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Giant cell
tumour of
bone
Dr Abdul G Suhail
MBBS,D.Ortho,MS (Ortho)

Assistant Professor in Orthopaedics
History




First described in 1818 by
Sir Astley Cooper
Described in detail in 1940
by Jaffe and Litchenstein
GIANT CELL TUMOUR

DEFINITION:

Distinct neoplasm arising from non-bone
forming supportive connective tissue of
marrow with network of stromal cells regularly
interspersed with giant cells.
( Jaffe & Liechtenstein )
AGE OF PRESENTATION
75-80% OF PATIENTS 20-50
YRS
 10% 15-20 YRS




10% >60 yrs



<1.7% BELOW 15 YRS
SEX




Male:Female- 1:1.3 (Benign)
-3:1 (Malignant)
SITE
Epiphyseo-metaphyseal
region of long bones



GCT –Described from all bones
EXCEPT middle ear bones
Axial skeleton- 8%
UL:LL-1:3
Site


55% AROUND THE KNEE



10% in the distal radius



6% in the proximal humerus





SPINE rarely involved (commoner in the
sacrum)
In the head and neck region the maxilla and
mandible are more commonly involved
GIANT CELL TUMOUR
INTRA ARTICULAR EXTENSION- 10%
TRANS OSSIOUS EXTENSION- 5%
Common sites
Wrist
Ankle & foot
Forearm
Leg
MULTICENTRIC INVOLVEMENT




Incidence-0.5-5%
Simultaneous
Peculiar features



hand
metaphyseal
abundant spindle
cells



GOLTZ syndrome
`
occular defects
skeletal anomaly
multifocal GCT
GIANT CELL TUMOUR

SIGNS&SYMPTOMS
1. PAIN
2. SWELLING
3. JOINT RESTRICTION
4. MUSCLE WASTING
5. NEUROLOGICAL SIGNS
6. PATHOLOGICAL #
Pathology
GROSS End of bone is expanded.
 Eccentric lesion at the epiphyseometaphyseal region.
 Thin periosteum.
 Fleshy dark brown, soft, friable
mass.
 Cystic spaces seen.
PATHOLOGY
GROSS-
Pathology
Microscopy

Vascularized network of round,oval or
spindle shaped stromal cells and
multinucleated giant cells with numerous
centrally placed nuclei
PATHOLOGY
MICROSCOPY
Grading
Jaffe,Lichenstein and
Portis(1940)
GRADE 1o Conventional GCT
o Stroma is inconspicuous
o Giant cells dominate the field
o No atypism of stromal cells and are
loosely arranged
o Stromal cells are predominantly
spindle shaped
Grading
GRADE 2o Boderline tumours
o Stromal cells are prominent and tightly
packed
o Giant cells are less in number compared to
grade 1 and their nuclei may show
atypism
o Stromal cells show atypism
o These tumours have a strong chance for
recurrence and some may undergo
malignant change
Grading
GRADE 3o Sarcomatous type of stroma
o Frequently metastase
o Stromal cells abundant and closely
compacted and present an irregular
whorled arrangement
o Nuclei are unusually large, irregular and
atypical
o Giant cells are few in number and atypical
Modified grading
Sannerkin et al(1980)






Malignant GCT- with frank
sarcomatous changes and full
metastatic potential
Borderline GCT- without sarcomatous
changes but with abnormal mitoses
or vascular permeation or both
Conventional GCT- without features
of any of the above two types
No correlation exists
between histological
grading and clinical
behavior of the tumour.
Hence grading not widely
accepted.
GIANT CELLS in
Giant cell tumor
 Numerous
nuclei(15-150)
 Centrally placed
uniform size nuclei

Tuberculosis
 Number of nuclei
are less
 Peripherally placed
nuclei
Enneking staging for GCT
Stage 1-(10-15%)







Patients asymptomatic
Discovered incidentally
May cause pathological fracture
Has sclerotic rim on x-ray or CT
Relatively inactive on bone scans
Histologically benign
Enneking staging for GCT
Stage 2-(70%)






