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Information

 Bone and Soft-Tissue Disorders

= UNICAMERAL / SIMPLE BONE CYST

Frequency: up to 5% of primary bone lesions

Etiology: ? trauma (synovial entrapment at capsular reflection), ? vascular anomaly (blockage of interstitial drainage)

Histo: cyst filled with clear yellowish fluid often under pressure, wall lined with fibrous tissue + hemosiderin, giant cells may be present

Age: 3–19 years (80%); occurs during active phase of bone growth; M÷F = 3÷1

Location: proximal femur + proximal humerus (60–75%); fibula; at base of calcaneal neck (4%, >12 years of age); talus; rare in ribs, ilium, small bones of hand + feet; NOT in spine / calvarium; solitary lesion

Site: intramedullary centric metaphyseal, adjacent to epiphyseal cartilage (during active phase) / migrating into diaphysis with growth (during latent phase), does not cross epiphyseal plate

Prognosis: mostly spontaneous regression

Cx: pathologic fracture (65%)

DDx:

  1. Enchondroma (calcific stipplings)
  2. Fibrous dysplasia (more irregular lucency)
  3. Eosinophilic granuloma
  4. Chondroblastoma (epiphyseal)
  5. Chondromyxoid fibroma (more eccentric + expansile)
  6. Giant cell tumor
  7. Aneurysmal bone cyst (eccentric)
  8. Hemorrhagic cyst
  9. Brown tumor