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A rare benign disorder mimicking metastasis on radiographic examination: a case report of osteopoikilosis

Osteopoikilosis (OPK) is a rare, autosomal dominant bone disorder, characterized by multiple, discrete round or ovoid radio densities scattered throughout the axial and appendicular skeleton. OPK is usually asymptomatic but rarely there may be slight articular pain and joint effusions. OPK is genera...

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Autores principales: Ozdemirel, Ali Erhan, Cakit, Burcu Duyur, Erdem, Hatice Rana, Koc, Bunyamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141847/
https://www.ncbi.nlm.nih.gov/pubmed/21120491
http://dx.doi.org/10.1007/s00296-010-1664-2
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author Ozdemirel, Ali Erhan
Cakit, Burcu Duyur
Erdem, Hatice Rana
Koc, Bunyamin
author_facet Ozdemirel, Ali Erhan
Cakit, Burcu Duyur
Erdem, Hatice Rana
Koc, Bunyamin
author_sort Ozdemirel, Ali Erhan
collection PubMed
description Osteopoikilosis (OPK) is a rare, autosomal dominant bone disorder, characterized by multiple, discrete round or ovoid radio densities scattered throughout the axial and appendicular skeleton. OPK is usually asymptomatic but rarely there may be slight articular pain and joint effusions. OPK is generally diagnosed incidentally on radiographic examinations and may mimic different bone pathologies, including bone metastases. Radionuclide bone scan has a critical role in distinguishing OPK from osteoblastic bone metastases. In this case report, we present a young man with right hip pain due to OPK, whose plain radiogram and computerized tomography findings thought cancer metastasis.
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spelling pubmed-31418472011-09-08 A rare benign disorder mimicking metastasis on radiographic examination: a case report of osteopoikilosis Ozdemirel, Ali Erhan Cakit, Burcu Duyur Erdem, Hatice Rana Koc, Bunyamin Rheumatol Int Short Communication Osteopoikilosis (OPK) is a rare, autosomal dominant bone disorder, characterized by multiple, discrete round or ovoid radio densities scattered throughout the axial and appendicular skeleton. OPK is usually asymptomatic but rarely there may be slight articular pain and joint effusions. OPK is generally diagnosed incidentally on radiographic examinations and may mimic different bone pathologies, including bone metastases. Radionuclide bone scan has a critical role in distinguishing OPK from osteoblastic bone metastases. In this case report, we present a young man with right hip pain due to OPK, whose plain radiogram and computerized tomography findings thought cancer metastasis. Springer-Verlag 2010-12-01 2011 /pmc/articles/PMC3141847/ /pubmed/21120491 http://dx.doi.org/10.1007/s00296-010-1664-2 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Short Communication
Ozdemirel, Ali Erhan
Cakit, Burcu Duyur
Erdem, Hatice Rana
Koc, Bunyamin
A rare benign disorder mimicking metastasis on radiographic examination: a case report of osteopoikilosis
title A rare benign disorder mimicking metastasis on radiographic examination: a case report of osteopoikilosis
title_full A rare benign disorder mimicking metastasis on radiographic examination: a case report of osteopoikilosis
title_fullStr A rare benign disorder mimicking metastasis on radiographic examination: a case report of osteopoikilosis
title_full_unstemmed A rare benign disorder mimicking metastasis on radiographic examination: a case report of osteopoikilosis
title_short A rare benign disorder mimicking metastasis on radiographic examination: a case report of osteopoikilosis
title_sort rare benign disorder mimicking metastasis on radiographic examination: a case report of osteopoikilosis
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141847/
https://www.ncbi.nlm.nih.gov/pubmed/21120491
http://dx.doi.org/10.1007/s00296-010-1664-2
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