joint disease; articular disease; arthropathy
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Introduction
Joint disease characterized by 3 parameters:
- acute vs chronic
- inflammatory vs non-inflammatory
- monoarticular vs oligoarticular (2-4 joints) vs polyarticular
Etiology
- acute inflammation
- chronic inflammation
- chronic without inflammation
Clinical manifestations
- inflammatory:
- erythema, warmth, edema
- morning stiffness > 60 minutes
- constitutional symptoms: fever, fatigue, malaise
- non-inflammatory
- no erythema, minimal warmth, no edema, bony enlargement, joint effusion
- morning stiffness < 30 minutes
- constitutional symptoms: usually none
Laboratory
- synovial fluid
- appearance
- normal & non-inflammatory: clear/yellow/transparent
- inflammatory & crystalline arthropathy: yellow/white/translucent/opaque
- infectious: yellow/white/opaque
- hemorrhagic: red/opaque
- leukocyte count
- < 200/uL is normal
- 200-2000/uL (non-inflammatory), predominantly monocytes
- 2000-20,000/uL or higher (inflammatory)
- predominantly neutrophils (acute), monocytes (chronic)
- 10,000-50,000/uL (crystalline arthropathy)
- > 50,000/uL may be lower (infectious arthropathy)
- gram stain & culture for suspected infectious etiology
- appearance
- erythrocyte sedimentation rate is elevated with inflammatory arthritis
- C-reactive protein in serum is elevated with inflammatory arthritis
- complete blood count (CBC): anemia of chronic inflammation
- serology: see autoantibodies in rheumatologic disease
More general terms
More specific terms
- 2nd & 3rd metacarpophalangeal (MCP) arthropathy
- abscess of bursa
- acromioclavicular joint degeneration; acromioclavicular arthritis
- ankylosis
- arthritis
- arthrogryposis
- bunion
- cervicocranial syndrome
- cheiroarthropathy
- cheiropathy
- claw toe
- Clutton's joints
- costochondritis (Tietze syndrome)
- degenerative joint disease (DJD)
- enthesopathy (enthesitis)
- femoroacetabular impingement
- hallux limitus/rigidus
- hallux valgus
- hallux varus
- hammertoe; hallux malleus; digiti flexus
- hemarthrosis
- joint deformity
- joint dislocation
- joint instability
- joint mouse
- mallet finger
- osteoarthropathy
- pachydermodactyly
- pigmented villonodular synovitis (PVNS)
- Plica syndrome
- polymyalgia arthralgia syndrome (PMAS)
- rotator cuff disease
- Stickler syndrome or hereditary progressive arthroophthalmopathy
- synostosis
- synovial chondromatosis; Reichel's syndrome; Reichel-Jones-Henderson syndrome
- synovial osteochondromatosis (SOC)
- temporomandibular joint (TMJ) syndrome
Additional terms
References
- ↑ Waits JB. Rational use of laboratory testing in the initial evaluation of soft tissue and joint complaints. Prim Care. 2010 Dec;37(4):673-89, PMID: https://www.ncbi.nlm.nih.gov/pubmed/21050950
- ↑ Medical Knowledge Self Assessment Program (MKSAP) 19 Board Basics. An Enhancement to MKSAP19. American College of Physicians, Philadelphia 2022