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Manar Hajeer, MD, FRCPath University of Jordan, school of medicine Degeneration……..osteoarthritis Immune-mediated injury……rheumatoid arthritis. Metabolic derangements……gout and pseudogout. Infections…….infectious arthritis Neoplasms. Degenerative joint disease. Most common joint disorder. Part of aging. Physical disability over the age of 65. Degeneration of articular cartilage; any structural changes in the underlying bone are secondary. Friction free movement along with the synovial fluid. Spreads the load across the joint surface so underlying bones can absorb shock and weight. OA is not exclusively a wear-and-tear phenomenon, but mechanical stresses and aging figure prominently. Genetic factors also seem to contribute to osteoarthritis susceptibility. Insidiously with age, without initiating cause (primary osteoarthritis). In youger patients, predisposing conditions: previous traumatic injury, developmental deformity, or systemic disease such as diabetes, hemochromatosis, or marked obesity (secondary osteoarthritis) knees and hands are more commonly affected in women. Hips are more commonly affected in men. Earliest changes :increasing water content of the cartilage with decreasing elasticity. Vertical and horizontal fibrillation and cracking occur in the superficial layers of the cartilage Full-thickness portions of the cartilage are lost. Subchondral bone is exposed. Small fractures can dislodge pieces of cartilage and subchondral bone into the joint, forming loose bodies (joint mice). Mushroom-shaped osteophytes (bony outgrowths) develop at the margins of the articular surface. No fusion of bone. Insidious disease Predominantly 50s and 60s. Deep, aching pain exacerbated by use, relieved by rest. Morning stiffness, crepitus , and limited range of movement. Osteophyte impingement on spinal foramina can cause nerve root compression with radicular pain, muscle spasms, muscle atrophy, and neurologic deficits. Hips, knees, lower lumbar and cervical vertebrae, proximal and distal interphalangeal joints of the fingers, first carpometacarpal joints, and first tarsometatarsal joints of the feet are commonly involved Heberden nodes in the fingers: prominent osteophytes at the distal interphalangeal joints, are characteristic in women. No predicted way to prevent progression of primary osteoarthritis. Can stabilize for years but is generally slowly progressive. With time, significant joint deformity can occur, but unlike rheumatoid arthritis , fusion does not take place Chronic autoimmune inflammatory disorder. Primarily affecting small joints of the hands and feet. Joints producing a proliferative synovitis that often progresses to destruction of the articular cartilage. 3:1 to 5:1 , female to male ratio. Peak incidence: second to fourth decades of life. No age is immune. Symmetric arthritis. Small joints of the hands and feet, ankles, knees, wrists, elbows, and shoulders. Typically, the proximal interphalangeal and metacarpophalangeal joints are affected. Distal interphalangeal joints are spared. Axial involvement limited to upper cervical spine; similarly. Hip joint involvement is extremely uncommon. Chronic synovitis, Periarticular soft tissue edema usually develops (fusiform swelling of the proximal interphalangeal joints). With progression, the articular cartilage is eroded and, in time, virtually destroyed. Subarticular bone may be attacked and eroded. XRAY hallmarks: joint effusions , juxta-articular osteopenia, narrowing of the joint space and loss of articular cartilage. Destruction of tendons, ligaments, and joint capsules>>>joint deformities: Radial deviation of the wrist. Ulnar deviation of the fingers. Flexion-hyperextension abnormalities of the fingers (swan-neck deformity, boutonnière deformity). Rheumatoid subcutaneous nodules: 25% of patients, along extensor surface of the forearm or areas subjected to mechanical pressure. Rarely in the lungs, spleen, heart, aorta. Rheumatoid nodules are firm, non-tender, oval or rounded masses as large as 2 cm in diameter. 80% of patients have serum autoantibodies, called rheumatoid factor (RF). 1. 2. 3. 4. 5. 6. 