Primary Sjögren’s Syndrome – A theoretical revision

Bibliographic Details
Main Author: Coelho, Maria do Céu
Publication Date: 2002
Other Authors: Melo, Eduardo, Albuquerque, Ana, Saraiva, José Pedro, Pimentel, António
Format: Article
Language: por
Source: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Download full: https://revista.spmi.pt/index.php/rpmi/article/view/1861
Summary: Sjögren’s Syndrome is a slowly progressive, inflammatory autoimmune disease,affecting primarily the exocrine glands. Although ocular and oral exocrine glands are affected most commonly, giving rise to sicca symptoms (xerophthalmia, xerostomia), the clinical picture can be that of multisystem complaints, with symptoms/ signs that can be subtle and insidious, and therefore unrecognised.Some authors consider it “the great mimicker”. It can mimic or coexist with many other autoimmune organ-specific, haematological, or neurological disorders.These are some of the reasons why despite its relatively high prevalence, SS is often underdiagnosed, and some call it an “orphan disease”.The authors review clinical, immunological, histophatological aspects and therapeuticoptions of the disease.
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spelling Primary Sjögren’s Syndrome – A theoretical revisionSíndroma de Sjögren Primária – revisãoSindroma de SjögrenxerostomiaxeroftalmiaparotiditenefritepneumonitetiroidearteriteSjögren syndromexerostomiaxerophthalmiaparotitisnephritispneumonitisthyroiditisarthritisSjögren’s Syndrome is a slowly progressive, inflammatory autoimmune disease,affecting primarily the exocrine glands. Although ocular and oral exocrine glands are affected most commonly, giving rise to sicca symptoms (xerophthalmia, xerostomia), the clinical picture can be that of multisystem complaints, with symptoms/ signs that can be subtle and insidious, and therefore unrecognised.Some authors consider it “the great mimicker”. It can mimic or coexist with many other autoimmune organ-specific, haematological, or neurological disorders.These are some of the reasons why despite its relatively high prevalence, SS is often underdiagnosed, and some call it an “orphan disease”.The authors review clinical, immunological, histophatological aspects and therapeuticoptions of the disease.A síndroma de Sjögren (S.S.) é uma doença inflamatória auto-imune, lentamenteprogressiva que, predominantemente, afecta as glândulas exócrinas, clinicamentedominada pelos sintomas sicca (xerostomia e xeroftalmia), mas que pode, apresentar quadros clínicos diversos, com sintomas e sinais subtis, de desenvolvimento insidioso, e por isso, muitas vezes de reconhecimento e diagnóstico difícil.É considerada por alguns o “grande imitador”, pois pode mimetizar ou coexistir com outras doenças auto-imunes específicas de órgão, doenças hematológicas ou neurológicas.Atendendo a estas características, compreender-se-á que , sendo embora uma entidade comum, seja tão subdiagnosticada e alguns lhe chamem a “doença órfã ”.Os AA. fazem uma revisão teórica dos aspectos clínicos, histopatológicos,imunológicos e terapêuticos desta doença.Sociedade Portuguesa de Medicina Interna2002-09-30info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://revista.spmi.pt/index.php/rpmi/article/view/1861Internal Medicine; Vol. 9 No. 3 (2002): Julho/ SetembroMedicina Interna; Vol. 9 N.º 3 (2002): Julho/ Setembro2183-99800872-671Xreponame: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/1861https://revista.spmi.pt/index.php/rpmi/article/view/1861/1302Coelho, Maria do CéuMelo, EduardoAlbuquerque, AnaSaraiva, José PedroPimentel, Antónioinfo:eu-repo/semantics/openAccess2023-05-27T06:10:54Zoai:oai.revista.spmi.pt:article/1861Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:56:24.092470Repositório 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 Primary Sjögren’s Syndrome – A theoretical revision
Síndroma de Sjögren Primária – revisão
title Primary Sjögren’s Syndrome – A theoretical revision
spellingShingle Primary Sjögren’s Syndrome – A theoretical revision
Coelho, Maria do Céu
Sindroma de Sjögren
xerostomia
xeroftalmia
parotidite
nefrite
pneumonite
tiroide
arterite
Sjögren syndrome
xerostomia
xerophthalmia
parotitis
nephritis
pneumonitis
thyroiditis
arthritis
title_short Primary Sjögren’s Syndrome – A theoretical revision
title_full Primary Sjögren’s Syndrome – A theoretical revision
title_fullStr Primary Sjögren’s Syndrome – A theoretical revision
title_full_unstemmed Primary Sjögren’s Syndrome – A theoretical revision
title_sort Primary Sjögren’s Syndrome – A theoretical revision
author Coelho, Maria do Céu
author_facet Coelho, Maria do Céu
Melo, Eduardo
Albuquerque, Ana
Saraiva, José Pedro
Pimentel, António
author_role author
author2 Melo, Eduardo
Albuquerque, Ana
Saraiva, José Pedro
Pimentel, António
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Coelho, Maria do Céu
Melo, Eduardo
Albuquerque, Ana
Saraiva, José Pedro
Pimentel, António
dc.subject.por.fl_str_mv Sindroma de Sjögren
xerostomia
xeroftalmia
parotidite
nefrite
pneumonite
tiroide
arterite
Sjögren syndrome
xerostomia
xerophthalmia
parotitis
nephritis
pneumonitis
thyroiditis
arthritis
topic Sindroma de Sjögren
xerostomia
xeroftalmia
parotidite
nefrite
pneumonite
tiroide
arterite
Sjögren syndrome
xerostomia
xerophthalmia
parotitis
nephritis
pneumonitis
thyroiditis
arthritis
description Sjögren’s Syndrome is a slowly progressive, inflammatory autoimmune disease,affecting primarily the exocrine glands. Although ocular and oral exocrine glands are affected most commonly, giving rise to sicca symptoms (xerophthalmia, xerostomia), the clinical picture can be that of multisystem complaints, with symptoms/ signs that can be subtle and insidious, and therefore unrecognised.Some authors consider it “the great mimicker”. It can mimic or coexist with many other autoimmune organ-specific, haematological, or neurological disorders.These are some of the reasons why despite its relatively high prevalence, SS is often underdiagnosed, and some call it an “orphan disease”.The authors review clinical, immunological, histophatological aspects and therapeuticoptions of the disease.
publishDate 2002
dc.date.none.fl_str_mv 2002-09-30
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/1861
url https://revista.spmi.pt/index.php/rpmi/article/view/1861
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://revista.spmi.pt/index.php/rpmi/article/view/1861
https://revista.spmi.pt/index.php/rpmi/article/view/1861/1302
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. 9 No. 3 (2002): Julho/ Setembro
Medicina Interna; Vol. 9 N.º 3 (2002): Julho/ Setembro
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
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