Synchronous multicentric osteosarcoma in a 15-year-old pediatric patient: case report
Main Article Content
Abstract
Background: Cancer in the pediatric population is between 2 to 3% of all malignant tumors. The most frequent tumors in children are leukemias (30%), brain tumors (20%), and lymphomas (15%). Bone tumors represent 6% of neoplasms in children; osteosarcoma constitutes 55% of cases, with a peak incidence at 15 years. This neoplasia has an aggressive behavior with metastasis of approximately 15% at the time of diagnosis, the lungs being the most frequent site followed by bone, lymph nodes, liver, and brain. When the diagnosis shows more than one bone lesion without visceral metastasis, the term multicentric and synchronous is added; this entity is of rare appearance, with a report of fewer than 100 cases in the literature. Case report: In the following case, we present a 15-year-old patient with disabling pain in the left lower limb and images suggestive of synchronous multicentric bone neoplasm and biopsy that concluded chondrogenic variant osteosarcoma. Conclusion: The patient received palliative cancer treatment and later presented pulmonary metastasis. This variant of osteosarcoma is extremely aggressive with a very poor prognosis.
Downloads
Article Details
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Creative Commons
License Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
You are free to:
Share - copy and redistribute the material in any medium or format.
Adapt - remix, transform, and build upon the material The licensor cannot revoke these freedoms as long as you follow the license terms.
• Attribution — You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.
• NonCommercial — You may not use the material for commercial purposes.
• ShareAlike — If you remix, transform, or build upon the material, you must distribute your contributions under the same license as the original.
• No additional restrictions — You may not apply legal terms or technological measures that legally restrict others from doing anything the license permits.
References
Longhi A, Anna Paioli, Emanuela Palmerini, Marilena Cesari, Massimo E. Abate, Elisabetta Setola, Paolo Spinnato, Davide Donati, Ivar Hompland & Kjetil Boye. Pazopanib in relapsed osteosarcoma patients: report on 15 cases. Acta Oncologica. 2019;(58)1:124-128. DOI: https://doi.org/10.1080/0284186X.2018.1503714
Mirabello L, Yeager M, Mai PL, Gastier-Foster JM, Gorlick R, Khanna C, et al. Germline TP53 Variants and Susceptibility to Osteosarcoma. J Natl Cancer Inst. 2015;107(7): djv101. DOI: https://doi.org/10.1093/jnci/djv101
Saeter G, Hoie J, Stenwig AE, Hannisdal E, Solheim P. Systemic relapse of patients with osteogenic sarcoma. Prognostic factors for long term survival. Cancer. 1995;75:1084-1089. DOI: https://doi.org/10.1002/1097-0142(19950301)75:5<1084::AID-CNCR2820750506>3.0.CO;2-F
Bielack SS, Kempf-Bielack B, Delling G. Prognostic factors in high-grade osteosarcoma of the extremities or trunk: an analysis of 1,702 patients treated on neoadjuvant cooperative osteosarcoma study group protocols.J Clin Oncol. 2002; 20(3):776-90. DOI: https://doi.org/10.1200/JCO.2002.20.3.776
Badilla C. Osteosarcoma. Revista Médica de Costa Rica y Centroamerica 2014; 71(611).
Bustamante J, Arenas-Siles D, Valcarcel-Valdivia S, Salazar-Salazar D, Arangoytia-Arias R, Huapaya-Huertas O. Osteosarcoma multicéntrico sincrónico en paciente pediátrico: reporte de un caso. Acta méd. Perú. 2018 ; 35(2):127-132. DOI: https://doi.org/10.35663/amp.2018.352.482
De Azevedo JWV, De Medeiros Fernández TAA, Fernández JVJ, De Azevedo JCV, Lanza DCF, Bezerra CM. Biology and pathogenesis of human osteosarcoma. Oncol Lett. 2020;19(2):1099-116. DOI: https://doi.org/10.3892/ol.2019.11229
Hameed S, Vijayan S, Naik M, Rao S. Multicentric osteosarcoma. Singapore Med J. 2012;53(10):e214-7.
Gerrand C, Athanasou N, Brennan B, Grimer R, Judson I, Morland B. UK guidelines for the management of bone sarcomas. Clin Sarcoma Res. 2016;6(1):7. DOI: https://doi.org/10.1186/s13569-016-0047-1
Pérez-García J, Velasco-Donado O, Roblés-Perez K. Osteosarcoma multicéntrico sincrónico. Un caso en niño de 10 años y revisión de la literatura. Rev Esp Patol. 2020;S11-S15. DOI: https://doi.org/10.1016/j.patol.2020.10.001
WHO Classification of tumours Editorial Board. Soft Tissue and Bone Tumours. Lyon (France): International Agency for Research on Cancer. 2020.
Rossier-Guillot LA, Tecualt-Gómez R, Amaya-Cepeda R, Barrera-García MI. Osteosarcoma multicéntrico sincrónico con múltiples tumores primarios o enfermedad metastásica: reporte de un caso y revisión de la literatura. Acta Ortop Mex. 2014;28:179-82.
Hatori M, Ohtani H, Yamada N, Uzuki M, Kokubun S. Synchronous multifocal osteosarcoma with lymphatic spread in the lung: an autopsy case report. Japanese Journal of Clinical Oncology. 2001;31(11):562-6. DOI: https://doi.org/10.1093/jjco/hye118
David Tarud, G., Ruiz Pérez, O., Sagbini Guerrero, E. & Segura Ramos, S. (2018). Hematología y Oncología Pediátrica. Barranquilla: Editorial Mejoras.
Bermúdez-Balbuena V, López-Durán A, Shalkow J, López-Marmolejo A, Isunza-Ramírez A. Osteosarcoma osteoblástico multicéntrico en un preescolar. Informe de caso. Acta Ortopédica Mexicana 2011; 25(4):232-235.