Malignant bone tumors in Pediatrics. Five year experience in a pediatric referral center
Background: Osteosarcoma (OS) and Ewing’s Sarcoma (ES) are the two most common malignant bone tumors in children. A retrospective review of the records of children diagnosed in a pediatric hospital over a five year period (2008-2013) was performed.Objective: To present the experiences acquired durin...
- Autores:
-
Barros, Gisela
Trujillo, Angela María
Jaramillo, Lina
Ortiz, Francy Helena
Contreras, Agustin Dario
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2016
- Institución:
- Universidad Nacional de Colombia
- Repositorio:
- Universidad Nacional de Colombia
- Idioma:
- spa
- OAI Identifier:
- oai:repositorio.unal.edu.co:unal/65187
- Acceso en línea:
- https://repositorio.unal.edu.co/handle/unal/65187
http://bdigital.unal.edu.co/66210/
- Palabra clave:
- 61 Ciencias médicas; Medicina / Medicine and health
Osteosarcoma
Ewing’s Sarcoma
Disease Progression
Recurrence
Neoplasm Metastasis
Osteosarcoma
Sarcoma de Ewing
Progresión de la enfermedad
Recurrencia
Metástasis de la neoplasia
- Rights
- openAccess
- License
- Atribución-NoComercial 4.0 Internacional
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UNACIONAL2 |
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Universidad Nacional de Colombia |
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|
dc.title.spa.fl_str_mv |
Malignant bone tumors in Pediatrics. Five year experience in a pediatric referral center |
title |
Malignant bone tumors in Pediatrics. Five year experience in a pediatric referral center |
spellingShingle |
Malignant bone tumors in Pediatrics. Five year experience in a pediatric referral center 61 Ciencias médicas; Medicina / Medicine and health Osteosarcoma Ewing’s Sarcoma Disease Progression Recurrence Neoplasm Metastasis Osteosarcoma Sarcoma de Ewing Progresión de la enfermedad Recurrencia Metástasis de la neoplasia |
title_short |
Malignant bone tumors in Pediatrics. Five year experience in a pediatric referral center |
title_full |
Malignant bone tumors in Pediatrics. Five year experience in a pediatric referral center |
title_fullStr |
Malignant bone tumors in Pediatrics. Five year experience in a pediatric referral center |
title_full_unstemmed |
Malignant bone tumors in Pediatrics. Five year experience in a pediatric referral center |
title_sort |
Malignant bone tumors in Pediatrics. Five year experience in a pediatric referral center |
dc.creator.fl_str_mv |
Barros, Gisela Trujillo, Angela María Jaramillo, Lina Ortiz, Francy Helena Contreras, Agustin Dario |
dc.contributor.author.spa.fl_str_mv |
Barros, Gisela Trujillo, Angela María Jaramillo, Lina Ortiz, Francy Helena Contreras, Agustin Dario |
dc.subject.ddc.spa.fl_str_mv |
61 Ciencias médicas; Medicina / Medicine and health |
topic |
61 Ciencias médicas; Medicina / Medicine and health Osteosarcoma Ewing’s Sarcoma Disease Progression Recurrence Neoplasm Metastasis Osteosarcoma Sarcoma de Ewing Progresión de la enfermedad Recurrencia Metástasis de la neoplasia |
dc.subject.proposal.spa.fl_str_mv |
Osteosarcoma Ewing’s Sarcoma Disease Progression Recurrence Neoplasm Metastasis Osteosarcoma Sarcoma de Ewing Progresión de la enfermedad Recurrencia Metástasis de la neoplasia |
description |
Background: Osteosarcoma (OS) and Ewing’s Sarcoma (ES) are the two most common malignant bone tumors in children. A retrospective review of the records of children diagnosed in a pediatric hospital over a five year period (2008-2013) was performed.Objective: To present the experiences acquired during the treatment of these types of tumors and to compare the results obtained with those reported in the literature.Methodology: The database of the Oncology and Pathology Service of Fundación Hospital de la Misericordia (HOMI) was reviewed to identify patients with primary bone tumors referred for histopathology analysis.Results: 22 patients were diagnosed with OS, with a mean age of 11.9 years. 96% of cases were located in the lower extremities. All patients received neoadjuvant chemotherapy and 86% underwent surgical treatment; 13% survived. 15 patients were diagnosed with ES, with a mean age of 12.4 years. 67% of cases were located in flat bones, 53% of patients had metastasis when diagnosed, and all received neoadjuvant chemotherapy. 40% of patients received surgical intervention and 20% received radiotherapy. Survival at the completion of the reseearch was 33%.Conclusions: Cure and survival rates are lower than those reported in the literature despite efforts to improve treatments. |
