Definition
chronic systemic inflammatory disorder affected synovium bone, cartilage, ligaments with extra-articular manifestationsRA is a chronic disease that leads to joint damage within the first 2 years, causes marked functional limitation and a 30% loss of work within the first 5 years, and shortens life by 5 to 7 years.
Epidemiology
RA occurs throughout the world and in all ethnic groups. The prevalence is lowest in black Africans and Chinese, and highest in the Pima Indians of Arizona. In Caucasians it is around 1.0-1.5% with a female:male ratio of 3:1. Before the age of 45, the female:male ratio is 6:1. Prevalence increases with age, with 5% of women and 2% of men over 55 years being affected.Etiology
Genetic factors. Family studies have demonstrated an increased risk for disease in siblings of persons affected with RA. Concordance in monozygotic has been found to be 12% to 15% and 4% in dizygotic twins.Enviromental
viruses (e.g., parvovirus B19, Epstein-Barr virus), Mycoplasma, and other bacteria (e.g., streptococci). Urbanization has a major impact on incidence & severity of R.A. cigarete smokingCellular immunity
Tissue PhaseHistopathology
The synovium of RA assumes the appearance of a reactive lymph node because of the extensive infiltration by plasma cells, macrophages, and lymphocytes in the form of large lymphoid follicles.
One characteristic feature of RA is the invasion of and damage to cartilage, bone, and tendons by an infiltrating inflammatory synovial tissue mass called the pannus
Clinical Characteristics of Rheumatoid Arthritis
Diagnosis of RA is made with four or more of the followingMorning stiffness (> 1 hour Arthritis of three or more joint areas Arthritis of hand joints Symmetrical arthritis Rheumatoid nodules Rheumatoid factor seropositive (rheumatoid factor positive ) Radiological changes Duration of 6 weeks or more
Articular Morning stiffness, "gelling"Symmetrical joint swellingPredilection for wrists, proximal interphalangeal, metacarpophalangeal, and metatarsophalangeal jointsErosions of bone and cartilageJoint subluxation and ulnar deviationInflammatory joint fluidCarpal tunnel syndromeBaker's cyst
Joints Affected : Typically involves elbows, wrists, MCP, and PIP joints 1st & 2nd cervical vertebrae frequently involved Unaffected joints : Thoracolumbar spine, DIPs & SI joints
Rheumatoid Arthritis: PIP Swelling
Swelling is confined to the area of the joint capsule Synovial thickening feels like a firm sponge*
Rheumatoid HAND
An across-the-room diagnosis Prominent ulnar deviation in the right hand MCP and PIP swelling in both hands MCP sublaxation Synovitis of left wrist
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hyperextension of the DIP joint of the finger (boutonniere deformity, occurs as a consequence of synovitis with stretching of, or rupture of, the PIP joint through the central extensor tendon with concomitant volar displacement of the lateral bands.
Hyperextension at the PIP joint with flexion of the DIP joint (swan-neck deformity, may be initiated by disruption of the extensor tendon at the DIP joint with secondary shortening of the central extensor tendon .
Rheumatoid arthritis: carpal tunnel syndrome, hand
*Rheumatoid arthritis: subluxation and muscle artrophy, hands
*Rheumatoid arthritis: ruptured right popliteal cyst
*EXTRA-ARTICULAR MANIFESTATIONS OF RHEUMATOID DISEASE
Haematological
Anaemia Thrombocytosis Eosinophilia
Lymphatic
Splenomegaly Felty's syndrome Nodules Sinuses FistulaeOcular
Eapiscleritis Scleritis Scleromalaciaa Keratoconjunctivitis siccaVasculitis
Digital arteritis Ulcers Pyoderma gangrenosum Mononeuritis multiplex Visceral arteritisCardiac
Pericarditis Myocarditis Endocarditis Conduction defects Coronary vasculitis Granulomatous aortitisPulmonary
Nodules Pleural effusions Fibrosing alveolitis Bronchiolitis Caplan's syndromeNeurological
Cervical cord compression Compression neuropathies Peripheral neuropathy Mononeuritis multiplexCutaneous features
Subcutaneous rheumatoid nodules occur almost exclusively in seropositive patients, usually at sites of pressure or friction such as the extensor surfaces of the forearm, sacrum, Achilles tendon and toesCardiovascular features
Asymptomatic pericarditis occurs in approximately 30% of patients with seropositive RA, with pericardial effusions and constrictive pericarditis being rare complications. Occasionally, granulomatous lesions result in heart block, cardiomyopathy, coronary artery occlusion or aortic regurgitation..Rheumatoid arthritis: subcutaneous nodule, olecranon
*Rheumatoid arthritis: episcleritis
*Rheumatoid arthritis: scleromalacia
*Rheumatoid arthritis: scleromalacia perforans
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Rheumatoid arthritis: scleromalacia perforans, herniation of the dark pigmented uveal tissue
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Rheumatoid arthritis: vasculitis with small infarcts, fingers
*Rheumatoid arthritis: vasculitis and gangrene, fingers
*Rheumatoid arthritis: pulmonary nodules
*Laboratory Tests
Raised inflammatory markers . Reasonable correlation with clinical activityMild anemia & thrombocytosisS. Rheumatoid factor (Agglutination method). Positive in near 70-80% cases (western countries). Not specificAnti-CCP (citrulline – containing proteins) antibodies. Similar sensitivity to RF but more specific (up to 95%) *Examination of joint fluid
the most helpful laboratory procedure. The fluid is inflammatory, with more than 10,000 white blood cells and a predominance of polymorphonuclear leukocytes, typically 80% or more. Rheumatoid factor, an IgM antibody directed to IgG, is found in 80 to 90% of patients with RA.... XR-Findings
Peri articular osteopenia Marginal erosions (at least months of persistent activity) Joint space narrowing (cartilage loss) Ankylosis (wrists) Deformities
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A. Soft-tissue swelling, no erosions B. Thinning of the cortex on the radial side and minimal joint space narrowing C. Marginal erosion at the radial side of the metacarpal head with joint space narrowing
Joint damage progression in R.A. hand
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Prognosis
The following factors at presentation are associated with a poor prognosis: higher baseline disability female gender involvement of MTP joints positive rheumatoid factor disease duration of over 3 months.*