The use of acrylic bone cement as an adjunct to surgical excision of g
iant cell tumour of bone appears to reduce the incidence of tumour rec
urrence. Possible mechanisms for this apparent tumour inhibition inclu
de cytotoxic effects from the methylmethacrylate monomer and tissue hy
perthermia from the heat of polymerization of the cement. This work pr
esents a method for the prediction of temperature fields and resulting
tissue necrosis arising from the implantation of polymethylmethacryla
te (PMMA) at the site of a curretted giant cell tumour of bone. This i
s accomplished using a two-dimensional model based on geometry obtaine
d from digitized MRI images of the distal femur. A general-coordinate,
non-orthogonal grid generation technique is used and solutions are ob
tained with an alternating-direction implicit (ADI) finite-difference
scheme. The nodal temperature histories are then used to evaluate the
effect of variable defect size on the zone of thermally induced cell n
ecrosis. The results suggest the depth of the necrotic region is quite
sensitive to the size of the implant. In at least some cases, the hea
ting effect is sufficient to cause significant necrosis of tumorigenic
cells. Implanting a large mass of acrylic may risk overkill, damaging
substantial amounts of healthy tissue.