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โข Giant cell tumour (GCT)
o Though generally classified as benign, it
tends to recur after local removal
o Pathology
n Microscopically, the tumour consists of
undifferentiated spindle cells, profusely
interspersed with multi-nucleate giant cells.
.(MCQ)
n The tumour stroma is highly vascular.
n These giant cells were mistaken as
osteoclasts in the past, hence the name
osteoclastoma. .(MCQ)
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o Clinical features
o seen commonly in the age group of 20-40
years i.e., after epiphyseal fusion.(MCQ)
o The bones affected commonly are those
around the knee i.e., lower-end of the femur
and upper-end of the tibia. .(MCQ)
o Lower-end of the radius is another common
site.
o The tumour is located at the epiphysis
.(MCQ)
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o Examination
o a bony swelling, eccentrically located at the
end of the bone.
o Surface of the swelling is smooth.
o There may be tenderness on firm palpation.
o A characteristic 'egg-shell crackling' is often
not elicited. .(MCQ)
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o Diagnosis
o GCT is one of the common cause of a solitary
lytic lesion of the bone,
o Characteristic radiological features of GCT
n A solitary, may be loculated, lytic lesion.
n Eccentric location, often subchondral
n Expansion of the overlying cortex (expansile
lesion).
n 'Soap-bubble' appearance โ .(MCQ)
โข the tumour is homogeneously lytic with
trabeculae of the remnants of bone traversing
it, giving rise to a loculated appearance.
13. SOLITARY
LYTIC BONE
LESION
Differential
Diagnosis
(Mnemonic =
FOGMACHIN
ES)
โข
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F = Fibrous Dysplasia
O = Osteoblastoma
G = Giant Cell Tumour
M = Metastasis / Myeloma
A = Aneurysmal Bone Cyst
C = Chondroblastoma
H =
Hyperparathyroidism(brown
tumours)/ Hemangioma
I = Infection
N = Non-ossifying Fibroma
E = Eosinophilic Granuloma /
Enchondroma
S = Solitary Bone Cyst
14. Multinucleated osteoclastic giant cells intermixed
throughout a spindle cell stroma
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15. Multiloculated lesion with a very characteristic appearance
(honeycomb-like pattern) (left);
Pure lytic lesion (right)
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o Treatment
o Wherever possible, excision of the tumour is
the best treatment.
o For sites like the spine, radiotherapy is done.
o Excision
o treatment of choice when the tumour affects
a bone whose removal does not hamper with
functions e.g., the fibula, lower-end of the
ulna etc. .(MCQ)
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o Excision with reconstruction:
o in tumours affecting the lower-end of femur,
the affected part is excised en bloc, and the
defect thus created made up by one of the
following methods.(MCQ)
n Arthrodesis by the Turn-o-Plasty procedure
n Arthrodesis by bridging the gap by double
fibulae
n Arthroplasty
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o Curettage with or without supplementary
procedures:
o Curettage alone has high recurrence rate.
o Supplementary procedures used with
curettage have been reported to reduce
recurrence.
n Cryotherapy.(MCQ)
โข Liquid nitrogen is used to produce a freezing
effect and thus kill the residual cells,
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n Thermal burning of the residual cells
using cauterization of the walls of the tumour
n Thermal effect of bone cement
โข cavity is filled with 'bone cement', which by
the heat it produces while setting, 'kills' the
residual cells.
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o Treatment of GCT at common sites.(MCQ)
o Lower end of femur - Excision with Turno-
Plasty
o Upper end of tibia - Excision with Turno-
Plasty
o Lower end of radius - Excision with fibular
grafting
o Lower end of ulna -Excision
o Upper end of fibula โExcision
o For fibular grafting ,proximal end of the
opposite fibula is preferred, since it matches
the lower end of radius in shape.
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o secondary osteosarcoma
n occurs in older age (45 years onwards).
n pre-malignant conditions that predispose
.(MCQ)
โข Paget's disease, multiple enchondromatosis
โข fibrous dysplasia,irradiation to bones
โข multiple osteochondroma
30. Primary osteosarcomas
o Age at onset:
n occur between the ages of 15-25 years
n commonest musculoskeletal tumour at that age.
.(MCQ) .
o Common sites of origin: in decreasing order of
frequency
n lower-end of the femur(most common site );
upper-end of the tibia; and upper-end of the
humerus.
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o Histologically, anaplastic mesenchymal
parenchyma with tumour cells surrounded by
osteoid.
o Clinical features:
o Pain
n usually the first symptom, soon followed by
swelling. .(MCQ)
n Pain is constant and boring
n becomes worse as the swelling increases in
size.
o Sometimes, the patient presents with a
pathological fracture.
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o Examination:
o The swelling is in the region of the
metaphysis.(MCQ)
o Skin over the swelling is shiny with prominent veins
o The swelling is warm and tender
o Margins of the swelling are not well-defined.
o Movement at the adjacent joint may be limited mainly
because of the mechanical block by the swelling.
o The tumour may compress the neurovascular
structures of the limb, and produce symptoms due to
that.
o Regional lymph nodes may be enlarged, but are
usually reactive.
