OncologyOncology

GCT Recurrence After BKA

Oncology
Advanced
6 min
High Yield
giant cell tumourGCT recurrencebelow knee amputationdenosumablung metastaseslocal recurrenceCampanacci classificationcurettagewide resectionprosthesis infection
6:00
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GCT Recurrence After BKA with THR

Clinical Scenario

A 38-year-old male presents with 3 months of worsening left knee pain at night. He had a left below-knee amputation (BKA) 15 years ago for a giant cell tumour (GCT) of the distal tibia. He subsequently developed symptomatic osteoarthritis of the left knee and underwent total hip replacement on the left 18 months ago. He is otherwise fit and well.

History:

  • Left distal tibia GCT diagnosed age 23
  • Treated with extended curettage, high-speed burr, phenol, cement
  • Recurred twice over 5 years
  • Eventually required BKA at age 28
  • Left THR 18 months ago for hip OA (presumed gait-related)
  • Now 3-month history of:
    • Left knee pain (residual limb)
    • Worse at night
    • Mild swelling above BKA stump
    • No constitutional symptoms

Examination Findings:

  • Below-knee amputation stump, well-healed
  • Mild swelling in distal thigh/knee region
  • Tenderness over medial femoral condyle
  • No warmth or erythema
  • THR scar well-healed
  • Hip ROM: Full and painless
  • Knee (prosthetic): Not assessed
  • No palpable lymphadenopathy
  • Chest clear

Investigations

Laboratory Results

Imaging

Plain X-ray Left Femur/Knee:

  • BKA stump with tibial remnant
  • THR in situ, appears well-fixed
  • Lytic lesion in left medial femoral condyle, 4 x 3 cm
  • Geographic pattern with narrow zone of transition
  • No periosteal reaction
  • No matrix calcification
  • Cortical thinning but no pathological fracture

MRI Left Femur:

  • 4.2 x 3.5 x 3.0 cm lesion in medial femoral condyle
  • T1: Intermediate signal
  • T2: Heterogeneous high signal
  • Gadolinium: Solid enhancement
  • No soft tissue extension
  • No skip lesions
  • Clear of THR stem

CT Chest:

  • 3 pulmonary nodules identified:
    • Right lower lobe: 12mm
    • Right middle lobe: 8mm
    • Left lower lobe: 6mm
  • No mediastinal lymphadenopathy
  • Concerning for pulmonary metastases

Bone Scan:

  • Increased uptake in medial femoral condyle
  • No other skeletal lesions

Questions & Model Answers

Q

What are the differential diagnoses for this lytic lesion, and what is the most likely diagnosis?

Q

Describe the Campanacci grading system for GCT and how it guides treatment.

Q

How do you manage the pulmonary nodules in this patient with GCT?

Q

What is the role of denosumab in GCT management?

Q

What surgical treatment would you recommend for the femoral lesion?

Q

What is the prognosis and follow-up plan for this patient?


Key Teaching Points

ConceptDetail
GCT Recurrence15-25% after curettage, can occur years later
Lung Metastases2-3%, 'benign pulmonary implants', often indolent
Campanacci GradingI/II = curettage; III = consider wide resection
Recurrent GCTTreat more aggressively than initial presentation
DenosumabRANK-L inhibitor, effective but rebound on cessation
PrognosisGood even with lung mets (>75% 5-year survival)

Common Examiner Follow-up Questions

  1. "What adjuvants can be used after curettage?"

    • High-speed burr (mechanical)
    • Phenol (chemical cautery)
    • Hydrogen peroxide
    • Liquid nitrogen (cryotherapy)
    • Argon beam coagulation
    • PMMA cement (thermal necrosis at cement-bone interface)
  2. "Why use cement instead of bone graft?"

    • Thermal necrosis at cement-bone interface may kill residual tumour cells
    • Easier to detect recurrence on X-ray (lytic line at cement-bone interface)
    • Immediate structural support
    • Bone graft: better for young patients, small defects, away from joint
  3. "What is the rebound effect with denosumab?"

    • Rapid tumour regrowth after stopping denosumab
    • Can occur within months of cessation
    • Tumour may be more aggressive than before treatment
    • Must plan surgery or ongoing treatment before stopping
    • Some advocate lifelong treatment for unresectable disease