MSK Patho UE Flashcards
DJD/OA are characterized by
- Degeneration of articular cartilage with hypertrophy of subchondral bone & joint capsule of weight bearing joints
- Most common form of arthritis affecting men more than women before age 50 and women more than men after age 50
- Slowly progressive condition
Signs and symptoms of DJD/OA
- Pain
- Swelling
- Loss of ROM
- Bony deformity
Radiographic findings indicating OA
- Diminished joint space
- Decreased height of articular cartilage
- Presence of osteophytes
- Subchondral cysts
Primary medications used for management of DJD/OA
- Oral analgesics
- NSAIDs
- Corticosteroid injections
- Viscosupplementation or intra-articular injections of the knee with a form of hyaluronic acid can be used
Pathology of Ankylosing spondylitis
- Progressive inflammatory disorder of unknown etiology that initially affects axial skeleton
- HLA-B27 biomarker indicating disease
Timeline of symptoms for Ankylosing spondylitis
- Mid to LBP for ≥3 months before the 4th decade of life
- Morning stiffness and sacroiliitis
- Results in kyphotic deformity of cervical/thoracic spine & decreased lumbar lordosis
- Men affected 3x more than women
Medications used for management of Ankylosing spondylitis
- NSAIDs to reduce inflammation & pain
- Corticosteroids to suppress immune system to control various sx
- Cytotoxic drugs (drugs that block cell growth) for those that don’t respond well to other treatments
- Tumor necrosis factor (TNF) inhibitors to improve some sx
Pathology of Gout
- Genetic disorder of purine metabolism
- Characterized by elevated serum uric acid (hyperuricemia)
- Uric acid changes into crystals & deposits into peripheral joints & other tissues
What joints is Gout most frequently observed
- Knee
- Great toe
Medications for management of Gout
- NSAIDs
- COX-2 inhibitors
- Colchicine
- Corticosteroids
- Adrenocorticotropic hormone (ATCH)
- Allopurinol
- Probenecid
- Sulfinpyrazone
Pathology of Psoriatic arthritis
- Chronic, erosive inflammatory disorder of unknown etiology, associated with psoriasis
- Both sexes affected equally
- Erosive degeneration typically of the digits and axial skeleton joints
Medications for management of Psoriatic arthritis
- Acetaminophen for pain
- NSAIDs
- Corticosteroids
- DMARDs (disease modifying anti rheumatic drugs) to slow progression
- Biological response modifiers (BRM) like Enbrel
Pathology of RA
- Chronic systemic autoimmune disorder of unknown etiology thought to have a genetic basis
- Pts produce antibodies to their own immunoglobulins (RF and ACPA)
- Characterized by periods of exacerbation and remission
Who does RA affect
- Women affect 2-4x more than men
- Age of onset ~40-60
- Onset may be gradual or abrupt
How is RA characterized
- Bilateral and symmetrical synovial joint involvement
- Most common joints include hands, feet, and cervical spine
- Systemic features may include weight loss, fever, and extreme fatigue
Diagnostic testing for RA
- Radiographs
- Increased white blood cell count
- Increased erythrocyte sedimentation rate
- Elevated rheumatoid factor
- Hemoglobin and hematocrit will show anemia
Medications for management of RA
- Golds and DMARDs in early stages
- NSAIDs and immunosuppressive agents
- Corticosteroids for acute flare-ups or long term management
Pathology of osteoporosis
- Metabolic disease that depletes bone mineral density/mass, predisposing individual to fracture
- Affects women 10x more than men
Common fracture site for osteoporosis
- Thoracic and lumbar spine
- Femoral neck
- Proximal humerus
- Proximal tibia
- Pelvis
- Distal radius
What is primary/postemenopausal versus senile osteoporosis
- Primary: directly related to a decrease in estrogen production
- Senile: occurs due to a decrease in bone cell activity secondary to genetics or acquired abnormalities
Medications for management of osteoporosis
- Calcium
- Vitamin D
- Estrogen
- Calcitonin
- Biophosphonates
Pathology of osteomalacia
- Decalcification of bones due to vitamin D deficiency
- Sx: severe pain, fractures, weakness, deformities
Medications for management of osteomalacia
- Calcium
- Vitamin D
- Vitamin D injections in the form of calciferol (vitamin D2)
Diagnostic tests for osteomalacia
- Radiographs
- Urinalysis and blood tests
- Bone scan
- Bone biopsy if warranted
Pathology of osteomyelitis
- Inflammatory response within bone caused by an infection
- Usually caused by Staphylococcus aureus
- More common in children and immunosuppressed adults
- More common in men than women
Treatment for osteomyelitis
- Antibiotics
- Proper nutrition
- Surgery if infection spreads to joints
Pathology of myofascial pain syndrome
- Characterized by “trigger point” which is a focal point of irritability found within a muscle
- Trigger point can be identified as a taut, palpable band within the muscle
Difference between an active versus latent trigger point
- Active: tender to palpate & have a characteristic referral pattern of pain when provoked
- Latent: palpable taut bands that are not tender to palpate but can be converted into an active trigger point
Medical intervention for trigger points
- Dry needling
- Analgesic injection
- Can be combined with a corticosteroid
Pathology of tendonosis/tendonopathy
- Dysfunction caused by an imbalance between tendon loading and recovery which leads to tendon failure an a microscopic and eventually macroscopic level
Histological characteristics of tendonosis/tendonopathy
- Hypercellularity
- Hypervascularity
- No indication of inflammatory infiltrates
- Poor organization and loosening of collagen fibrils
Pathology of bursitis
- Inflammation of bursa secondary to overuse, trauma, gout, or infection
Signs and symptoms of bursitis
- Pain with rest
- PROM and AROM are limited due to pain but not in a capsular pattern
Medications for management of bursitis
- Acetaminophen
- NSAIDs
- Steroid injections
Pathology for muscle strains
- Inflammatory response within a muscle following a traumatic event that caused microtearing of the musculotendinous fibers
- Pain and tenderness within that muscle
- Pain with active contraction and passive stretch of the muscle
Pathology of myositis ossificans
- Painful condition of abnormal calcification within a muscle belly
- Usually precipitated by direct trauma that results in hematoma and calcification of the muscle
What are the most frequent locations for myositis ossificans
- Quadriceps
- Brachialis
- Biceps brachii
When is surgery warranted for management of myositis ossificans
- Only in pts with non-hereditary form
- Only after maturation of the lesion (6-24 months)
- Indicated when lesion mechanically interferes with joint movement or impinge on nerves