2012
DOI: 10.1016/j.jaut.2011.12.006
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Classification criteria for Sjogren’s syndrome: A critical review

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Cited by 114 publications
(82 citation statements)
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References 29 publications
(43 reference statements)
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“…Sjögren's syndrome is an autoimmune disorder of the connective tissue leading to the reduction of secretory functions of salivary and lacrimal glands [1,2]. The disease affects nearly 1.7 million people in the European Union and around 1 million people in the United States (~90% of them are middle-aged women) [3].…”
Section: Introductionmentioning
confidence: 99%
“…Sjögren's syndrome is an autoimmune disorder of the connective tissue leading to the reduction of secretory functions of salivary and lacrimal glands [1,2]. The disease affects nearly 1.7 million people in the European Union and around 1 million people in the United States (~90% of them are middle-aged women) [3].…”
Section: Introductionmentioning
confidence: 99%
“…Sjogren's syndrome has a wide clinical and immunologic spectrum and may progress from an exocrinopathy to a systemic disease with a variety of extraglandular manifestations and/ or associated autoimmune diseases. The difficulty in diagnosis is reflected on continuous review attempts of the 7 classification criteria that have been created in the past 25 years [13]. However, histological analysis of labial salivary gland biopsy (LSGB) is mostly a method of great importance according to the American-European Group Consensus (AEGC) criteria [14].…”
Section: Case Reportmentioning
confidence: 99%
“…Sjögren's syndrome (SS) is a chronic, systemic autoimmune disorder which affects typically the exocrine glands associated with/ without every other systemic autoimmune rheumatic disorder [1,2]. The ocular and oral dryness can be caused by a typical focal lymphocytic infiltration of the lacrimal and salivary glands [1].…”
Section: Introductionmentioning
confidence: 99%
“…The ocular and oral dryness can be caused by a typical focal lymphocytic infiltration of the lacrimal and salivary glands [1]. Its wide clinical spectrum includes not only benign local exocrinopathy (dry eyes, dry mouth) but also systemic disorder that affects parenchymal organs (liver, kidneys, lung), lesions owing to immune complex hyperproduction and/or vasculitic involvement (glomerulonephritis, peripheral neuropathy, purpura), and lymphocytic malignancies which is known to occur in 5% of SS patients [3].…”
Section: Introductionmentioning
confidence: 99%
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