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Pathology – Benign Bone Tumors
I. Osteochondroma
  • Definition: Benign bone-forming tumour.
  • Location: Solitary exophytic nodule arising from the metaphysis of long bones near the epiphyseal growth plate.
  • Population: Common in children.
  • Histology:
    • Outer fibrous perichondrium.
    • Cartilage cap.
    • Underlying bony stalk.
  • Key takeaway: Think "bone spur" growing outwards from the growth plate of a long bone in a child.
II. Chondroma
  • Definition: Benign cartilage-forming tumour.
  • Location: Two main types:
    • Enchondromas: Medulla of bones (hands and feet are common).
    • Periosteal chondromas: Surface of bone (proximal humerus is characteristic).
  • Presentation: Often discovered incidentally (no symptoms).
  • Histology: Chondrocytes within an abundant cartilaginous matrix.
  • Key takeaway: Cartilage-based tumour, location distinguishes the subtypes.
III. Osteoid Osteoma
  • Definition: Benign bone-forming tumour.
  • Location: Long bones of children/young adults (proximal femur is common).
  • Presentation: Characteristic nocturnal pain.
  • Radiographic Appearance: Small lucent nidus (<1cm) on plain radiographs.< />pan>
  • Histology: Well-circumscribed, hypervascular area of bony trabeculae surrounded by reactive bone.
  • Key takeaway: Small, painful lesion easily visualized on X-ray; pain is a key clinical feature.
IV. Giant Cell Tumour of Bone (GCTB)
  • Definition: Benign, but locally aggressive neoplasm.
  • Location: Ends of long bones.
  • Population: Young adults (20-45 years).
  • Presentation: Pain and swelling at the tumour site.
  • Histology: Sheets of neoplastic ovoid mononuclear cells with interspersed large osteoclast-like giant cells.
  • Prognosis: ~25% local recurrence rate after excision. Distant metastasis is rare.
  • Key takeaway: Although benign, its local aggressiveness and potential for recurrence are significant.
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