Paget's Disease of the Bone Flashcards
Paget’s disease of the bone (PDB) is ______ in 1 or more bones due to abnormally large and overactive __ causing focal areas of excessive __, with compensatory __ at pagetic sites resulting in ______
Common symptoms (4)
Alternative name: __
Abnormal bone remodeling
Overactive osteoclast - excessive bone resorption
Compensatory bone formation by osteoblasts
Disorganised, enlarged, structurally weak bone
Symptoms:
- Bone pain
- Skeletal deformities
- Pseudofractures
- Osteoarthritis
Alternative name: osteitis deformans
Causes of PDB is unknon, but postulated:
- Genetic mutations in __ - encodes protein in osteoclast function
- __ infection - EM noted osteoclast intranuclear structures resembling nuclecaspids, though no virus cultured
SQSTM1 gene
Paramyxovirus
Epidemiology and clinical presentation of PDB
Middle age > 40 years old, increasing with age
Men > women
European > African and Asian
(US: 2-3% of population > 55 years)
- Asymptomatic, incidental findings
- Elevated ALP, abnormal XR of bones - Bone pain or osteoarthritis
- Deep aching, at rest or activity, worse at night - Skeletal deformities
- Enlarged skull (lion facies)
- Long bone deformity, tibial anterior bowing, femoral anterolateral bowing
- Subtle increased warmth (increased blood flow)
- Surgical scars for previous long bone fractures - Complications
- Hearing loss and use of hearing aid
- High output failure and hyperdynamic circulation (collapsing pulse)
- Cranial nerve compression (CN8, CN2, CN5, CN7)
- Spinal disease and vascular steal syndrome
Differential diagnosis of PDB
- Chronic osteomyelitis
- Fibrous dysplasia
- Metastatic disease to the bones
- Metaphyseal dysplasia (Engelmann’s disease)
- Hyperostosis frontalis interna
- Familial expansile osteolysis
- Osteosarcoma
- ALP elevation in liver or biliary disease
- Osteomalacia
- Hyperparathyroidism
- Multiple myeloma
What bones are involved in PDB?
Mono-ostotic or poly-ostotic
Predilection for axial skeleton, but can affect any bone
Number of skeletal sits involved stable over time, rarely developing new lesions after diagnosis
Commonest
1. Pelvis - 70%
2. Femur - 55%
3. Lumbar spine - 53%
4. Skull - 42%
5. Tibia - 32%
Triphasic progression of pagetic bone lesion
- Lytic phase - focal bone resorption
- Increased osteoclast activity - enlarged, multinucleated
- Bone loss ,wedge shaped resorption in long bones or circumscribed lytic lesions in skull - Intermediate phase - osteoblast and accelerated bone formation
- Disorgansied bone architecture (mosaic or woven) with mixed lytic/sclerotic phase
- Impaired bone strength, risk of fracture
- Bone appears enlarged, sclerotic, with bowing deformities, linear radiolucencies (pseudofracture), calvarium and cortical thickening, coarse trabeculae - Cold phase - reduced bone cell activity
- Persistent abnormal bone architecture, woven bone converted to dense lamellar bone
Investigations for PDB
Elevated ALP in normal vitamin D (excludes osteomalacia) Isotopic bone scan
Biochemical
1. ALP - normal in osteolytic phase, raised in osteoblastic
(To send bone specific ALP)
2. Calcium and albumin
3. Liver function test
4. Vitamin D
Imaging
5. Plain XR
6. Radionucleide bone scan
Management and treatment goals of PDB
- Adequate calcium and vitamin D levels
- Analgesia for pain control
- Biphosphonates if indicated (see separate card)
- IV zoledronate 5mg: achieves ALP normalisation 96% (75% reduction in ALP) - Calcitonin - less effective
- Denosumab - off label use with significant fractur risk and BMD on stopping
Treatment goals
1. ALP reduction, reaching nadir by 3-6 months
(Alternative markers: C-telopeptides, N-telopeptides, P1NP, BSALP)
- No data to support normalisation reduces long term complication risks
What are the indications for biphosphonate treatment in PDB?
- Symptomatic active PDB
- High risk of complications - fracture in weight bearing bones, nerve compression
- Before elective surgery - reduces hypervascularity and perioperative blood loss
- Hypercalcaemia with immobility
What are the side effects of biphosphonates?
- Osteonecrosis of jaw
- Atypical femoral fractures (subtrochanteric)
- Nephrotoxicity, esp if eGFR < 35
- Hypocalcaemia, worse in vit D deficiency
- Oesophagitis and dyspepsia
Complications of PDB
- Osteoarthritis
- Bone deformity
- Fracture and pseudofracture
- Hearing loss
- Ossicle ankylosis and narrowing of IAM
- Cochlear damage from bony overgrowth - Cranial nerve compression
- Spinal stenosis and radiculopathy
- Obstructive hydrocephalus - base of skull compression
- High output cardiac failure
- Hypercalcaemia
- Giant cell tumour or osteosarcoma
Risk of osteosarcoma in PDB
< 1% of all patients
Suspect in PDB with:
- Increasing bone pain and swelling, worse at night
- New mass
- New fracture at pagetic site
Investigations: MRI of specific site
Prognosis: poor (5 year survival 10%)
What are causes of tibial bowing?
- Paget’s disease of the bone
- Neurofibromatosis (pseudoarthrosis of tibia)
- Rickets
- Fibrous dysplasia
- Fibular hemimelia
- Trauma
- Congenital