publishDate |
2016 |
dc.date.issued.spa.fl_str_mv |
2016-07-01 |
dc.date.accessioned.spa.fl_str_mv |
2019-07-02T23:57:30Z |
dc.date.available.spa.fl_str_mv |
2019-07-02T23:57:30Z |
dc.type.spa.fl_str_mv |
Artículo de revista |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.driver.spa.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.version.spa.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.coar.spa.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.coarversion.spa.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.content.spa.fl_str_mv |
Text |
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http://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/resource_type/c_6501 |
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publishedVersion |
dc.identifier.issn.spa.fl_str_mv |
ISSN: 2357-3848 |
dc.identifier.uri.none.fl_str_mv |
https://repositorio.unal.edu.co/handle/unal/65187 |
dc.identifier.eprints.spa.fl_str_mv |
http://bdigital.unal.edu.co/66210/ |
identifier_str_mv |
ISSN: 2357-3848 |
url |
https://repositorio.unal.edu.co/handle/unal/65187 http://bdigital.unal.edu.co/66210/ |
dc.language.iso.spa.fl_str_mv |
spa |
language |
spa |
dc.relation.spa.fl_str_mv |
https://revistas.unal.edu.co/index.php/revfacmed/article/view/50475 |
dc.relation.ispartof.spa.fl_str_mv |
Universidad Nacional de Colombia Revistas electrónicas UN Revista de la Facultad de Medicina Revista de la Facultad de Medicina |
dc.relation.references.spa.fl_str_mv |
Barros, Gisela and Trujillo, Angela María and Jaramillo, Lina and Ortiz, Francy Helena and Contreras, Agustin Dario (2016) Malignant bone tumors in Pediatrics. Five year experience in a pediatric referral center. Revista de la Facultad de Medicina, 64 (3). pp. 403-407. ISSN 2357-3848 |
dc.rights.spa.fl_str_mv |
Derechos reservados - Universidad Nacional de Colombia |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.license.spa.fl_str_mv |
Atribución-NoComercial 4.0 Internacional |
dc.rights.uri.spa.fl_str_mv |
http://creativecommons.org/licenses/by-nc/4.0/ |
dc.rights.accessrights.spa.fl_str_mv |
info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Atribución-NoComercial 4.0 Internacional Derechos reservados - Universidad Nacional de Colombia http://creativecommons.org/licenses/by-nc/4.0/ http://purl.org/coar/access_right/c_abf2 |
eu_rights_str_mv |
openAccess |
dc.format.mimetype.spa.fl_str_mv |
application/pdf |
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Universidad Nacional de Colombia - Sede Bogotá - Facultad de Medicina |
institution |
Universidad Nacional de Colombia |
bitstream.url.fl_str_mv |
https://repositorio.unal.edu.co/bitstream/unal/65187/1/50475-315029-1-PB.pdf https://repositorio.unal.edu.co/bitstream/unal/65187/2/50475-315029-1-PB.pdf.jpg |
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MD5 MD5 |
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Repositorio Institucional Universidad Nacional de Colombia |
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repositorio_nal@unal.edu.co |
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1814089485090029568 |
spelling |
Atribución-NoComercial 4.0 InternacionalDerechos reservados - Universidad Nacional de Colombiahttp://creativecommons.org/licenses/by-nc/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Barros, Gisela85dc25e7-3d51-4d22-a91b-a5ef372be0a1300Trujillo, Angela María1dc15837-7261-4c28-b8d4-c9c82e1bcec7300Jaramillo, Lina11561f78-1efd-448a-a965-8dc1c75a9e5c300Ortiz, Francy Helena95d0b960-859b-497a-946b-520f3cdc03c5300Contreras, Agustin Dariod71e9654-0d41-4a6e-bfe0-7e7df9458b943002019-07-02T23:57:30Z2019-07-02T23:57:30Z2016-07-01ISSN: 2357-3848https://repositorio.unal.edu.co/handle/unal/65187http://bdigital.unal.edu.co/66210/Background: Osteosarcoma (OS) and Ewing’s Sarcoma (ES) are the two most common malignant bone tumors in children. A retrospective review of the records of children diagnosed in a pediatric hospital over a five year period (2008-2013) was performed.Objective: To present the experiences acquired during the treatment of these types of tumors and to compare the results obtained with those reported in the literature.Methodology: The database of the Oncology and Pathology Service of Fundación Hospital de la Misericordia (HOMI) was reviewed to identify patients with primary bone tumors referred for histopathology analysis.Results: 22 patients were diagnosed with OS, with a mean age of 11.9 years. 