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o X-ray shows the following features
o An area of irregular destruction in the
metaphysis
o cortex overlying the lesion is eroded.
o There is new bone fomation in the matrix of
the tumour. .(MCQ)
o Periosteal reaction:
n As the tumour lifts the periosteum, it incites
an intense periosteal reaction.(MCQ)
n The periosteal reaction in an osteosarcoma
is irregular, unlike in osteomyelitis where it
is smooth and in layers.(MCQ)
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o Codman's triangle: .(MCQ)
n A triangular area of subperiosteal new bone
is seen at the tumour-host cortex junction at
the ends of the tumour.
o Sun-ray appearance: .(MCQ)
n As the periosteum is unable to contain the
tumour, the tumour grows into the overlying
soft tissues
n New bone is laid down along the blood
vessels within the tumour growing
centrifugally, giving rise to a 'sun-ray
appearance' on the X-ray.
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o Serum alkaline phosphatase (SAP):
o It is generally elevated.(MCQ)
o it is of no diagnostic significance
o considered a useful parameter for follow up
of a case of osteosarcoma.
o A rise of SAP after an initial fall after tumour
removal is taken as an indicator of
recurrence or metastasis.
o Biopsy:
o An open biopsy is performed to confirm the
diagnosis.
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o Why is it important to know the extent of
involvement of the affected bone by the
tumour
o To plan amputation surgery: .(MCQ)
n The tumour may have slip areas in
the medullary cavities, and can result in
recurrence even after amputation
o To plan a limb saving operation: .(MCQ)
n In cases presenting early, a radical excision
of the tumour is being performed these days
(limb saving surgery), thus avoiding
amputation.
47. o Treatment of the tumour:
o Local control of tumor:
o Amputation remains the mainstay of treatment.
.(MCQ)
o It can be a. palliative amputation, performed for
advanced disease, aiming at pain relief and a
better life.
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o Are the high amputations or disarticulations
through a joint proximal to the affected bone
are done now a days to avoid stump
recurrence?
n No, with the availability of effective
chemotherapy, stump recurrence can be
prevented even if the amputation is
performed through the affected bone,
provided it is performed taking a safe margin
beyond the tumour (usually 10 cm from the
tumour margin). .(MCQ)
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o Osteosarcoma - Level of amputation.(MCQ)
o Lower end of femur - Mid thigh amputation ,
Hip disarticulation
o Upper end of femur - Hip disarticulation,
Hindquarter amputation
o Upper end of tibia - Mid thigh amputation
o Upper end of humerus - Forequarter
amputation
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o Role of radiotherapy
o Radiotherapy is used for local control of the disease
for .(MCQ)
n tumours occurring at surgically inaccessible sites
n in patients refusing surgery.
o Routine pre-operative radiotherapy is no longer a
preferred method.
o Control of distant macro or micro-metastasis:
o In the majority of cases, micro-metastasis has
already occurred by the time diagnosis is made.
o These are effectively controlled by adjuvant
chemotherapy, immunotherapy etc.
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o A solitary lung metastasis may sometimes
be considered suitable for excision.
o Role of chemotherapy:
o It is given pre or post-operative
o micro-metastases at the time diagnosis can
be effectively controlled.
o drugs used are .(MCQ)
n high dose Methotrexate, Citrovorum factor
n Endoxan, Cisplatinum.
o A primarily lytic type (telangiectatic)
osteosarcoma has the worst prognosis
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โข Ewing's sarcoma
o highly malignant tumour
o occur between the age of 10-20 years.(MCQ)
o in two-third cases, occurs mainly in the femur and
tibia.(MCQ)
o About one-third of cases occur in flat bones, usually
in the pelvis and calcaneum. .(MCQ)
o diaphysis of the long bone is the most common site.
.(MCQ)
o bone may be expanded, and the periosteum
elevated, with sub-periosteal new
o bone formation, often in layers.
o The tumour ruptures through the cortex early, and
extends into the soft tissues.
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o The tumour grows fast and metastasizes
through the blood stream to the lungs and to
other bones.
o Clinical features:
o patient presents with pain and swelling.
o Often there is an associated fever, in which
case it may be confused with osteomyelitis.
.(MCQ)
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o Radiological features:
o In a typical case,
n lytic lesion in the medullary zone of the midshaft of a
long bone, with cortical destruction and new bone
formation in layers - onion-peel appearance .(MCQ)
o Atypical presentations
n tumour may be located in the metaphysis
n may be confused with osteomyelitis
n have a predominant soft tissue component with little
cortical destruction, and may resemble a soft tissue
sarcoma
n In flat bones, it is primarily a lytic lesion with hardly
any new bone formation.
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o Treatment
o highly radio-sensitive tumour.(MCQ)
o melts quickly but recurs.
o In most cases, distant metastasis has
occurred by the time diagnosis is made.
o Treatment consists of
n control of local tumour by radiotherapy (6000
rads)
n control of metastasis by chemotherapy