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Published byShana Richard Modified over 9 years ago
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DR.A.Tahamoli Rudsari
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Rheumatoid arthritis (RA) is a chronic multisystem disease of unknown cause. Although there are a variety of systemic manifestations, the characteristic feature of established RA is chronic inflammatory symmetric polyarthritis.
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The prevalence of RA is 0.5 – 1% of the adult population. Women are affected approximately three times more often than men. 25 – 50 y
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RA is found at approximately 2 -10 times the expected rate in first-degree relatives of RA patients. 10 – 25 % The class II major histocompatibility complex allele are known to be major genetic risk factors for RA. HLA-DRB1 PTPN22
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Smoking EBV
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RA affects the synovial tissue and underlying cartilage and bone. The pathologic hallmarks of RA are synovial inflammation and proliferation, focal bone erosions, and thinning of articular cartilage.
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Pathogenesis
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Articular manifestation Exteraarticular manifestation
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Chronic inflammatory symmetric polyarthritis
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extraarticular features
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RF Anti CCP CBC, ESR, CRP, BUN, Cr, AST, AIT, … Synovial fluid analysis
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Early in the disease, radiographic evaluations of the affected joints are usually not helpful in establishing a diagnosis. Plain radiography
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NSAIDs Glucocorticoids DMARDs HCQ MTX SSZ LEF
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Biological DMARDs Anti – TNF agents Rituximab Anakinra Abatacept Tocilizumab
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Sjögren's syndrome is a chronic, slowly progressive autoimmune disease characterized by lymphocytic infiltration of the exocrine glands resulting in xerostomia and dry eyes.
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Approximately one-third of patients present with systemic manifestations. Primary Sjögren's syndrome Secondary Sjögren's syndrome
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The prevalence of primary Sjögren's syndrome is approximately 0.5–1.0%, while 30% of patients with autoimmune rheumatic diseases suffer from secondary Sjögren's syndrome.
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RA SLE SSC MCTD PBC Vasculitis CAH
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Middle-aged women are primarily affected. Female/Male : 9/1
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Exocrine gland features Extraglandular disease features 8–10 years may elapse from the initial symptoms to full-blown development of the disease.
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The principal oral symptom of Sjögren's syndrome is dryness (xerostomia). Physical examination shows a dry, erythematous, sticky oral mucosa. Enlargement of the parotid or other major salivary glands occurs in two-thirds of patients with primary Sjögren's syndrome but is uncommon in those with the secondary syndrome.`
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Patients usually complain of a sandy or gritty feeling under the eyelids. Other symptoms include burning, accumulation of thick strands at the inner canthi, decreased tearing, redness, itching, eye fatigue, and increased photosensitivity. keratoconjunctivitis sicca
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Extraglandular (systemic) manifestations are seen in one-third of patients with Sjögren's syndrome, while they are very rare in patients with Sjögren's syndrome associated with rheumatoid arthritis.
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Anti Ro/SS-A Anti La/SS-B
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