96% of cases were located in the lower extremities. All patients received neoadjuvant chemotherapy and 86% underwent surgical treatment; 13% survived. 15 patients were diagnosed with ES, with a mean age of 12.4 years. 67% of cases were located in flat bones, 53% of patients had metastasis when diagnosed, and all received neoadjuvant chemotherapy. 40% of patients received surgical intervention and 20% received radiotherapy. Survival at the completion of the reseearch was 33%.Conclusions: Cure and survival rates are lower than those reported in the literature despite efforts to improve treatments.Introducción. El osteosarcoma (OS) y el sarcoma de Ewing (SE) son los tumores óseos malignos más frecuentes en edad pediátrica. En el presente estudio se realiza la revisión de los tumores malignos primarios de hueso diagnosticados en un hospital pediátrico de referencia en un período de cinco años (2008-2013).Objetivos. Mostrar la experiencia en el tratamiento de osteosarcomas y sarcomas de Ewing y comparar los resultados con lo reportado en la literatura.Materiales y métodos. Se revisó la base de datos del Servicio de Oncología y Patología de la Fundación Hospital de la Misericordia (HOMI) para identificar los pacientes con tumores primarios de hueso remitidos para estudio histopatológico.Resultados. 22 pacientes con edad promedio de 11.9 años tuvieron diagnóstico de OS; 96% de los casos se localizaron en la extremidad inferior, 100% de los pacientes recibieron quimioterapia neoadyuvante, 86% recibieron manejo quirúrgico y 13% sobrevivieron. 15 pacientes con edad promedio de 12.4 años tuvieron diagnóstico de SE; 67% de los casos se localizaron en huesos planos, 53% de los pacientes presentaron metástasis al diagnóstico, 100% recibieron quimioterapia neoadyuvante, 40% fueron llevados a cirugía y 20% recibieron radioterapia. La sobrevida fue de 33% al finalizar esta investigación.Conclusiones. Las tasas de curación y sobrevida son menores a las reportadas en la literatura a pesar de esfuerzos en mejorar los tratamientos.application/pdfspaUniversidad Nacional de Colombia - Sede Bogotá - Facultad de Medicinahttps://revistas.unal.edu.co/index.php/revfacmed/article/view/50475Universidad Nacional de Colombia Revistas electrónicas UN Revista de la Facultad de MedicinaRevista de la Facultad de MedicinaBarros, Gisela and Trujillo, Angela María and Jaramillo, Lina and Ortiz, Francy Helena and Contreras, Agustin Dario (2016) Malignant bone tumors in Pediatrics. Five year experience in a pediatric referral center. Revista de la Facultad de Medicina, 64 (3). pp. 403-407. ISSN 2357-384861 Ciencias médicas; Medicina / Medicine and healthOsteosarcomaEwing’s SarcomaDisease ProgressionRecurrenceNeoplasm MetastasisOsteosarcomaSarcoma de EwingProgresión de la enfermedadRecurrenciaMetástasis de la neoplasiaMalignant bone tumors in Pediatrics. Five year experience in a pediatric referral centerArtículo de revistainfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1http://purl.org/coar/version/c_970fb48d4fbd8a85Texthttp://purl.org/redcol/resource_type/ARTORIGINAL50475-315029-1-PB.pdfapplication/pdf473925https://repositorio.unal.edu.co/bitstream/unal/65187/1/50475-315029-1-PB.pdf7ccb69edb571672777725cd8e6bfaf8dMD51THUMBNAIL50475-315029-1-PB.pdf.jpg50475-315029-1-PB.pdf.jpgGenerated Thumbnailimage/jpeg8479https://repositorio.unal.edu.co/bitstream/unal/65187/2/50475-315029-1-PB.pdf.jpgdd56763cbc7ba51d44beaf94bb3d1698MD52unal/65187oai:repositorio.unal.edu.co:unal/651872024-05-09 23:09:04.928Repositorio Institucional Universidad Nacional de Colombiarepositorio_nal@unal.edu.co |