Bone tumors and their mimics

Benign[1]

Name Presentation Radiograph Findings/Location Clinical Importance
ChondroblastomaBone or joint pain in adolescentEpiphysis of long bones, may cross growth plateGrowth disturbance, arthritis
EnchondromaSoft tissue mass in hands or feet of adolescent; seen in Ollier Disease or Mafucci SyndromeMetaphysis of long bones in hands or feet; oval lesion with sclerotic edges and central lucencyMalignant transformation to chondrosarcoma if multiple lesions present
Langerhans cell histiocytosis of bonePainful swelling of skull in children, typically frontal bone, or long bonesLytic, punched out lesionLesion of skull can be associated with diabetes insipidus or other CNS disease; pathological fracture of long bone
OsteoblastomaAdolescent male with chronic pain in spine, most often seen in posterior columnSimilar to osteoid osteoma but typically > 2cmMay appear like osteoid osteoma on plain film but DOES NOT respond to Aspirin/NSAIDs
OsteochondromaAdolescent male with painless mass over distal femurOsseous spur that arises from cortex pointing away from jointObservation without treatment; small risk of transformation to chondrosarcoma
Osteoid OsteomaAdolescent male with bone pain over femur; pain worse at night and unrelated to activityRadiolucent nidus with sclerotic edges most often seen in proximal femurNidus produces prostaglandins, Aspirin/NSAIDs can relieve pain; most soft resolve

Malignant[2]

Name Presentation Radiograph Findings Clinical Importance
AdamantinomaBone pain over anterior tibia in adolescent or young adultSoap bubble osteolytic appearance on plain radiographMetastasis to lungs; may need amputation
ChordomaConstant pain if in sacrum; neurological deficits if at base of skull, most commonly in cranial nerves to the eyePlain radiograph will show a destructive bone lesion often with an associated soft tissue massSlow growing but locally aggressive; metastasis is uncommon, local recurrence is much more likely
Fibrosarcoma and Undifferentiated pleomorphic sarcomaSimilar to osteosarcoma except malignant fibroblasts but less commonMost common in distal femur and proximal tibiaSimilar outcome to osteosarcoma
Primary bone lymphomaAdult > 40 years of age with bone pain or pathologic fractureBone destruction; soft tissue mass5 year survival is greater than 50% with radiation and chemotherapy

Differential Diagnosis

Bone tumors and their mimics

Malignant

Benign

  • Giant cell tumor
  • Chrondroblastoma
  • Enchondroma
  • Langerhans cell histiocytosis of bone
  • Osteoblastoma
  • Osteochondroma
  • Osteoid osteoma

Other

See Also

  • Benign bone tumors
  • Malignant bone tumors

References

  1. Czerniak, Bogdan. “Benign Osteoblastic Tumors.” Dorfman and Czerniak's bone tumors. Elsevier Health Sciences, 2015, pp. 144 – 199.
  2. Niederhuber, John E., et al. “Sarcomas.” Abeloff's Clinical Oncology E-Book. Elsevier Health Sciences, 2019, pp. 1604 – 1654.e8.
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