2. Skeletal System - Pathologies Flashcards
Fractures
Any break in a bone
Causes include trauma, low bone density (osteoporosis), vitamin D deficiency
Types of Fractures
Complete - bone is broken in two of more fragments
Incomplete - not in fragments
Avulsion - tendon or ligament pulls off a piece of bone
Fracture repair
- Haematoma (& inflammation): Blood vessels at fracture line are broken and blood leaks into site. Causes death of local cells and swelling.
- Fibrocartilaginous callus formation: Phagocytes clean up the debris. Fibroblasts invade & lay down collagen forming a ‘soft callus’ (2-3 weeks).
- Bony callus formation: Osteoblasts replace cart with new bone(<3 months).
- Bone remodelling:The callus is mineralised & compact bone laid down. Then Osteoclasts reshape the new bone. Remodelling occurs over months to years.
Sprains
Involve a trauma that fores a joint beyond its normal range, over-straining / tearing ligaments
Subluxation
Incomplete or partial joint dislocation
Dislocation
Complete separation of the two bones at a joint
Kyphosis
Rounding of the upper back.
Lordosis
Increased concavity in the lumbar and cervical spine
Scoliosis
A lateral S-shaped curve in the spine
Osteoporosis
Chronic, progressive thinning of the bone (porous bone).
Characterised by decreased bone mineral density leading to bone fragility & and an increased risk of fracture
Diagnosed by ‘Dual X-Ray Absorptiometry’
Osteoporosis: Risk Factors
Increasing age -> over 30 Female and post-menopausal Poor diet Drugs -> long term corticosteroid therapy GIT diseases Genetics Sedentary lifestyle Endrocrine pathologies (Cushings, hyperparathyroidism) Low body weight High alcohol consumption and smoking Toxins (heavy metals)
Osteoporosis: Signs & Symptoms
Fractures with minor trauma
Focal pain and kyphotic posture with loss of height
Pain is aggravated by prolongued sitting, standing or bending, relieved by lying on side with hips & knees flexed
Osteorporosis: Treatment
Bisphosphonates (AledronicAcid)
HRT
Osteomalacia and Rickets
Inadequate mineralisation of the bone matrix in spongy and compact bone.
Softening of bone
Rickets - prior to epiphyseal plate closure >18yo
Osteomalacia - as adult or adolescent
Osteomalacia and Rickets: Causes
Vitamin D deficiency, possibly due to:
• Insufficient sunlight.
• Insufficient dietary vitamin D.
• Secondary deficiency: malabsorption disorders.
•Reduced receptor sites for vitamin D in tissues
Osteomalacia and Rickets: Signs and Symptoms
- Deformed bones (bowed legs) & possible fractures.
- Severe back pain & muscle weakness.
- In Rickets:Delayed closure of fontanelles and skull softening.
Osteomyelitis
A bacterial infection of the bone marrow, resulting in necrosis and hence bone weakness.
Diagnosed by
• Bloods: Elevated inflammatory markers(ESR/CRP) & WBC’s.
• X-ray, MRI.
Osteomyelitis: Causes
- Bacterial infection(staphylococcus aureus) through the blood supply or post-fracture.
- Immunosuppression, diabetes, IV drug users.
Osteomyelitis: Signs and Symptoms
Presents as severe bone pain (often worse at night), with swelling, redness and warmth.
Osteoarthritis
A degenerative wear & tear arthritis of the articular cartilage, typically affecting weight bearing (larger) joints in individuals typically over 50 years of age.
Osteoarthritis: Causes
• Primary:A ssociated with aging. 80% of 65 year old’s have radiological signs of OA.
• Secondary: Associated with predisposing factors:
Congenital ill-development.
Trauma –e.g. fractures, surgery, meniscal injury, obesity.
Osteoarthritis: Signs and Symptoms
- Onset is gradual, pain increasing (months –years).
- Joint pain and stiffness.
- Not associated with systemic symptoms.
Osteoarthritis: Pathophysiology
- Articular cartilage wears away; underlying bone is exposed.
- Subchondral bone becomes hard and glossy (‘eburnation’).
- Remodelling of underlying bone (i.e. thickening) occurs.
- Compensatory bone overgrowth in an attempt to stabilise joint = Osteophytes(spurs).
Rheumatoid Arthritis
Autoimmune inflammation of the synovium, potentially affecting ALL organs except the brain (systemic inflammation).
• Affects 1% of people worldwide, ↑ in women.
• Peak occurrence between 30–50 years of age