Sarcoidosis – case report

Detalhes bibliográficos
Autor(a) principal: Magalhães, S.
Data de Publicação: 2009
Outros Autores: Bessa, I., Guedes, F.
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://revista.spmi.pt/index.php/rpmi/article/view/1433
Resumo: Sarcoidosis is a multisystem granulomatous disorder of unknown cause that presents most frequently in young adults with bilateral hilar adenopathy and pulmonary infiltrates.Although the disease spontaneously resolve in many patients, may also take a progressive and severe outcome. The lack of markers of activity and prognosis, and the lack of treatment protocols, raise many doubts on the decision to treat and to provide optimum therapy to the patient.We present a 32 year old female patient, which is followed for 10 years with the diagnosis of sarcoidosis, initially with lung and lymph node involvement.Despite the good initial response to steroid therapy, the disease appears to be steroid-dependent and progressive, with multisystemic involvement. The steroids side-effects and the inefficiency of azathioprine as “steroid sparing agent” contribute to the difficulty in monitoring the progression of the disease.Given the unfavourable progression of sarcoidosis and the desire expressed by the patient to become pregnant, we present this case as a model of the challenges posed by this disease.
id RCAP_eba57502ff252ec52f59a5b9efb44a8c
oai_identifier_str oai:oai.revista.spmi.pt:article/1433
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling Sarcoidosis – case reportSarcoidose – caso clínicosarcoidosefibrose pulmonargravidezsarcoidosispulmonary fibrosispregnancySarcoidosis is a multisystem granulomatous disorder of unknown cause that presents most frequently in young adults with bilateral hilar adenopathy and pulmonary infiltrates.Although the disease spontaneously resolve in many patients, may also take a progressive and severe outcome. The lack of markers of activity and prognosis, and the lack of treatment protocols, raise many doubts on the decision to treat and to provide optimum therapy to the patient.We present a 32 year old female patient, which is followed for 10 years with the diagnosis of sarcoidosis, initially with lung and lymph node involvement.Despite the good initial response to steroid therapy, the disease appears to be steroid-dependent and progressive, with multisystemic involvement. The steroids side-effects and the inefficiency of azathioprine as “steroid sparing agent” contribute to the difficulty in monitoring the progression of the disease.Given the unfavourable progression of sarcoidosis and the desire expressed by the patient to become pregnant, we present this case as a model of the challenges posed by this disease.A sarcoidose é uma doença multissistémica granulomatosa de causa desconhecida, que ocorre frequentemente em adultos jovens e que se apresenta habitualmente com adenopatias hilares bilaterais e infiltrados pulmonares. Apesar de a doença resolver espontaneamente em muitos doentes, pode também assumir uma forma progressiva e severa. A ausência de marcadores de actividade e de prognóstico, bem como a inexistência de protocolos de tratamento suscitam muitas dúvidas na decisão de tratar e na terapêutica óptima a oferecer ao doente.Apresenta-se o caso clínico de uma doente do sexo feminino, de 32 anos de idade, que é seguida em consulta de Medicina há 10 anos, com o diagnóstico de sarcoidose, inicialmente com envolvimento pulmonar e ganglionar. Apesar da boa resposta inicial à terapêutica com corticóides, a doença revela-se corticodependente e progressiva, com atingimento multissistémico. A iatrogenia dos esteróides e a ineficácia da azatioprina como steroid sparing agent contribuem paralelamente para a dificuldade no controlo da progressão da doença.Dada a progressão desfavorável da sarcoidose e ao desejo de gravidez manifestado pela doente, apresentamos este caso clínico como reflexão dos desafios colocados por esta patologia.Sociedade Portuguesa de Medicina Interna2009-12-31info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://revista.spmi.pt/index.php/rpmi/article/view/1433Internal Medicine; Vol. 16 No. 4 (2009): Outubro/ Dezembro; 247-252Medicina Interna; Vol. 16 N.º 4 (2009): Outubro/ Dezembro; 247-2522183-99800872-671Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://revista.spmi.pt/index.php/rpmi/article/view/1433https://revista.spmi.pt/index.php/rpmi/article/view/1433/984Magalhães, S.Bessa, I.Guedes, F.info:eu-repo/semantics/openAccess2022-12-31T06:12:07Zoai:oai.revista.spmi.pt:article/1433Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:29:12.061497Repositório 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 Sarcoidosis – case report
Sarcoidose – caso clínico
title Sarcoidosis – case report
spellingShingle Sarcoidosis – case report
Magalhães, S.
sarcoidose
fibrose pulmonar
gravidez
sarcoidosis
pulmonary fibrosis
pregnancy
title_short Sarcoidosis – case report
title_full Sarcoidosis – case report
title_fullStr Sarcoidosis – case report
title_full_unstemmed Sarcoidosis – case report
title_sort Sarcoidosis – case report
author Magalhães, S.
author_facet Magalhães, S.
Bessa, I.
Guedes, F.
author_role author
author2 Bessa, I.
Guedes, F.
author2_role author
author
dc.contributor.author.fl_str_mv Magalhães, S.
Bessa, I.
Guedes, F.
dc.subject.por.fl_str_mv sarcoidose
fibrose pulmonar
gravidez
sarcoidosis
pulmonary fibrosis
pregnancy
topic sarcoidose
fibrose pulmonar
gravidez
sarcoidosis
pulmonary fibrosis
pregnancy
description Sarcoidosis is a multisystem granulomatous disorder of unknown cause that presents most frequently in young adults with bilateral hilar adenopathy and pulmonary infiltrates.Although the disease spontaneously resolve in many patients, may also take a progressive and severe outcome. The lack of markers of activity and prognosis, and the lack of treatment protocols, raise many doubts on the decision to treat and to provide optimum therapy to the patient.We present a 32 year old female patient, which is followed for 10 years with the diagnosis of sarcoidosis, initially with lung and lymph node involvement.Despite the good initial response to steroid therapy, the disease appears to be steroid-dependent and progressive, with multisystemic involvement. The steroids side-effects and the inefficiency of azathioprine as “steroid sparing agent” contribute to the difficulty in monitoring the progression of the disease.Given the unfavourable progression of sarcoidosis and the desire expressed by the patient to become pregnant, we present this case as a model of the challenges posed by this disease.
publishDate 2009
dc.date.none.fl_str_mv 2009-12-31
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 https://revista.spmi.pt/index.php/rpmi/article/view/1433
url https://revista.spmi.pt/index.php/rpmi/article/view/1433
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://revista.spmi.pt/index.php/rpmi/article/view/1433
https://revista.spmi.pt/index.php/rpmi/article/view/1433/984
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 Sociedade Portuguesa de Medicina Interna
publisher.none.fl_str_mv Sociedade Portuguesa de Medicina Interna
dc.source.none.fl_str_mv Internal Medicine; Vol. 16 No. 4 (2009): Outubro/ Dezembro; 247-252
Medicina Interna; Vol. 16 N.º 4 (2009): Outubro/ Dezembro; 247-252
2183-9980
0872-671X
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
repository.mail.fl_str_mv
_version_ 1799130749760176128