hydroxyapatite deposition disease; calcium hydroxyapatite deposition disease; basic calcium phosphate deposition disease
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Etiology
- often occurs in the setting of trauma
Epidemiology
- mostly occurs in women
Pathology
- deposition of calcium hydroxyapatite in synovial joints & tendon sheaths
Clinical manifestations
- acute inflammation
- calcific tendonitis
- osteoarthritis
- periarthritis/arthritis dialysis syndrome
- rupture of calcinotic deposits in scleroderma
- chronic inflammation
- active motion is limited
- passive motion may be preserved
- may be asymptomatic
Laboratory
- synovial fluid
- individual crystals cannot be seen on routine polarization microscopy
- small, round bodies 0.5-100 um seen as lumps of crystals
- positive identification requires electron microscopy or elemental analysis
- Alizarin red staining for Ca+2 plus exclusion of CPPD provides presumptive diagnosis
- non-inflammatory: case[2] with 8300 leukocytes/uL
Radiology
- X-ray may show articular & periarticular dystrophic calcification