7. Severe joint pain and morning stiffness. Arthritis in 3 or more joint areas. Arthritis of small hand joints. Symmetric arthritis. Rheumatoid nodules. Serum rheumatoid factor. Typical radiographic changes At least four features are needed for the diagnosis. Constitutional symptoms: weakness, malaise, and low-grade fever. Joints enlarged, motion limited, complete deformities may appear. Sterile, turbid synovial fluid. Microorganisms of any type can lodge in joints during : (1)hematogenous dissemination. (2)contiguous spread from osteomyelitis or a soft tissue abscess. Infectious arthritis is serious because it can cause rapid joint destruction and permanent deformities. Acute Suppurative Arthritis Bacterial in origin: Haemophilus influenzae predominates in children under age 2 years. S. aureus is the main causative agent in older children and adults. gonococcus is prevalent during late adolescence and young adulthood. Individuals with sickle cell disease are prone to infection with Salmonella at any age Sudden onset of pain, redness, and swelling of the joint with restricted range of motion. Fever, leukocytosis, and elevated ESR. In 90% of nongonococcal suppurative arthritis, the infection involves only a single joint-usually the kneefollowed in order by hip, shoulder, elbow, wrist, and sternoclavicular joints. Joint aspiration is typically purulent, and allows identification of the causal agent. Acquired diseases of bone (osteoporosis and osteomalacia). Osteomyelitis. Bone tumors. Acquired condition. Reduced bone mass, leading to bone fragility and susceptibility to fractures. Osteoporosis occurs when the dynamic balance between bone formation by osteoblasts and bone resorption by osteoclasts tilts in favor of resorption. Primary versus secondary forms. Primary osteoporosis: most common and may be associated with aging (senile osteoporosis) or the postmenopausal state in women. The drop in estrogen following menopause tends to exacerbate the loss of bone that occurs with aging, placing older women at high risk of osteoporosis relative to men. Bone mass peaks during young adulthood. The greater the peak bone mass, the greater the delay in onset of osteoporosis. The bone loss, averaging 0.5% per year, is a seemingly inevitable consequence of aging and is most prominent in the spine and femoral neck. Increase in the risk of fractures. Hallmark is a loss of bone. Osteoclastic activity is present but is not dramatically increased. Mineral content of the bone tissue is normal. In senile osteoporosis, cortical bone loss is prominent, predisposing to fractures in weight-bearing bones, such as the femoral neck. vitamin D deficiency. Impairment of mineralization and a resultant accumulation of unmineralized matrix. Contrasts with osteoporosis, in which the mineral content of the bone is normal and the total bone mass is decreased. Rickets :vitamin D defficiency in children, in which it interferes with the deposition of bone in the growth plates. Osteomalacia: the adult counterpart, bone formed during remodeling is undermineralized, resulting in predisposition to fractures. Osteomyelitis is defined as inflammation and infection of bone and marrow. Osteomyelitis can be secondary to systemic infection but more frequently occurs as a primary isolated focus of disease; it can be an acute process or a chronic debilitating illness. Any microorganism can cause osteomyelitis, the most common etiologic agents are pyogenic bacteria and Mycobacterium tuberculosis. Acute osteomyelitis Routes: (1) hematogenous dissemination (most common); (2) extension from an infection in adjacent joint or soft tissue; (3) traumatic implantation after compound fractures or orthopedic procedures. Staphylococcus aureus is the most frequent causative organism; Escherichia coli and group B streptococci are important causes in neonates, Salmonella is an common pathogen in persons with sickle cell disease. Osteomyelitis classically manifests as an acute systemic illness, with malaise, fever, leukocytosis, and throbbing pain over the affected region. Symptoms also can be subtle, with only unexplained fever, particularly in infants, or only localized pain in the adult. A combination of antibiotics and surgical drainage usually is curative, but up to a quarter of cases do not resolve and persist as chronic infections In infants epiphyseal infection can spread into the adjoining joint to produce suppurative arthritis, Pathologic fracture, Sepsis and endocarditis, Rarely development of squamous cell carcinoma if the infection creates a sinus tract, Rarely osteosarcoma.