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Bifocal parosteal osteoma of femur: A case report and review of literature

Osteoma is a benign, slowly growing, asymptomatic, bone-forming tumor arising from cancellous or compact bone. Osteoma usually is a solitary lesion, but in patients with Gardner’s Syndrome it may be multiple. osteoma may rarely have a parosteal localization. Parosteal osteoma has peculiar radiograph...

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Autores principales: Vitiello, Raffaele, Greco, Tommaso, Cianni, Luigi, Careri, Silvia, Oliva, Maria Serena, Gessi, Marco, De Martino, Ivan, Bocchi, Maria Beatrice, Maccauro, Giulio, Perisano, Carlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459375/
https://www.ncbi.nlm.nih.gov/pubmed/32913604
http://dx.doi.org/10.4081/or.2020.8673
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author Vitiello, Raffaele
Greco, Tommaso
Cianni, Luigi
Careri, Silvia
Oliva, Maria Serena
Gessi, Marco
De Martino, Ivan
Bocchi, Maria Beatrice
Maccauro, Giulio
Perisano, Carlo
author_facet Vitiello, Raffaele
Greco, Tommaso
Cianni, Luigi
Careri, Silvia
Oliva, Maria Serena
Gessi, Marco
De Martino, Ivan
Bocchi, Maria Beatrice
Maccauro, Giulio
Perisano, Carlo
author_sort Vitiello, Raffaele
collection PubMed
description Osteoma is a benign, slowly growing, asymptomatic, bone-forming tumor arising from cancellous or compact bone. Osteoma usually is a solitary lesion, but in patients with Gardner’s Syndrome it may be multiple. osteoma may rarely have a parosteal localization. Parosteal osteoma has peculiar radiographic, histologic and clinical features. We describe a case report of a 51- years old man with a bifocal parosteal osteoma of the femur in a non-syndromic patient. This is the first described patient with a bifocal lesion. In literature only 24 cases of paraosteal osteoma are found. Our patient underwent surgery and the lesions were fully excised. At one year follow-up there was no evidence of recurrence.
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spelling pubmed-74593752020-09-09 Bifocal parosteal osteoma of femur: A case report and review of literature Vitiello, Raffaele Greco, Tommaso Cianni, Luigi Careri, Silvia Oliva, Maria Serena Gessi, Marco De Martino, Ivan Bocchi, Maria Beatrice Maccauro, Giulio Perisano, Carlo Orthop Rev (Pavia) Case Report Osteoma is a benign, slowly growing, asymptomatic, bone-forming tumor arising from cancellous or compact bone. Osteoma usually is a solitary lesion, but in patients with Gardner’s Syndrome it may be multiple. osteoma may rarely have a parosteal localization. Parosteal osteoma has peculiar radiographic, histologic and clinical features. We describe a case report of a 51- years old man with a bifocal parosteal osteoma of the femur in a non-syndromic patient. This is the first described patient with a bifocal lesion. In literature only 24 cases of paraosteal osteoma are found. Our patient underwent surgery and the lesions were fully excised. At one year follow-up there was no evidence of recurrence. PAGEPress Publications, Pavia, Italy 2020-06-25 /pmc/articles/PMC7459375/ /pubmed/32913604 http://dx.doi.org/10.4081/or.2020.8673 Text en ©Copyright: the Author(s) http://creativecommons.org/licenses/by-nc/4.0/ This work is licensed under a Creative Commons Attribution NonCommercial 4.0 License (CC BY-NC 4.0).
spellingShingle Case Report
Vitiello, Raffaele
Greco, Tommaso
Cianni, Luigi
Careri, Silvia
Oliva, Maria Serena
Gessi, Marco
De Martino, Ivan
Bocchi, Maria Beatrice
Maccauro, Giulio
Perisano, Carlo
Bifocal parosteal osteoma of femur: A case report and review of literature
title Bifocal parosteal osteoma of femur: A case report and review of literature
title_full Bifocal parosteal osteoma of femur: A case report and review of literature
title_fullStr Bifocal parosteal osteoma of femur: A case report and review of literature
title_full_unstemmed Bifocal parosteal osteoma of femur: A case report and review of literature
title_short Bifocal parosteal osteoma of femur: A case report and review of literature
title_sort bifocal parosteal osteoma of femur: a case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459375/
https://www.ncbi.nlm.nih.gov/pubmed/32913604
http://dx.doi.org/10.4081/or.2020.8673
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