Paget's disease of bone (patient information)
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Paget's disease of bone |
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Paget's disease of bone On the Web |
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Risk calculators and risk factors for Paget's disease of bone |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Paget's disease is a disorder that involves abnormal bone destruction and regrowth, which results in deformity.
What are the symptoms of Paget's disease of bone?
- Bone pain (may be severe and persistent)
- Bowing of the legs and other visible deformities
- Enlarged head
- Fracture
- Headache
- Hearing loss
- Joint pain or stiffness
- Neck pain
- Reduced height
- Skull deformities
- Warmth of skin over the affected bone
Note: Most patients have no symptoms.
What causes Paget's disease of bone?
The cause of Paget's disease is unknown, although it might have to do with genes or a viral infection early in life.
The disease occurs worldwide, but is more common in Europe, Australia, and New Zealand.
In people with Paget's disease, there is an abnormal breakdown of bone tissue, followed by abnormal bone formation. The new bone is bigger, but weakened and filled with new blood vessels.
The disease may only be in one or two areas of the skeleton, or throughout the body. It often involves bones of the:
- Arm
- Collar
- Leg
- Pelvis
- Spine
Who is at highest risk?
The cause of this disease is unknown, therefor the risk factors are also unknown.
When to seek urgent medical care?
Call for an appointment with your health care provider if you develop symptoms of Paget's disease.
Diagnosis
Tests that may indicate Paget's disease include:
- Bone scan
- Bone x-ray
- Elevated markers of bone breakdown (for instance, N-telopeptide)
- Elevated serum alkaline phosphatase
This disease may also affect the results of the following tests:
- ALP (alkaline phosphatase) isoenzyme
- Serum calcium
Treatment options
Not all patients need treatment. For example, patients who have abnormal blood tests only may not need treatment.
People with Paget's disease who are commonly treated include:
- Patients with deformities
- Patients with no symptoms when certain bones (such as weight-bearing bones) are involved, especially if the bony changes are progressing quickly, to reduce the risk of fractures
- Patients with symptoms
Drug therapy helps prevent further bone breakdown. Currently, there are several classes of medications used to treat Paget's disease. These include:
Bisphosphonates -- These drugs are the first-line treatment, and they help increase bone density. Types of bisphosphonates include:
- Alendronate (Fosamax)
- Etidronate (Didronel)
- Pamidronate (Aredia)
- Risedronate (Actonel)
- Tiludronate (Skelid)
- Zoledronic acid (Zometa)
Calcitonin -- This hormone is involved in bone metabolism. Types include:
- Intranasal (Miacalcin)
- Subcutaneous (Calcimar)
Plicamycin (Mithracin)
Analgesics or nonsteroidal anti-inflammatory medications (NSAIDs) may also be given for pain.
Localized Paget's disease needs no treatment, if there are no symptoms and no evidence of active disease. Orthopedic surgery may be needed to correct a deformity in severe cases.
Where to find medical care for Paget's disease of bone?
Directions to Hospitals Treating Paget's disease of bone
What to expect (Outlook/Prognosis)?
Disease activity and symptoms can generally be controlled with current medications. A small percentage of patients may develop a cancer of the bone called osteosarcoma. Some patients will need joint replacement surgery.
Possible complications
- Bone fractures
- Deafness
- Deformities
- Heart failure
- Paraplegia
- Spinal stenosis