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Parosteal osteosarcoma mimicking osteochondroma: A radio-histologic approach on two cases

OBJECTIVE: Parosteal osteosarcoma is a well-differentiated variant of osteosarcoma that affects the surface of the bone. The imaging pattern is very typical. We report two cases mimicking an osteochondroma, radiologically and histologically and propose an explanation. MATERIAL: The review of 86 paro...

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Autores principales: Papathanassiou, Zafiria G, Alberghini, Marco, Thiesse, Philippe, Gambarotti, Marco, Bianchi, Giuseppe, Tranfaglia, Cristina, Vanel, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3372285/
https://www.ncbi.nlm.nih.gov/pubmed/22613734
http://dx.doi.org/10.1186/2045-3329-1-2
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author Papathanassiou, Zafiria G
Alberghini, Marco
Thiesse, Philippe
Gambarotti, Marco
Bianchi, Giuseppe
Tranfaglia, Cristina
Vanel, Daniel
author_facet Papathanassiou, Zafiria G
Alberghini, Marco
Thiesse, Philippe
Gambarotti, Marco
Bianchi, Giuseppe
Tranfaglia, Cristina
Vanel, Daniel
author_sort Papathanassiou, Zafiria G
collection PubMed
description OBJECTIVE: Parosteal osteosarcoma is a well-differentiated variant of osteosarcoma that affects the surface of the bone. The imaging pattern is very typical. We report two cases mimicking an osteochondroma, radiologically and histologically and propose an explanation. MATERIAL: The review of 86 parosteal osteosarcomas of bone revealed this atypical pattern only once. A consultation case was received in the same time, and added to ours. Patients were 28 years old and 56 years old females. Imaging studies included two radiographs, two CTscans, one MRI examination and one bone scan and the results were compared to histology. RESULTS: On imaging, both lesions presented as ossified lobulated masses attached with a broad base to the underlying cortex. No radiolucent cleft separated the masses and the host bone and cortex continuity between the mass and the femur was seen, with medullary communication. The marrow of the mass had a different density and intensity compared to normal marrow. So, there were features of an osteochondroma (cortex and medullary continuity) and of a parosteal osteosarcoma (ossified marrow). Pathological assessment on the final specimen confirmed the presence of low-grade parosteal osteosarcomas, after an erroneous diagnosis of osteochondroma on the initial biopsy. CONCLUSIONS: Parosteal osteosarcoma can be rarely confused with osteochondroma. A radiologic-pathologic correlation is essential. Cortex continuity is the most misleading imaging feature that may occur in parosteal osteosarcomas. A knowledge of this misleading pattern will help diagnose the lesion from the beginning.
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spelling pubmed-33722852012-06-12 Parosteal osteosarcoma mimicking osteochondroma: A radio-histologic approach on two cases Papathanassiou, Zafiria G Alberghini, Marco Thiesse, Philippe Gambarotti, Marco Bianchi, Giuseppe Tranfaglia, Cristina Vanel, Daniel Clin Sarcoma Res Research OBJECTIVE: Parosteal osteosarcoma is a well-differentiated variant of osteosarcoma that affects the surface of the bone. The imaging pattern is very typical. We report two cases mimicking an osteochondroma, radiologically and histologically and propose an explanation. MATERIAL: The review of 86 parosteal osteosarcomas of bone revealed this atypical pattern only once. A consultation case was received in the same time, and added to ours. Patients were 28 years old and 56 years old females. Imaging studies included two radiographs, two CTscans, one MRI examination and one bone scan and the results were compared to histology. RESULTS: On imaging, both lesions presented as ossified lobulated masses attached with a broad base to the underlying cortex. No radiolucent cleft separated the masses and the host bone and cortex continuity between the mass and the femur was seen, with medullary communication. The marrow of the mass had a different density and intensity compared to normal marrow. So, there were features of an osteochondroma (cortex and medullary continuity) and of a parosteal osteosarcoma (ossified marrow). Pathological assessment on the final specimen confirmed the presence of low-grade parosteal osteosarcomas, after an erroneous diagnosis of osteochondroma on the initial biopsy. CONCLUSIONS: Parosteal osteosarcoma can be rarely confused with osteochondroma. A radiologic-pathologic correlation is essential. Cortex continuity is the most misleading imaging feature that may occur in parosteal osteosarcomas. A knowledge of this misleading pattern will help diagnose the lesion from the beginning. BioMed Central 2011-07-25 /pmc/articles/PMC3372285/ /pubmed/22613734 http://dx.doi.org/10.1186/2045-3329-1-2 Text en Copyright ©2011 Papathanassiou et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Papathanassiou, Zafiria G
Alberghini, Marco
Thiesse, Philippe
Gambarotti, Marco
Bianchi, Giuseppe
Tranfaglia, Cristina
Vanel, Daniel
Parosteal osteosarcoma mimicking osteochondroma: A radio-histologic approach on two cases
title Parosteal osteosarcoma mimicking osteochondroma: A radio-histologic approach on two cases
title_full Parosteal osteosarcoma mimicking osteochondroma: A radio-histologic approach on two cases
title_fullStr Parosteal osteosarcoma mimicking osteochondroma: A radio-histologic approach on two cases
title_full_unstemmed Parosteal osteosarcoma mimicking osteochondroma: A radio-histologic approach on two cases
title_short Parosteal osteosarcoma mimicking osteochondroma: A radio-histologic approach on two cases
title_sort parosteal osteosarcoma mimicking osteochondroma: a radio-histologic approach on two cases
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3372285/
https://www.ncbi.nlm.nih.gov/pubmed/22613734
http://dx.doi.org/10.1186/2045-3329-1-2
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