A Rare Case of Paget Disease
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , |
Tipo de documento: | Relatório |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://scielo.pt/scielo.php?script=sci_arttext&pid=S2183-13512023000100030 |
Resumo: | Abstract Paget disease is a skeletal disorder of unknown aetiology, characterised by excessive abnormal bone remodelling. It can be polyostotic, when two or more bones are involved or monostotic when only one bone is affected. We report the case of a patient admitted to our hospital who, on physical examination, presented an exuberant right clavicular mass. Imaging studies were performed and the diagnosis of Paget disease of the clavicle was made - an atypical and rare location of the disease. As Paget disease might be discovered incidentally, it is crucial to be familiar with its typical radiographic appearance to avoid misinterpretation. |
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7160 |
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A Rare Case of Paget DiseasePaget diseaseclavicle.Abstract Paget disease is a skeletal disorder of unknown aetiology, characterised by excessive abnormal bone remodelling. It can be polyostotic, when two or more bones are involved or monostotic when only one bone is affected. We report the case of a patient admitted to our hospital who, on physical examination, presented an exuberant right clavicular mass. Imaging studies were performed and the diagnosis of Paget disease of the clavicle was made - an atypical and rare location of the disease. As Paget disease might be discovered incidentally, it is crucial to be familiar with its typical radiographic appearance to avoid misinterpretation.Sociedade Portuguesa de Radiologia e Medicina Nuclear2023-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/reporttext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S2183-13512023000100030Acta Radiológica Portuguesa v.35 n.1 2023reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttp://scielo.pt/scielo.php?script=sci_arttext&pid=S2183-13512023000100030Rodrigues,Maria InêsDourado,JoãoPereira,Bárbara RibeiroCosta,Francisco RegoMadureira,Antónioinfo:eu-repo/semantics/openAccess2024-02-06T17:29:32Zoai:scielo:S2183-13512023000100030Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:33:25.835159Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
A Rare Case of Paget Disease |
title |
A Rare Case of Paget Disease |
spellingShingle |
A Rare Case of Paget Disease Rodrigues,Maria Inês Paget disease clavicle. |
title_short |
A Rare Case of Paget Disease |
title_full |
A Rare Case of Paget Disease |
title_fullStr |
A Rare Case of Paget Disease |
title_full_unstemmed |
A Rare Case of Paget Disease |
title_sort |
A Rare Case of Paget Disease |
author |
Rodrigues,Maria Inês |
author_facet |
Rodrigues,Maria Inês Dourado,João Pereira,Bárbara Ribeiro Costa,Francisco Rego Madureira,António |
author_role |
author |
author2 |
Dourado,João Pereira,Bárbara Ribeiro Costa,Francisco Rego Madureira,António |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Rodrigues,Maria Inês Dourado,João Pereira,Bárbara Ribeiro Costa,Francisco Rego Madureira,António |
dc.subject.por.fl_str_mv |
Paget disease clavicle. |
topic |
Paget disease clavicle. |
description |
Abstract Paget disease is a skeletal disorder of unknown aetiology, characterised by excessive abnormal bone remodelling. It can be polyostotic, when two or more bones are involved or monostotic when only one bone is affected. We report the case of a patient admitted to our hospital who, on physical examination, presented an exuberant right clavicular mass. Imaging studies were performed and the diagnosis of Paget disease of the clavicle was made - an atypical and rare location of the disease. As Paget disease might be discovered incidentally, it is crucial to be familiar with its typical radiographic appearance to avoid misinterpretation. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-04-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/report |
format |
report |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://scielo.pt/scielo.php?script=sci_arttext&pid=S2183-13512023000100030 |
url |
http://scielo.pt/scielo.php?script=sci_arttext&pid=S2183-13512023000100030 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
http://scielo.pt/scielo.php?script=sci_arttext&pid=S2183-13512023000100030 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Portuguesa de Radiologia e Medicina Nuclear |
publisher.none.fl_str_mv |
Sociedade Portuguesa de Radiologia e Medicina Nuclear |
dc.source.none.fl_str_mv |
Acta Radiológica Portuguesa v.35 n.1 2023 reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799137393013424128 |