Abstract
Fibrous dysplasia is a benign bone disorder. It is diagnosed by distinctive X-ray radiography, CT, and MRI findings. Although bone scintigraphy helps to identify the tumor origin according to accelerated bone turnover, the glucose metabolism in fibrous dysplasia has not yet been investigated. We reported a case of fibrous dysplasia in craniofacial bone which showed signs of the acceleration of bone mineral turnover without elevated glucose utilization by Technetium-99m-HMDP SPECT and Fluorine-18-FDG PET. We concluded that the growth of fibrous dysplasia needed the acceleration of bone mineral turnover without an increase in glucose metabolism.
MeSH terms
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Bone Density
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Facial Bones* / diagnostic imaging
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Facial Bones* / pathology
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Female
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Fibrous Dysplasia, Polyostotic / diagnostic imaging*
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Fibrous Dysplasia, Polyostotic / metabolism*
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Fluorodeoxyglucose F18 / pharmacokinetics*
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Glucose / metabolism
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Humans
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Hyperplasia
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Middle Aged
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Radiopharmaceuticals / pharmacokinetics
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Sclerosis
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Skull* / diagnostic imaging
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Skull* / pathology
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Technetium Tc 99m Medronate / analogs & derivatives
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Tomography, Emission-Computed, Single-Photon
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Tomography, X-Ray Computed
Substances
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Radiopharmaceuticals
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Fluorodeoxyglucose F18
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technetium Tc 99m hydroxymethylene diphosphonate
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Glucose
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Technetium Tc 99m Medronate