Boundaries of a Systemic Disease: a Protean Presentation of Giant Cell Arteritis
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.17/3926 |
Resumo: | A 60-year-old man was hospitalised with persistent fever, arm pain, dry cough and cholestasis. Diagnostic workup was remarkable for elevated inflammatory markers. Infectious diseases and autoimmune screening were negative. Imaging modalities excluded a neoplastic aetiology. Liver biopsy was negative for granulomatous or lymphomatous infiltrations. Giant cell arteritis (GCA) was suspected, but temporal artery Doppler ultrasound and biopsy were non-diagnostic. A positron emission tomography scan showed intense metabolic uptake in large vessels suggesting the diagnosis of GCA. Prednisolone was initiated with clinical and analytical improvement. At 1-year follow-up, there were no relapses and the patient remains symptom free. |
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Boundaries of a Systemic Disease: a Protean Presentation of Giant Cell ArteritisHSAC MEDMaleHumansMiddle AgedAnti-Inflammatory Agents, Non-SteroidalAspirin / therapeutic use*CholestasisCoughDiagnosis, DifferentialDrug Therapy, CombinationFever of Unknown OriginGiant Cell Arteritis / diagnostic imaging*Giant Cell Arteritis / drug therapy*Glucocorticoids / therapeutic usePositron-Emission TomographyPrednisolone / therapeutic use*A 60-year-old man was hospitalised with persistent fever, arm pain, dry cough and cholestasis. Diagnostic workup was remarkable for elevated inflammatory markers. Infectious diseases and autoimmune screening were negative. Imaging modalities excluded a neoplastic aetiology. Liver biopsy was negative for granulomatous or lymphomatous infiltrations. Giant cell arteritis (GCA) was suspected, but temporal artery Doppler ultrasound and biopsy were non-diagnostic. A positron emission tomography scan showed intense metabolic uptake in large vessels suggesting the diagnosis of GCA. Prednisolone was initiated with clinical and analytical improvement. At 1-year follow-up, there were no relapses and the patient remains symptom free.BMJRepositório do Centro Hospitalar Universitário de Lisboa Central, EPEMesquita, ACamara, LPatrício, CBrotas, V2021-11-24T16:23:34Z20202020-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/3926engBMJ Case Rep. 2020 Mar 25;13(3):e232234.10.1136/bcr-2019-232234.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-10T09:44:38Zoai:repositorio.chlc.min-saude.pt:10400.17/3926Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:21:14.098776Repositório 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 |
Boundaries of a Systemic Disease: a Protean Presentation of Giant Cell Arteritis |
title |
Boundaries of a Systemic Disease: a Protean Presentation of Giant Cell Arteritis |
spellingShingle |
Boundaries of a Systemic Disease: a Protean Presentation of Giant Cell Arteritis Mesquita, A HSAC MED Male Humans Middle Aged Anti-Inflammatory Agents, Non-Steroidal Aspirin / therapeutic use* Cholestasis Cough Diagnosis, Differential Drug Therapy, Combination Fever of Unknown Origin Giant Cell Arteritis / diagnostic imaging* Giant Cell Arteritis / drug therapy* Glucocorticoids / therapeutic use Positron-Emission Tomography Prednisolone / therapeutic use* |
title_short |
Boundaries of a Systemic Disease: a Protean Presentation of Giant Cell Arteritis |
title_full |
Boundaries of a Systemic Disease: a Protean Presentation of Giant Cell Arteritis |
title_fullStr |
Boundaries of a Systemic Disease: a Protean Presentation of Giant Cell Arteritis |
title_full_unstemmed |
Boundaries of a Systemic Disease: a Protean Presentation of Giant Cell Arteritis |
title_sort |
Boundaries of a Systemic Disease: a Protean Presentation of Giant Cell Arteritis |
author |
Mesquita, A |
author_facet |
Mesquita, A Camara, L Patrício, C Brotas, V |
author_role |
author |
author2 |
Camara, L Patrício, C Brotas, V |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE |
dc.contributor.author.fl_str_mv |
Mesquita, A Camara, L Patrício, C Brotas, V |
dc.subject.por.fl_str_mv |
HSAC MED Male Humans Middle Aged Anti-Inflammatory Agents, Non-Steroidal Aspirin / therapeutic use* Cholestasis Cough Diagnosis, Differential Drug Therapy, Combination Fever of Unknown Origin Giant Cell Arteritis / diagnostic imaging* Giant Cell Arteritis / drug therapy* Glucocorticoids / therapeutic use Positron-Emission Tomography Prednisolone / therapeutic use* |
topic |
HSAC MED Male Humans Middle Aged Anti-Inflammatory Agents, Non-Steroidal Aspirin / therapeutic use* Cholestasis Cough Diagnosis, Differential Drug Therapy, Combination Fever of Unknown Origin Giant Cell Arteritis / diagnostic imaging* Giant Cell Arteritis / drug therapy* Glucocorticoids / therapeutic use Positron-Emission Tomography Prednisolone / therapeutic use* |
description |
A 60-year-old man was hospitalised with persistent fever, arm pain, dry cough and cholestasis. Diagnostic workup was remarkable for elevated inflammatory markers. Infectious diseases and autoimmune screening were negative. Imaging modalities excluded a neoplastic aetiology. Liver biopsy was negative for granulomatous or lymphomatous infiltrations. Giant cell arteritis (GCA) was suspected, but temporal artery Doppler ultrasound and biopsy were non-diagnostic. A positron emission tomography scan showed intense metabolic uptake in large vessels suggesting the diagnosis of GCA. Prednisolone was initiated with clinical and analytical improvement. At 1-year follow-up, there were no relapses and the patient remains symptom free. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020 2020-01-01T00:00:00Z 2021-11-24T16:23:34Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.17/3926 |
url |
http://hdl.handle.net/10400.17/3926 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
BMJ Case Rep. 2020 Mar 25;13(3):e232234. 10.1136/bcr-2019-232234. |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
BMJ |
publisher.none.fl_str_mv |
BMJ |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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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 |
repository.mail.fl_str_mv |
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1799131308422594560 |