Sarcoma granulocítico em órbita: relato de caso
Autor(a) principal: | |
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Data de Publicação: | 2005 |
Outros Autores: | , , , |
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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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) |
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UNIFESP |
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UNIFESP |
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Repositório Institucional da UNIFESP |
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Repositório Institucional da UNIFESP |
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Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
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1814268367698132992 |