Musculoskeletal Disorders
Introduction
·
The musculoskeletal system is a complex network
comprising bones, muscles, joints, ligaments, tendons, and cartilage.
·
Musculoskeletal disorders are a broad
group of diseases and injuries affecting the bones, muscles, joints, and
connective tissues.
·
They may be traumatic (fractures, injuries),
degenerative (arthritis, osteoporosis), infectious (osteomyelitis), metabolic
(rickets, gout), or autoimmune/neuromuscular (myasthenia gravis).
·
These disorders often impair mobility, cause
pain, and reduce quality of life.
·
It provides:
·
Support and shape
to the body
·
Protection
to vital organs (e.g., skull protects brain, rib cage protects heart/lungs)
·
Movement and locomotion
via interaction of bones, joints, and muscles
·
Mineral storage
(especially calcium and phosphate)
·
Hematopoiesis
(blood cell formation in bone marrow).
Definition:
A fracture is a break in the continuity of bone
due to trauma, pathological weakness, or stress.
Types:
- Closed
(simple) – bone breaks without piercing skin.
- Open
(compound) – bone pierces skin, high risk of
infection.
- Greenstick
– incomplete break (common in children).
- Comminuted
– bone shattered into multiple fragments.
- Impacted
– ends driven into each other.
- Pathological
– occurs in weakened bone (e.g., cancer, osteoporosis).
- Stress
fracture – due to repeated
stress/microtrauma.
Clinical Features:
- Pain,
swelling, deformity
- Loss
of function
- Crepitus
(grating sound)
- Abnormal
mobility
- Bleeding
in open fractures
Management:
- First
aid: Immobilization, bleeding control, splinting
- Definitive
treatment:
- Closed
reduction (manual realignment)
- Open
reduction and internal fixation (ORIF)
- External
fixation (pins, rods)
- Rehabilitation:
Physiotherapy, nutrition (calcium, vitamin D).
Definition:
Inflammatory disorders of joints leading to pain,
stiffness, swelling, and reduced mobility.
Types:
- Osteoarthritis
(OA):
- Degenerative
joint disease due to wear and tear of cartilage.
- Common
in weight-bearing joints (knees, hips, spine).
- Symptoms:
Joint pain, stiffness (worse after activity), crepitus, limited movement.
- Rheumatoid
Arthritis (RA):
- Autoimmune
disease causing chronic synovial inflammation.
- Symmetrical
joint involvement (small joints first – fingers, wrists).
- Symptoms:
Morning stiffness > 1 hr, swelling, deformities (ulnar deviation).
- Extra-articular:
nodules, vasculitis, lung fibrosis.
- Gouty
Arthritis:
- Deposition
of uric acid crystals in joints.
- Sudden
severe pain, redness, swelling (often big toe – podagra).
Management:
- Analgesics,
NSAIDs
- DMARDs
(e.g., methotrexate for RA)
- Corticosteroids
- Lifestyle:
weight control, physiotherapy, assistive devices.
Definition:
A metabolic bone disorder characterized by low bone
mass and micro-architectural deterioration, leading to fragile bones.
Causes/Risk Factors:
- Aging
(postmenopausal women due to estrogen deficiency)
- Sedentary
lifestyle, low calcium/vitamin D intake
- Prolonged
corticosteroid use
- Smoking,
alcohol
- Endocrine
disorders (thyroid, parathyroid abnormalities).
Clinical Features:
- Often
silent until fracture occurs
- Fragility
fractures (hip, vertebra, wrist)
- Stooped
posture (“dowager’s hump”)
- Loss
of height, back pain.
Management:
- Prevention:
Adequate calcium & vitamin D, weight-bearing exercise
- Treatment:
Bisphosphonates, SERMs (Raloxifene), Calcitonin, Hormone replacement
therapy (HRT).
Paget’s Disease (Osteitis Deformans)
Definition:
A chronic disorder of bone remodeling where there is excessive
bone resorption followed by disorganized bone formation, leading to
enlarged but weak bones.
Etiology:
- Exact
cause unknown
- Possible
viral infection in genetically predisposed individuals.
Clinical Features:
- Bone
pain, deformities (bowed legs, enlarged skull)
- Fractures
- Neurological
symptoms (hearing loss due to skull involvement).
Complications:
- Osteoarthritis
- Spinal
cord compression
- Rarely
osteosarcoma.
Management:
- Bisphosphonates,
Calcitonin
- Analgesics,
physiotherapy
- Orthopedic
correction of deformities.
Definition:
A metabolic bone disorder of children due to vitamin
D deficiency, leading to defective mineralization of bone.
Etiology:
- Inadequate
sunlight exposure
- Malnutrition,
malabsorption
- Chronic
renal/liver disease.
Clinical Features:
- Delayed
closure of fontanelles
- Bowed
legs (genu varum), knock knees (genu valgum)
- Rachitic
rosary (beading of costochondral junctions)
- Harrison’s
groove (depression of lower chest).
Management:
- Vitamin
D supplementation
- Adequate
calcium intake
- Sunlight
exposure
- Treat
underlying cause (renal/hepatic disease).
Definition:
A metabolic disorder caused by hyperuricemia
leading to deposition of monosodium urate crystals in joints and tissues.
Etiology:
- Overproduction
or underexcretion of uric acid
- Risk
factors: high purine diet, alcohol, obesity, renal disease.
Clinical Features:
- Sudden
severe joint pain (often at night)
- Swelling,
redness, warmth (esp. great toe – podagra)
- Tophus
formation (urate deposits in soft tissue)
- Kidney
stones, nephropathy.
Management:
- Acute
attack: NSAIDs, colchicine, corticosteroids
- Chronic:
Allopurinol, Febuxostat (lower uric acid levels)
- Lifestyle:
Avoid alcohol, red meat, organ meats; hydration.
Definition:
A chronic autoimmune neuromuscular disorder
causing weakness of skeletal muscles due to autoantibodies against
acetylcholine receptors at neuromuscular junction.
Clinical Features:
- Muscle
weakness that worsens with activity (fatigability)
- Ptosis
(drooping eyelids), diplopia (double vision)
- Difficulty
chewing, swallowing, speaking
- Weakness
of limb and respiratory muscles (myasthenic crisis).
Diagnosis:
- Tensilon
test (edrophonium improves weakness temporarily)
- Antibody
assays (AChR, MuSK antibodies)
- Electromyography.
Management:
- Anticholinesterase
drugs (pyridostigmine)
- Immunosuppressants
(corticosteroids, azathioprine)
- Thymectomy
if thymoma present
- Plasmapheresis,
IVIG (in severe crisis).
Definition:
An infection of bone and bone marrow, usually
caused by bacteria (most commonly Staphylococcus aureus).
Etiology:
- Hematogenous
spread (children)
- Direct
inoculation (fractures, surgery)
- Spread
from nearby infection.
Clinical Features:
- Acute:
Fever, chills, severe bone pain, swelling, redness, tenderness
- Chronic:
Sinus tract formation, persistent drainage, bone deformity.
Diagnosis:
- Blood
tests: raised ESR, CRP, leukocytosis
- Imaging:
X-ray (later changes), MRI (early detection)
- Bone
biopsy and culture.
Management:
- Prolonged
antibiotics (IV initially, then oral)
- Surgical
debridement of necrotic bone
- Drainage
of abscesses
- Supportive
care (nutrition, pain control).
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