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...

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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
id UNACIONAL2_eaecdf78895f1d1eafd9df1563e03f10
oai_identifier_str oai:repositorio.unal.edu.co:unal/65187
network_acronym_str UNACIONAL2
network_name_str Universidad Nacional de Colombia
repository_id_str
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
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dc.type.content.spa.fl_str_mv Text
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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
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identifier_str_mv ISSN: 2357-3848
url https://repositorio.unal.edu.co/handle/unal/65187
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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
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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
dc.publisher.spa.fl_str_mv 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
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repository.name.fl_str_mv Repositorio Institucional Universidad Nacional de Colombia
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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