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Paget's disease

from Section I - Musculoskeletal radiology

Published online by Cambridge University Press:  22 August 2009

James R. D. Murray
Affiliation:
Bath Royal United Hospital
Erskine J. Holmes
Affiliation:
Royal Berkshire Hospital
Rakesh R. Misra
Affiliation:
Buckinghamshire Hospitals NHS Trust
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Summary

Characteristics

  • Sir James Paget described the disease in 1877 as a chronic inflammatory remodelling disease of bones. He labelled the condition osteitis deformans.

  • Characterised by bony thickening and enlargement secondary to increased bone turnover.

  • The bone is weak and brittle due to abnormal bone structure.

  • Unknown aetiology (possible link with paramxyovirus) occurring in approximately 3% of the population over 40.

  • Environmental and family clustering is seen – 7% males in Lancashire (north-west UK).

Clinical features

  • Pain is the commonest symptom, but most patients asymptomatic.

  • Monostotic or polyostotic.

  • Sarcomatous change within the abnormal bone is the most sinister complication – said to be 1%.

  • Other complications include pathological fractures, bony impingement on nerves and secondary arthritis.

  • Deafness may occur secondary to nerve impingement or involvement of the ossicles.

  • Frequently affected bones include the pelvis, lumbar and thoracic vertebrae, proximal femur, calvarium and tibia.

  • High-output heart failure is a rare complication.

Radiological features

  • Thickened coarse trabeculae with cortical enlargement.

  • Cyst-like areas during the lytic phase.

  • Skull – both tables are involved with diplopic widening. Well-defined lytic areas more common anteriorly. The bony texture resembles ‘cotton wool’.

  • Pelvis – ilio-pectineal line thickening. Trabecular coarsening.

  • Long bones – curved femur and tibia.

  • Spine – ‘ivory vertebrae’ (sclerotic in appearance) or ‘picture frame’ appearance seen secondary to peripheral trabecular thickening and a relatively radiolucent central portion of the vertebral body.

  • Bone scan – marked increased uptake in affected bones. May be normal in ‘burned out’ disease.

Management

  • Often directed towards symptomatic relief.

  • Drugs such as bisphosphonates (and calcitonin) suppress bone turnover.

  • Surgical treatment of complications such as pathological fractures and secondary arthritis. Nerve entrapment may respond to decompression.

  • Sarcomatous change generally has a very poor prognosis.

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Publisher: Cambridge University Press
Print publication year: 2008

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