Long-term follow-up of a patient with McCune-Albright syndrome by whole-body bone scan and SPECT.

A 13-year-old girl with McCune-Albright syndrome underwent serial whole-body bone scans five times over the past eight years to evaluate involvement of fibrous dysplasia. These studies demonstrated incremental extension of polyostotic fibrous dysplasia in the appendicular and axial skeleton and skull base with the passage of time.