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Ollier disease with digital enchondromatosis: anatomic and functional imaging
1From the Department of Radiology, Mayo Clinic, Scottsdale, AZ.
Clinical Nuclear Medicine
|October 25, 2013
Abstract:
Ollier disease is a rare skeletal disorder characterized by multiple enchondromas at metaphyseal regions of the bones. The disease is nonhereditary and usually the result of postzygote mutations during development. We present the features of digital enchondromatosis on bone scintigraphy, PET/CT, radiographs, and MRI in a patient, with a childhood diagnosis of Ollier disease.

