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Surface osteosarcoma: Clinical features and therapeutic implications

INTRODUCTION: Surface osteosarcoma are rare variant of osteosarcoma that include parosteal osteosarcoma, periosteal osteosarcoma and high grade surface osteosarcoma. These lesions have different clinical presentation and biological behavior compared to conventional osteosarcoma, and hence need to be...

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Autores principales: Nouri, H., Ben Maitigue, M., Abid, L., Nouri, N., Abdelkader, A., Bouaziz, M., Mestiri, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678793/
https://www.ncbi.nlm.nih.gov/pubmed/26730360
http://dx.doi.org/10.1016/j.jbo.2015.07.002
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author Nouri, H.
Ben Maitigue, M.
Abid, L.
Nouri, N.
Abdelkader, A.
Bouaziz, M.
Mestiri, M.
author_facet Nouri, H.
Ben Maitigue, M.
Abid, L.
Nouri, N.
Abdelkader, A.
Bouaziz, M.
Mestiri, M.
author_sort Nouri, H.
collection PubMed
description INTRODUCTION: Surface osteosarcoma are rare variant of osteosarcoma that include parosteal osteosarcoma, periosteal osteosarcoma and high grade surface osteosarcoma. These lesions have different clinical presentation and biological behavior compared to conventional osteosarcoma, and hence need to be managed differently. GOAL: The aim of this study is to analyze the clinico-pathological features and outcome of a series of surface osteosarcoma in an attempt to define the adequate treatment of this rare entity. PATIENT AND METHOD: It is a retrospective and bicentric study of 18 surface osteosarcoma that were seen at the KASSAB’s Institute and SAHLOUL Hospital from 2006 to 2013. The authors reviewed the clinical and radiologic features, histologic sections, treatments, and outcomes in this group of patients. RESULTS: Seven patients were male (38.9%) and 11 were female (61.1%) with mean age of 25 years (range from 16 to 55 years). Eleven lesions were in the femur and 7 in the tibia. We identified 11 parosteal osteosarcoma (six of them were dedifferentiated), 3 periosteal osteosarcoma and 4 high grade surface osteosarcoma. Six patients had neoadjuvant chemotherapy and all lesions had surgical resection. Margins were wide in 15 cases and intra lesional in 3 cases. Histological response to chemotherapy was poor in all cases. The mean follow up was 34.5 months. Six patients (33.3%) presented local recurrence and 8 patients (44.4%) presented lung metastases. Six patients (33.3%) died from the disease after a mean follow up of 12 months (6–30 months); all of them had high grade lesions. CONCLUSION: Histological grade of malignancy is the main point to assess in surface osteosarcoma since it determines treatment and prognosis. Low grade lesions should be treated by wide resection, while high grade lesions need more aggressive surgical approach associated to post operative chemotherapy.
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spelling pubmed-46787932016-01-04 Surface osteosarcoma: Clinical features and therapeutic implications Nouri, H. Ben Maitigue, M. Abid, L. Nouri, N. Abdelkader, A. Bouaziz, M. Mestiri, M. J Bone Oncol Research Paper INTRODUCTION: Surface osteosarcoma are rare variant of osteosarcoma that include parosteal osteosarcoma, periosteal osteosarcoma and high grade surface osteosarcoma. These lesions have different clinical presentation and biological behavior compared to conventional osteosarcoma, and hence need to be managed differently. GOAL: The aim of this study is to analyze the clinico-pathological features and outcome of a series of surface osteosarcoma in an attempt to define the adequate treatment of this rare entity. PATIENT AND METHOD: It is a retrospective and bicentric study of 18 surface osteosarcoma that were seen at the KASSAB’s Institute and SAHLOUL Hospital from 2006 to 2013. The authors reviewed the clinical and radiologic features, histologic sections, treatments, and outcomes in this group of patients. RESULTS: Seven patients were male (38.9%) and 11 were female (61.1%) with mean age of 25 years (range from 16 to 55 years). Eleven lesions were in the femur and 7 in the tibia. We identified 11 parosteal osteosarcoma (six of them were dedifferentiated), 3 periosteal osteosarcoma and 4 high grade surface osteosarcoma. Six patients had neoadjuvant chemotherapy and all lesions had surgical resection. Margins were wide in 15 cases and intra lesional in 3 cases. Histological response to chemotherapy was poor in all cases. The mean follow up was 34.5 months. Six patients (33.3%) presented local recurrence and 8 patients (44.4%) presented lung metastases. Six patients (33.3%) died from the disease after a mean follow up of 12 months (6–30 months); all of them had high grade lesions. CONCLUSION: Histological grade of malignancy is the main point to assess in surface osteosarcoma since it determines treatment and prognosis. Low grade lesions should be treated by wide resection, while high grade lesions need more aggressive surgical approach associated to post operative chemotherapy. Elsevier 2015-11-10 /pmc/articles/PMC4678793/ /pubmed/26730360 http://dx.doi.org/10.1016/j.jbo.2015.07.002 Text en © 2015 Published by Elsevier GmbH. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Nouri, H.
Ben Maitigue, M.
Abid, L.
Nouri, N.
Abdelkader, A.
Bouaziz, M.
Mestiri, M.
Surface osteosarcoma: Clinical features and therapeutic implications
title Surface osteosarcoma: Clinical features and therapeutic implications
title_full Surface osteosarcoma: Clinical features and therapeutic implications
title_fullStr Surface osteosarcoma: Clinical features and therapeutic implications
title_full_unstemmed Surface osteosarcoma: Clinical features and therapeutic implications
title_short Surface osteosarcoma: Clinical features and therapeutic implications
title_sort surface osteosarcoma: clinical features and therapeutic implications
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4678793/
https://www.ncbi.nlm.nih.gov/pubmed/26730360
http://dx.doi.org/10.1016/j.jbo.2015.07.002
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