Benign bone tumors
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Differential Diagnosis[1]
| Name | Presentation | Radiograph Findings/Location | Clinical Importance |
| Chondroblastoma | Bone or joint pain in adolescent | Epiphysis of long bones, may cross growth plate | Growth disturbance, arthritis |
| Enchondroma | Soft tissue mass in hands or feet of adolescent; seen in Ollier Disease or Mafucci Syndrome | Metaphysis of long bones in hands or feet; oval lesion with sclerotic edges and central lucency | Malignant transformation to chondrosarcoma if multiple lesions present |
| Langerhans cell histiocytosis of bone | Painful swelling of skull in children, typically frontal bone, or long bones | Lytic, punched out lesion | Lesion of skull can be associated with diabetes insipidus or other CNS disease; pathological fracture of long bone |
| Osteoblastoma | Adolescent male with chronic pain in spine, most often seen in posterior column | Similar to osteoid osteoma but typically > 2cm | May appear like osteoid osteoma on plain film but DOES NOT respond to Aspirin/NSAIDs |
| Osteochondroma | Adolescent male with painless mass over distal femur | Osseous spur that arises from cortex pointing away from joint | Observation without treatment; small risk of transformation to chondrosarcoma |
| Osteoid Osteoma | Adolescent male with bone pain over femur; pain worse at night and unrelated to activity | Radiolucent nidus with sclerotic edges most often seen in proximal femur | Nidus produces prostaglandins, Aspirin/NSAIDs can relieve pain; most soft resolve |
See Also
References
- ↑ Czerniak, Bogdan. “Benign Osteoblastic Tumors.” Dorfman and Czerniak's bone tumors. Elsevier Health Sciences, 2015, pp. 144 – 199.
