Bone tumors and their mimics
Benign[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 |
Malignant[2]
Name | Presentation | Radiograph Findings | Clinical Importance |
Adamantinoma | Bone pain over anterior tibia in adolescent or young adult | Soap bubble osteolytic appearance on plain radiograph | Metastasis to lungs; may need amputation |
Chordoma | Constant pain if in sacrum; neurological deficits if at base of skull, most commonly in cranial nerves to the eye | Plain radiograph will show a destructive bone lesion often with an associated soft tissue mass | Slow growing but locally aggressive; metastasis is uncommon, local recurrence is much more likely |
Fibrosarcoma and Undifferentiated pleomorphic sarcoma | Similar to osteosarcoma except malignant fibroblasts but less common | Most common in distal femur and proximal tibia | Similar outcome to osteosarcoma |
Primary bone lymphoma | Adult > 40 years of age with bone pain or pathologic fracture | Bone destruction; soft tissue mass | 5 year survival is greater than 50% with radiation and chemotherapy |
Differential Diagnosis
Malignant
- Multiple myeloma
- Chondrosarcoma
- Paget disease
- Osteosarcoma
- Adamantinoma
- Chordoma
- Primary bone lymphoma
- Fibrosarcoma
- Myosarcoma
Benign
- Giant cell tumor
- Chrondroblastoma
- Enchondroma
- Langerhans cell histiocytosis of bone
- Osteoblastoma
- Osteochondroma
- Osteoid osteoma
See Also
- Benign bone tumors
- Malignant bone tumors
References
- Czerniak, Bogdan. “Benign Osteoblastic Tumors.” Dorfman and Czerniak's bone tumors. Elsevier Health Sciences, 2015, pp. 144 – 199.
- Niederhuber, John E., et al. “Sarcomas.” Abeloff's Clinical Oncology E-Book. Elsevier Health Sciences, 2019, pp. 1604 – 1654.e8.
This article is issued from
Wikem.
The text is licensed under Creative
Commons - Attribution - Sharealike.
Additional terms may apply for the media files.