Key Points
• Fewer than 5% of patients with Paget’s disease will undergo malignant transformation to a sarcoma.
• The risk of a patient developing a sarcoma is greater the more extensive the Paget’s disease and the longer the patient has been affected.
• Paget’s sarcoma may appear photopenic (“cold”) on bone scintigraphy against a background of increased activity from the surrounding pagetic bone.
• Not all malignancies arising in Paget’s disease are a sarcoma. Metastases, myeloma and lymphoma should be considered in the differential diagnosis.
• There is a rare recognised association between Paget’s disease and giant cell tumour of bone typically involving the skull and facial bones.
• The preservation of the normal hyperintense signal of marrow fat on T1-weighted MR images is typical of uncomplicated Paget’s disease in all its stages. The loss of this hyperintense signal is seen when complications arise, including tumour, occult fractures, etc.
• The worldwide prevalence of Paget’s disease in the population appears to be decreasing.
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Davies, A., Pluot, E., James, S. (2009). Tumour and Tumour-like Conditions Associated with Paget’s Disease of Bone. In: Davies, A., Sundaram, M., James, S. (eds) Imaging of Bone Tumors and Tumor-Like Lesions. Medical Radiology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-77984-1_29
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