case report gct

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    Multiple skeletal metastases

    from a giant cell tumour of

    the distal fibula with fataloucome

    CASE REPORT

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    Giant Cell Tumor of Bone

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    Definitionrare aggressive non-cancerous (benign) tumor

    potential for : recurrence metastasis

    Statistically :

    80% benign course, with a local rate ofrecurrence of

    20% to 50%.

    10% undergo malignant transformation atrecurrence

    1% to 4% give pulmonary metastases even incases of

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    Epidemiology

    5- 10% primary bone tumors

    20 % benign bone tumors

    F : M 1,5 : 1

    70- 80 % age 20 40

    higher incidence rates in Asia,

    20% of all primary bone

    tumors in China

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    Location

    usually prefers the

    epiphyses of long bones. half of the cases knee joint

    distal femur, proximal tibia,

    distal radius & proximal

    humerus.

    other sites: fibula, sacrum,

    & distal tibia

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    Diagnose

    History

    age

    progessivity of tumor

    pain swelling

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    Clinical symptom:

    hard and painfull mass

    swelling

    joint effusion

    tenderness, muscle atrofi

    patologic fractur (11-37%)

    neurogical deficit (sacrum)

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    Radiography :

    o lytic lession

    o radiolucent area at the end

    of the bone with no firmboundaries.

    o transition zone between

    normal and pathological

    bone

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    CT Scan :

    o improves detection

    of cortical thinning fracture,

    pathological, andperiosteal reaction.

    o to accurately determine

    the location and softtissue mass.

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    MRI

    o help determine extent of

    tumor destruction

    o indicated when the tumorhas eroded thorugh

    the cortex and allows

    determination of whether

    neurovascular structures

    are involved

    o help evaluate subchondral penetration

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    Angiography

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    Histology

    macroscopic : brown mass and soft

    haemorrhage and

    necrosis

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    microscopic :

    multinucleatedgiant cells

    mononuclear

    stroma (round /ovoid / spindle),

    large nuclei and

    indistinctnucleoli

    mitoses

    http://www.kumc.edu/instruction/medicine/pathology/ed/ch_26/c26_s41.jpg
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    Classification

    Enneking (radiological, histological and clinical

    classification) : stage I benign latent GCT (15%)

    stage II benign active GCT (70%)

    stage III

    locally aggressive tumors (15%) malignant sarcomatous lesion contiguous

    with benign

    GCT ( very rare)

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    Treatment

    Principal :

    Excise the lesion

    Sterilize the cavity

    Reconstruct the defect

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    Traditional

    Intralesional curettage & bone grafting

    Local recurrence rates 40-60%

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    Modern Adjuvant Treatment

    (Polymethylmethacrylate) PMMA

    Liquid N2

    Phenol

    Cryotherapy Irrigate cartilage

    Liquid nitrogen is a

    chemical reagent

    used in cryotherapy

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    Enbloc Resection reserved for expendable

    bones :

    prox fibula / distal ulna high recurrence with

    other Tx

    stage III lesions

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    Reconstruction

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    CASE REPORT in 1997

    A 25-year-old woman with no significant past medical historyunderwent curettage and grafting with spongiosa for a lesion at the

    lateral malleolus.

    Histological presence of a giant cell tumour.

    Malignancy was not suspected and recovery was uneventful.

    in April 2002

    the tumour recurred locally

    treated again with curettage and grafting.

    pathology laboratory : recurrent giant cell tumour

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    In Feb 2003

    recurrent pain in the lateral aspect of her right ankle

    radiographs progressive destruction of the distal fibula

    recurrence of the giant cell tumour.

    MRI a lesion in the distal fibula, 4 cm long and 3 cm wide.Extensive

    destruction of bone was localised to the area of the lateral malleolus.

    Tx : EN BLOCK RESECTION

    histology : giant cell tumor with mononucleal cell (spindle) with mild

    to moderat nuclear atypia and some mitosis

    3 month normal ankle and chest

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    in Nov 2003

    severe pain around the right iliac crest

    radiographs of the pelvic region, a whole body scan and a whole

    body CT scan, revealed multiple bony metastases.

    no abnormality was detected in the viscera or the lungs

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    Histology : recurrence of the giant cell tumour.

    Tx : chemotherapy with radiotherapy

    she developed signs and symptoms of raised

    intracranial pressure. Her condition deteriorated

    and she died in a state of epileptic shock.

    In the absence of a post-mortem examination it is

    not possible to be certain that there was no lunginvolvement.

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    DISSCUSSION

    In this case, the mechanism of tumour spread is unclear,

    particularly considering the lack of pulmonary metastases.

    One possible explanation might be retrograde embolisation via

    superficial veins.

    Vessel destruction within the tumour does not necessarily indicate

    a higher risk of metastases. About 40% of all GCT exhibit vessel

    destruction but very few of them develop metastases.

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    In this case, metastasis via the blood stream as

    seen in other malignant tumours has to be assumed.

    In this patient, passage through the lung without

    pulmonary cell colonisation may have occurred.

    giant cell tumours show a tendency to local

    recurrence

    Recurrences after the treatment mostly caused by

    curettage and can reach up to 85%.

    To suppress recurrence rate, curettage thermal

    cautery using 5% phenol, bone cement or with liquid

    nitrogen are recommended.

    In this way, the number recurrence after curettage

    action can be suppressed up to 20%.

    The most frequent recurrence occurred within a

    period of 2-3 years post surgery.

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    THANK YOU