0004-2749S0004-27492005000400026http://repositorio.unifesp.br/handle/11600/2616porArquivos Brasileiros de Oftalmologiainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-04T14:02:01Zoai:repositorio.unifesp.br/:11600/2616Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-04T14:02:01Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Sarcoma granulocítico em órbita: relato de caso
Orbital granulocytic sarcoma: case report
title Sarcoma granulocítico em órbita: relato de caso
spellingShingle Sarcoma granulocítico em órbita: relato de caso
Fonseca Junior, Nilson Lopes Da [UNIFESP]
Leukemia, myeloid
Orbital neoplasms
Sarcoma, granulocytic
Diagnosis, differential
Tomography, x-ray computed
Leucemia mielóide
Neoplasias Orbitárias
Sarcoma, granulocítico
Diagnóstico diferencial
Tomografia computadorizada por raios X
title_short Sarcoma granulocítico em órbita: relato de caso
title_full Sarcoma granulocítico em órbita: relato de caso
title_fullStr Sarcoma granulocítico em órbita: relato de caso
title_full_unstemmed Sarcoma granulocítico em órbita: relato de caso
title_sort Sarcoma granulocítico em órbita: relato de caso
author Fonseca Junior, Nilson Lopes Da [UNIFESP]
author_facet Fonseca Junior, Nilson Lopes Da [UNIFESP]
Paves, Luis [UNIFESP]
Nakanami, Deise Mitsuko [UNIFESP]
Seixas, Maria Teresa [UNIFESP]
Manso, Paulo Góis [UNIFESP]
author_role author
author2 Paves, Luis [UNIFESP]
Nakanami, Deise Mitsuko [UNIFESP]
Seixas, Maria Teresa [UNIFESP]
Manso, Paulo Góis [UNIFESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Fonseca Junior, Nilson Lopes Da [UNIFESP]
Paves, Luis [UNIFESP]
Nakanami, Deise Mitsuko [UNIFESP]
Seixas, Maria Teresa [UNIFESP]
Manso, Paulo Góis [UNIFESP]
dc.subject.por.fl_str_mv Leukemia, myeloid
Orbital neoplasms
Sarcoma, granulocytic
Diagnosis, differential
Tomography, x-ray computed
Leucemia mielóide
Neoplasias Orbitárias
Sarcoma, granulocítico
Diagnóstico diferencial
Tomografia computadorizada por raios X
topic Leukemia, myeloid
Orbital neoplasms
Sarcoma, granulocytic
Diagnosis, differential
Tomography, x-ray computed
Leucemia mielóide
Neoplasias Orbitárias
Sarcoma, granulocítico
Diagnóstico diferencial
Tomografia computadorizada por raios X
description Orbital granulocytic sarcoma is a localized tumor consisting of malignant cells of myeloid origin. This tumor may present in association with acute myelogenous leukemia. Granulocytic sarcoma may be found in a variety of locations throughout the body including the orbit and typically affects children and young adults. There is a slight male predominance in these cases. This is an uncommon case report of a 33-year-old Latin-American woman who was admitted to the Hospital for rapidly progressive orbital proptosis. There was no systemic manifestation of leukemia. The occurrence of orbital granulocytic sarcoma before the development of systemic leukemia in children and young adults is not uncommon and these cases frequently develop hematological evidence within 2 months after initial orbital disease. In this case report, there was no systemic manifestation of leukemia in the last 30 months, even in the presence of orbital tumors. Granulocytic sarcoma is most frequently confused with malignant lymphoma, rhabdomyosarcoma and neuroblastoma. The differential diagnosis of these cases can be challenging, particularly when there is no evidence of systemic leukemia, when imaging features are not sufficiently specific to distinguish granulocytic neoplasms from other tumors. To establish the diagnosis often a biopsy is required. The treatment in such cases (orbital granulocytic sarcoma) is not standardized. Orbital granulocytic sarcoma may be suspected in cases of orbital tumors even in the absence of systemic manifestations of leukemia at any age.
publishDate 2005
dc.date.none.fl_str_mv 2005-08-01
2015-06-14T13:31:41Z
2015-06-14T13:31:41Z
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/S0004-27492005000400026
Arquivos Brasileiros de Oftalmologia. Conselho Brasileiro de Oftalmologia, v. 68, n. 4, p. 557-560, 2005.
10.1590/S0004-27492005000400026
S0004-27492005000400026.pdf
0004-2749
S0004-27492005000400026
http://repositorio.unifesp.br/handle/11600/2616
url http://dx.doi.org/10.1590/S0004-27492005000400026
http://repositorio.unifesp.br/handle/11600/2616
identifier_str_mv Arquivos Brasileiros de Oftalmologia. Conselho Brasileiro de Oftalmologia, v. 68, n. 4, p. 557-560, 2005.
10.1590/S0004-27492005000400026
S0004-27492005000400026.pdf
0004-2749
S0004-27492005000400026
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 557-560
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
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