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For further information, see CMDT Part 22-05: Rheumatoid Arthritis
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Essentials of Diagnosis
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Usually insidious onset with morning stiffness and joint pain
Symmetric polyarthritis with predilection for small joints of the hands and feet; deformities common with progressive disease
Radiographic findings
Rheumatoid factor and antibodies to cyclic citrullinated peptides (anti-CCP) are present in 70–80% (Table 22–6)
Extra-articular manifestations: subcutaneous nodules, interstitial lung disease, pleural effusion, pericarditis, splenomegaly, scleritis, and vasculitis.
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General Considerations
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Chronic systemic inflammatory disease whose major manifestation is synovitis of multiple joints
Cause is unknown
Multiple genes contribute to susceptibility; best characterized genetic risk factor is inheritance of HLA-DRB1 alleles encoding a distinctive five-amino-acid sequence known as the "shared epitope"
The pathologic findings in the joint include
Chronic synovitis with formation of a pannus, which erodes cartilage, bone, ligaments, and tendons
Effusion and other manifestations of inflammation are common
In the late stage, organization may result in fibrous ankylosis; true bony ankylosis is rare
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Prevalence is 1%
More common in women than in men (female:male ratio of 3:1)
Can begin at any age, but the peak onset is in the fourth or fifth decade for women and the sixth to eighth decades for men
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Joint symptoms
Onset of articular signs of inflammation is usually insidious, with prodromal symptoms of vague periarticular pain or stiffness
Symmetric swelling of multiple joints with tenderness and pain
Monoarticular disease is occasionally seen initially
Stiffness
Distribution of affected joints
Proximal interphalangeal (PIP) joints of the fingers, metacarpophalangeal (MCP) joints, wrists, knees, ankles, and metatarsophalangeal (MTP) ...