Classification – Predominant Tissue

Tissue of OriginBenignMalignant
Bone formingOsteoma
Osteoid Osteoma
Osteoblastoma
Osteosarcoma
Cartilage formingChondroma
Osteochondroma
Chondroblastoma
Chondrosarcoma
Fibrous tissueFibromaFibrosarcoma
Giant-cell tumorBenign OsteoclastomaMalignant Osteoclastoma
Marrow tumorsEwing’s Sarcoma
Myeloma
VascularHaemangiomaHaemangiosarcoma
Other connective tissueFibrous histocytoma
Lipoma
Malignant fibrous histocytoma
Liposarcoma
Other tumorsNeurofibromaAdamantina

Clinical Presentation

History

Duration

  • Prolonged history:
    • In most benign lesions
    • Some malignant:
      • Slow growing (chondrosarcoma) / in pelvis (expandable)

Age Distribution

  • Childhood and adolescence
    • Most benign, and some malignant (e.g. Ewing’s sarcoma)
  • 4th – 5th decade:
    • Chondrosarcoma
  • Sixth decade:
    • Myeloma (the commonest primary malignant bone tumor)
  • Over 50 yrs.:
    • Metastatic lesions are the commonest

Symptoms

  • Pain:
    • In both malignant and benign (usually more in malignant)
    • May be caused by:
      • Rapid expansion – stretching of tissues
      • Central hemorrhage or degeneration
      • Insipient pathological fracture
      • Tense encapsulation in bone (e.g. osteoid osteoma)
  • Swelling
  • H/O Trauma
  • Neurological symptoms:
    • Pressure on nerve / stretching the nerve
  • Pathological fracture: minor trauma / strange fracture line

Clinical Examination

  • A mass (lump):
    • Location
    • Discrete (separated) or ill-defined
    • Tenderness
    • Temperature
    • Pulsatile
    • Mobility
    • …etc
  • Range of motion
  • LN, pelvis, abdomen, chest, spine

Diagnostic Approaches

Imaging Studies

X-rays

  • Which bone, and which site in bone?
  • Solitary or multiple?
  • Bone forming or bone eating?
  • Margins: well-defined or ill-defined?
  • Calcifications in the lesion?
  • Is cortex eroded or destroyed?
  • Is there periosteal new bone formation?
  • Soft tissue extension?

Note: Shall be discussed separately

Other Imaging Modalities

  • Bone scan ():
    • Shows the site of lesion / skip lesions / metastasis
  • CT:
    • Shows Intra and extra-osseous structure and extension
    • Good in deep bones (pelvis, spine)
  • MRI:
    • Tumor spread:
      • Within bone, into joints, into soft tissue
      • Relation to vessels
      • Soft tissue and cartilage tumors

Laboratory Investigations

  • Look for infection:
    • CBC, differ WBC, CRP, blood c/s
  • Look for metabolic disease:
    • Brown tumor in hyperparathyroid disease
  • Anemia, raised ESR
  • S. Alkaline phosphatase
  • Tumor markers:
    • Bence Jones protein in urine: Myeloma
    • S. Acid phosphatase & PSA: Prostatic carcinoma
  • Raised serum Calcium in metastasis

Biopsy

  • Diagnostic
  • Needle biopsy:
    • CT-guided
    • In the line of further surgical incision
  • Open biopsy:
    • After all imaging techniques completed
    • More reliable
    • Site: considering further surgery
    • From boundaries

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Jamshidi needle


Differential Diagnosis

Soft Tissue and Traumatic Conditions

  • Soft tissue hamartomas
  • Myositis ossificans
  • Stress fracture:
    • Histopathology may be confused with osteosarcoma?
  • Tendon avulsion injuries:
    • Near hip and knee (e.g. Osgood-Schlatter)
  • Infection

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Metabolic and Other Bone Lesions

  • Hyperparathyroid disease (Brown tumor)
  • Gout: Large gouty typhus
  • Other bone lesions:
    • Cortical defects, bone infarcts, “bone islands”

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