CONFIRMING DIAGNOSIS X-rays confirm joint involvement and show:
❑ erosion of terminal phalangeal tufts
❑ “whittling” of the distal end of the terminal phalanges
❑ “pencil-in-cup” deformity of the distal interphalangeal joints
❑ relative absence of osteoporosis
❑ sacroiliitis
❑ atypical spondylitis with syndesmophyte formation. Hyperostosis and paravertebral ossification result, which may lead to vertebral fusion.
Blood studies indicate negative rheumatoid factor and elevated erythrocyte sedimentation rate and uric acid levels.
» READ BOOK EXCERPT ONLINE »
Source: Professional Guide to Diseases (Eighth Edition), 2005
Rheumatoid arthritis:
Diagnosis
(Professional Guide to Diseases (Eighth Edition))
Typical clinical features suggest this disorder, but a definitive diagnosis is based on laboratory and other test results:
❑ X-rays — in early stages, show bone demineralization and soft-tissue swelling; later, loss of cartilage and narrowing of joint spaces; finally, cartilage and bone destruction and erosion, subluxations, and deformities
❑ rheumatoid factor test — positive in 75% to 80% of patients as indicated by a titer of 1:160 or higher
❑ synovial fluid analysis — reveals increased volume and turbidity but decreased viscosity and complement (C3 and C4) levels; white blood cell count usually exceeds 10,000/µl
❑ erythrocyte sedimentation rate — elevated in 85% to 90% of patients (may be useful to monitor response to therapy because elevation commonly parallels disease activity)
❑ complete blood count — usually reveals moderate anemia and slight leukocytosis.
A C-reactive protein test can help monitor response to therapy.
» READ BOOK EXCERPT ONLINE »
Source: Professional Guide to Diseases (Eighth Edition), 2005
Osteoarthritis:
Diagnosis
(Professional Guide to Diseases (Eighth Edition))
A thorough physical examination confirms typical symptoms, and absence of systemic symptoms rules out an inflammatory joint disorder. X-rays of the affected joint help confirm diagnosis of osteoarthritis but may be normal in the early stages. X-rays may require many views and typically show:
❑ narrowing of joint space or margin
❑ cystlike bony deposits in joint space and margins and sclerosis of the subchondral space
❑ joint deformity due to degeneration or articular damage
❑ bony growths at weight-bearing areas
❑ fusion of joints. (See Digital joint deformities, page 591.)
» READ BOOK EXCERPT ONLINE »
Source: Professional Guide to Diseases (Eighth Edition), 2005
Juvenile rheumatoid arthritis:
Diagnosis
(Professional Guide to Diseases (Eighth Edition))
Persistent joint pain and the rash and fever clearly point to JRA. Laboratory tests are useful for ruling out other inflammatory or even malignant diseases that can mimic JRA. Disease activity and response to therapy can also be monitored through laboratory results.
❑ Complete blood count shows decreased hemoglobin levels, neutrophilia, and thrombocytosis.
❑ Erythrocyte sedimentation rate and C-reactive protein, haptoglobin, immunoglobulin, and C3 complement levels may be elevated.
❑ ANA test may be positive in patients who have pauciarticular JRA with chronic iridocyclitis.
❑ RF is present in 15% of JRA cases, compared with 85% of rheumatoid arthritis cases.
❑ Positive HLA-B27 antigens may forecast later development of ankylosing spondylitis.
❑ X-rays in early stages reveal changes, including soft-tissue swelling, effusion, and periostitis in affected joints. Later, osteoporosis and accelerated bone growth may appear, followed by subchondral erosions, joint space narrowing, bone destruction, and fusion.
» READ BOOK EXCERPT ONLINE »
Source: Professional Guide to Diseases (Eighth Edition), 2005
Psoriatic arthritis:
Diagnosis
(Handbook of Diseases)
Inflammatory arthritis in a patient with psoriatic skin lesions suggests psoriatic arthritis. X-rays confirm joint involvement and show:
❑ marginal erosion at interphalangeal joints with areas of thin, “fluffy” new bone formation
❑ “whittling” of the distal end of the terminal phalanges
❑ “pencil-in-cup” deformity of the distal interphalangeal joints
❑ relative absence of osteoporosis
❑ sacroiliitis
❑ atypical spondylitis with syndesmophyte formation, resulting in hyperostosis and paravertebral ossification, which may lead to vertebral fusion.
Blood studies indicate negative rheumatoid factor and elevated erythrocyte sedimentation rate and uric acid levels.
» READ BOOK EXCERPT ONLINE »
Source: Handbook of Diseases, 2003
Rheumatoid arthritis:
Diagnosis
(Handbook of Diseases)
Typical signs and symptoms suggest RA, with a firm diagnosis supported by laboratory and other test results:
❑ X-raysin early stages show bone demineralization and soft-tissue swelling; later, loss of cartilage and narrowing of joint spaces; and finally, cartilage and bone destruction and erosion, subluxations, and deformities.
❑ RF is positive in 75% to 80% of patients, as indicated by a titer of 1:160 or higher.
❑ Synovial fluid analysisshows increased volume and turbidity but decreased viscosity and elevated white blood cell counts (often greater than 10,000/µl).
❑ Serum protein electrophoresis may show elevated serum globulin levels.
❑ Erythrocyte sedimentation rate and C-reactive protein are elevated in 85% to 90% of patients (may be useful to monitor response to therapy because elevation typically parallels disease activity).
❑ Complete blood count usually shows moderate anemia, slight leukocytosis, and thrombocytosis.
» READ BOOK EXCERPT ONLINE »
Source: Handbook of Diseases, 2003
Osteoarthritis:
Diagnosis
(Handbook of Diseases)
A thorough physical examination confirms typical symptoms, and the absence of systemic symptoms rules out an inflammatory joint disorder. X-rays of the affected joint help confirm diagnosis of osteoarthritis but may be normal in the early stages. X-rays may require many views and typically show:
❑ narrowing of joint space or margin
❑ cystlike bony deposits in joint space and margins
❑ sclerosis of the subchondral space
❑ joint deformity due to degeneration or articular damage
❑ bony growths at weight-bearing areas
❑ fusion of joints.
No laboratory test is specific for osteoarthritis.
» READ BOOK EXCERPT ONLINE »
Source: Handbook of Diseases, 2003
Juvenile rheumatoid arthritis:
Diagnosis
(Handbook of Diseases)
Persistent joint pain, rash, and fever clearly point to JRA. Laboratory tests are useful for ruling out other inflammatory or even malignant diseases that can mimic JRA and for monitoring disease activity and response to therapy.
❑ Complete blood count shows decreased hemoglobin levels, neutrophilia, and thrombocytosis.
❑ Erythrocyte sedimentation rate, complement (C)-reactive protein, haptoglobin, immunoglobulin, and C3 levels may be elevated.
❑ Test results may be positive for ANAs in patients who have pauciarticular JRA with chronic iridocyclitis.
❑ RF is present in 15% of patients with JRA, as compared with 85% of patients with RA.
❑ Positive HLA-B27 test may forecast later development of ankylosing spondylitis.
❑ Early X-ray changes include soft-tissue swelling, effusion, and periostitis in affected joints. Later, osteoporosis and accelerated bone growth may appear, followed by subchondral erosions, joint space narrowing, bone destruction, and fusion.
» READ BOOK EXCERPT ONLINE »
Source: Handbook of Diseases, 2003
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