A 38-year-old woman sought treatment with cranio-facial dysplasia involving
the cranium, maxilla and the mandible, Her chief complaint was a mandibula
r swelling, which had appeared about 2 years previously, had gradually enla
rged, and was associated with spontaneous pain. X-ray film examination reve
aled a ground-glass opacity with blurred demarcation and a 99 Tc medronate
bone scan disclosed an increase in tracer uptake in the cranium, maxilla an
d mandible. The rest of the skeleton was not affected. Histological examina
tion of the lesions revealed solid proliferation of spindle-shaped cells as
sociated with islands of osteid and bone trabecullae with Chinese letter pa
ttern and numerous multinucleated giant cells consistent with fibrous dyspl
asia, The continued osteoblastic activity of involved bones, coupled with t
he medical condition of the patient, restricted the management of the patie
nt to largely supportive and palliative care.