Bone scintigraphy proved valuable in diagnosing McCune-Albright's syndrome in a 6-year-old girl by detecting multiple, non-symptomatic foci in the skull, axial skeleton and in the extremities. Subsequent roentgen examination showed abnormal bone structure in the affected areas, consistent with fibrous dysplasia.
AlbrightF.ButlerA.HamptonA.SmithP.: Syndrome characterized by osteitis fibrosa disseminata, areas of pigmentation and endocrine dysfunction with precocious puberty in females. Report of five cases. New Engl. J. Med.216 (1937), 727.
2.
FitzerM.: Radionuclide angiography. Brain and bone imaging in craniofacial fibrous dysplasia (CFD). Case report. J. Nucl. Med.18 (1977), 709.
3.
GildayG.AshJ.: Benign bone tumors. Sem. Nucl. Med.6 (1976), 33.
4.
GrablasS.CampbellC.: Fibrous dysplasia. Orthop. Clin. N. Amer.8 (1977), 771.
5.
GreenfieldG.: Radiology of bone diseases. Third edition, p. 124. J.B. Lippincott Co., Philadelphia1980.
McCuneD.BruchH.: Osteodystrophia fibrosa. Report of a case in which the condition was combined with precocious puberty, pathologic pigmentation of the skin and hyperthyroidism, with review of the literature. Amer. J. Dis. Child.54 (1937), 806.
8.
SeniorB.RobboyS.: Case records of the Massachusetts General Hospital. Case 4–1975. New Engl. J. Med.292 (1975), 199.