Primary Sjögren’s Syndrome – A theoretical revision

Authors

  • Maria do Céu Coelho Médica do Internato Complementar de Medicina Interna, Hospital de São Teotónio, Viseu
  • Eduardo Melo Assistente de Medicina Interna (UCIP), Hospital de São Teotónio, Viseu
  • Ana Albuquerque Assistente de Medicina Interna (UCIP), Hospital de São Teotónio, Viseu
  • José Pedro Saraiva Assistente Graduado de Anestesiologia (UCIP), Hospital São Teotónio, Viseu
  • António Pimentel Director de Serviço da Unidade de Cuidados Intensivos Polivalente (UCIP), Hospital de São Teotónio, Viseu

Keywords:

Sjögren syndrome, xerostomia, xerophthalmia, parotitis, nephritis, pneumonitis, thyroiditis, arthritis

Abstract

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 therapeutic
options of the disease.

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Additional Files

Published

2002-09-30

How to Cite

1.
Coelho M do C, Melo E, Albuquerque A, Saraiva JP, Pimentel A. Primary Sjögren’s Syndrome – A theoretical revision. RPMI [Internet]. 2002 Sep. 30 [cited 2024 Oct. 17];9(3). Available from: https://revista.spmi.pt/index.php/rpmi/article/view/1861

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