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Periosteal osteoblastoma: Multimodal imaging of a rare neoplasm

Osteoblastoma is a rare neoplasm, accounting for only 1% of the primary bone neoplasms. We report a case of periosteal osteoblastoma, a rare subtype of osteoblastoma. To the best of our knowledge, only 30 cases of periosteal osteoblastoma appear in the English literature. Our case is that of a 41-ye...

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Detalles Bibliográficos
Autores principales: Sharma, Vipul, Chew, Felix S., Hoch, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898178/
https://www.ncbi.nlm.nih.gov/pubmed/27307837
http://dx.doi.org/10.2484/rcr.v4i4.329
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author Sharma, Vipul
Chew, Felix S.
Hoch, Benjamin
author_facet Sharma, Vipul
Chew, Felix S.
Hoch, Benjamin
author_sort Sharma, Vipul
collection PubMed
description Osteoblastoma is a rare neoplasm, accounting for only 1% of the primary bone neoplasms. We report a case of periosteal osteoblastoma, a rare subtype of osteoblastoma. To the best of our knowledge, only 30 cases of periosteal osteoblastoma appear in the English literature. Our case is that of a 41-year-old male with vague intermittent knee pain over a two-year period. Diagnostic imaging revealed an aggressive-appearing lesion in the posterior distal femur, which was initially considered to be a surface osteosarcoma. Roentgenographic, CT, MRI, and bone scan features are presented.
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spelling pubmed-48981782016-06-15 Periosteal osteoblastoma: Multimodal imaging of a rare neoplasm Sharma, Vipul Chew, Felix S. Hoch, Benjamin Radiol Case Rep Article Osteoblastoma is a rare neoplasm, accounting for only 1% of the primary bone neoplasms. We report a case of periosteal osteoblastoma, a rare subtype of osteoblastoma. To the best of our knowledge, only 30 cases of periosteal osteoblastoma appear in the English literature. Our case is that of a 41-year-old male with vague intermittent knee pain over a two-year period. Diagnostic imaging revealed an aggressive-appearing lesion in the posterior distal femur, which was initially considered to be a surface osteosarcoma. Roentgenographic, CT, MRI, and bone scan features are presented. Elsevier 2015-11-06 /pmc/articles/PMC4898178/ /pubmed/27307837 http://dx.doi.org/10.2484/rcr.v4i4.329 Text en © 2009 The Authors. 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 Article
Sharma, Vipul
Chew, Felix S.
Hoch, Benjamin
Periosteal osteoblastoma: Multimodal imaging of a rare neoplasm
title Periosteal osteoblastoma: Multimodal imaging of a rare neoplasm
title_full Periosteal osteoblastoma: Multimodal imaging of a rare neoplasm
title_fullStr Periosteal osteoblastoma: Multimodal imaging of a rare neoplasm
title_full_unstemmed Periosteal osteoblastoma: Multimodal imaging of a rare neoplasm
title_short Periosteal osteoblastoma: Multimodal imaging of a rare neoplasm
title_sort periosteal osteoblastoma: multimodal imaging of a rare neoplasm
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4898178/
https://www.ncbi.nlm.nih.gov/pubmed/27307837
http://dx.doi.org/10.2484/rcr.v4i4.329
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