Symptomatic
Often associated with path: fracture
Has expanded cortex but no break through
Is active on bone scans
Histologically benign
Enneking staging for GCT
Stage 3-(10-15%)










Symptomatic
Rapidly growing mass
Has cortical perforation with
accompanying soft tissue mass
Activity on bone scan extends beyond
the lesion in x ray
Shows intense hypervascularity on
angiogram
Histologically benign
RADIOLOGY
Type of Osteolysis



Geographic destruction (I)
Lodwick

1A



1B

Moth-eaten (II)

1C

Permeative(III)
RADIOLOGY


Expansile
RADIOLOGY


TRABACULATION

PURE LYTIC (60%)

FINE TRABACULTION(40%)
RADIOLOGY
AGGRESSIVENESS

LARGE INTRAOSSEOUS CONTENT
PURELY LYTIC
CORTICAL BREACH
SOFT TISSUE INVASION
INVESTIGATIONS
SCINTI GRAPHY
Less useful
Inconsistent uptake
“Doughnut sign”

ANGIO GRAPHY
Locate vessels
type of feeders
For embolisation

C.T
Intraossous content
Intra articular spread
Cortical breach
Site of window

M.R.I.
Soft tissue spread
Joint breach
Locate N.V. bundle
GCT Ulna
GCT of Olecranon
GCT Radius
GCT distal femur
GCT lower end femur
GCT Fibula
GCT Calcaneum
GCT Ilium
GCT C7
DIFFERENTIAL DIAGNOSIS
1.ANEURYSMAL BONE CYST
2. GIANT CELL REPARATIVE GRANULOMA
3.CHONDROBLASTOMA
4.BROWN TUMOR
5.INTRA OSSEOUS GANGLION
6.BENIGN FIBROUS HISTEOCYTOMA
Bubbly lesions of bone
Tumors

Aneurismal bone cyst

Unicameral bone cyst

Non ossifying fibroma

Osteoblastoma

Hyper parathyroidism

Chondromyxoid fibroma

Histiocytosis X

Myeloma

Metastasis(kidney,thyroid)
Infection

Brodies abscess

Coccidioidomycosis

Ecchinococcus
BIOPSY
CLOSED

FINE NEEDLE
TRUECUT
TREPHINE

OPEN

INCISIONAL
EXCISION
TREATMENT
STAGE

STAGE1

TYPE

LATENT
Lodwick2
STAGE 2 ACTIVE
Lodwick3
STAGE 3 AGGRES.

GRADE

SITE

METASTASIS

G0

T0

M0

G0

T0

M0

G0

T1,2

M0,1
SURGICAL TREATMENT
Stage1& Stage2 --- Intralesional or Marginal Excision
Stage3 --- Wide resection with Reconstruction
Radiation, Embolaisation
Curettage & Bone Grafting
INDICATION STAGE-1&2
ADEQUATE WINDOW
MOTORISED BURR
Extended Curettage
PHENOL
BONE CEMENT
LIQUID NITROGEN
CAUTERY
CO 2 LASER
EN.BLOC EXCISION
 Better result
 Dispensable bone ---- Patella, head of Fibula
 Sub articular lesion
RECONSTRUCTION





Auto graft
Allograft
Arthrodesis
Custom made prosthesis
Reconstruction With
Autograft
Reconstruction With
Allograft
Reconstruction With
Arthrodesis
Reconstruction With Prosthesis
Metastasis
Benign pulmonary metastasis seen in 2% of patients
unpredictable course
Some spontaneously regress
Others treated by pulmonary wedge resection
25% mortality
Other sites
Lymph nodes, mediastinum ,pelvis.
Pushpavally 32yrs
Pushpavally 32yrs
FEMALE 21YRS.

15-5-92
Lady 28yrs.
Recurrent GCT
Recurrent GCT
Recurrent GCT
Recurrent GCT
Recurrent GCT
Recurrent GCT

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