Giant cell tumour

on 2.7.06 with 0 comments



Osteoclastoma is a locally aggressive (osteolytic) neoplasm found most often in the epiphyseal ends of long bones (>75% in articular end of long bone) in adults 20-55 years. More than half occur about the knees, but virtually any bone can be involved. Giant cell tumour of bone is rare in the skeletally immature people and infrequent in the elderly.

Morphology of osteoclastoma: laboratory and biopsy findings…

Histologic pattern is one of:

  • Many uniformly distributed osteoclast-like, multinucleated giant cells in a plump spindle cell background (mononuclear cell population)

[The neoplastic cell is the spindled stromal cell; the multinucleated cells are thought to arise from fusion of the spindle cells.]


There may be foci of necrosis, haemorrhage, hemosiderin or osteoid.

Macroscopic and radiologic appearances are distinctive (not pathognomonic):

  • Imaging may reveal large lytic soap-bubble lesions; absent are stippling and calcifications.

  • Classically lucency presentation epiphyseal in location (femur, tibia & radius) definition (though may extend to involve the metaphysis), subchondral and eccentrically located to long axis of bone.

  • Cortical expansion and focal destruction may be observed, sometimes with extension into overlying soft tissues (20%).


Histologic features do not allow prediction of which tumours will recur or metastasize. A rare lesion is overtly malignant from the outset.


This biologic unpredictability complicates clinical management:

  • Majority of tumours are localized and can be eradicated by curettage or conservative resections

  • 40-60% recur locally

  • 1-2% develop deceptively benign-looking metastases to the lungs

  • ~10% develop obviously anaplastic metastases

Category: Orthopedics Notes , Pathology Notes

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