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180 Cards in this Set
- Front
- Back
Name all 8 Common Adult Orthopedic Injuries:
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shoulder dislocation, hip dislocation, colle's fracture, boxer's fracture, humerus fracture, "Night stick" fracture, monteggia's fracture
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Common Adult Orthopedic Injuries: what are the two types of Shoulder dislocation?
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Anterior Shoulder dislocation and posterior dislocation
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what is the most common shoulder dislocation?
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anterior dislocation
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Common Adult Orthopedic Injuries: Anterior shoulder dislocation presentation and what nerve and artery are involved?
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the axilliary nerve and artery are involved. Patient comes in holding the arm slightly abducted and externally rotated.
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Common Adult Orthopedic Injuries: Shoulder dislocation Tx. acute and recurrent dislocations
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reduction followed by a sling swath. Recurrent dislocations may need surgical repair
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Common Adult Orthopedic Injuries: Posterior dislocation of the shoulder is associated with what?
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seizure and electrocution
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Common Adult Orthopedic Injuries: Posterior shoulder dislocation injury: what artery and describe the presentation
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will injure the radial artery. Patients hold the arm in an adduction and internal rotation.
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Common Adult Orthopedic Injuries: 2 type of Hip dislocations
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anterior and posterior hip dislocations
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Common Adult Orthopedic Injuries: anterior hip dislocation can injure what nerve
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obturator nerve
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What is the most common hip dislocation?
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posterior hip dislocation
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Common Adult Orthopedic Injuries: Posterior hip dislocations is associated with what?
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sciatic nerve injury and avascular necrosis
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Common Adult Orthopedic Injuries: Posterior hip dislocations are common cause of what?
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It occurs via a "dash board injury". a posteriorly direct force on an internally rotated, flexed, adducted hip.
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Common Adult Orthopedic Injuries: Posterior hip dislocations Tx:
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closed reduction followed by abduction pillow/bracing. Evaluated with CT scan after reduction
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Common Adult Orthopedic Injuries: Colle's fracture association.
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commonly seen in the elderly (osteoporosis) and children
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Common Adult Orthopedic Injuries: Colle's fracture presentation
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It involves the distal radius. Often results from a fall onto an outstreched hand, leading to a dorsally displaced, dorsally angulated fracture
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Common adult orthopedic Injuries: Colle's fracture Tx:
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closed reduction followed by a long arm cast; open reduction if fracture is intrarticular.
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Common adult orthopedic Injuries: what is the most commonly injured carpal bone?
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scaphoid fracture
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Common adult orthopedic Injuries: how is Scaphoid fracture diagnosed?
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assume there is a fracture if there is tenderness on the anatomical snuff box. It may take 2 weeks for a radiograph to show the fracture.
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Common adult orthopedic Injuries: Scaphoid fracture Tx:
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thumb spica cast. If displacement or navicular or non-union is present do an open reduction.
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Common adult orthopedic Injuries: proximal third scaphoid bone fracture complication.
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AVN may result to disruption of blood flow
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Common adult orthopedic Injuries: Boxer's fracture presentation
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fracture of the fifth metacarpal neck due to a forward trauma of a closed fist (ie. punching a wall)
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Common adult orthopedic Injuries: Boxer's fracture Tx:
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close reduction and ulnar gutter splint. If fracture is excessively angulated: percutaneous pinning.
If skin is broken, assume infection: treat with surgical irrigation, debridment and IV antibiotics (covering eikenella) |
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what are the 6P's of compartment syndrome
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Pain
Pallor Paresthesias Poikilothermia Paralysis Pulselessness |
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complications of supracondylar fractures due to compartment syndrome
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Volkmann’s contracture of the
wrist and fingers. |
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what is compartment syndrome
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↑ pressure within a confined space that compromises nerve, muscle, and soft tissue perfusion.
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where is the most common location of compartment syndrome
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anterior compartment of the
lower leg and forearm. |
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presentation of compartment syndrome
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pain with passive motion
of the fingers and toes; paresthesias, pallor, poikilothermia, pulselessness, and paralysis. |
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how is compartment syndrome diagnosed?
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Measure compartment pressures (usually ≥ 30 mmHg); measure delta
pressures (diastolic pressure − compartment pressure). |
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treatment for compartment syndrome?
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Immediate fasciotomy to ↓ pressures and ↑ tissue perfusion.
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Risk factors for malignancy in lower back pain (6)
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1. age > 50,
2. a previous history of cancer, 3. pain not relieved by lying down 4. symptoms > 1 month, 5. pain that worsens at night 6. constitutional symptoms. |
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contraindicated in lower back pain
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Prolonged bed rest is contraindicated
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causes of herniated disk
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degenerative changes, trauma, or neck/back strain or sprain
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Most common area of herniated disk
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lumbar region, especially at L4–L5 and L5–S1.
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Dx and treatment: Bowel or bladder dysfunction, impotence, and saddle-area anesthesia
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cauda equina syndrome,
which is a surgical emergency |
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Hx and PE of herniated disk
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Sudden onset of severe, electricity-like LBP, usually preceded by several
months of aching, “discogenic” pain. ■ Common among middle aged and older men. ■ Exacerbated by straining (e.g., coughing). ■ Associated with sciatica, paresthesias, muscle weakness, atrophy, contractions, or spasms. ■ Passive straight leg raise ↑ pain (highly sensitive but not specific). ■ Large midline herniations can cause cauda equina syndrome. |
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what should be ordered is other lower back pain is suspected (ie. infection)
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plain radiograph if other causes of back pain are suspected
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what should be ordered if after conservative management of lower back pain, it would not resolve?
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MRI if symptoms are refractory to conservative management
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lower back pain treatment
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NSAIDs, physical therapy, and local heat → resolution within four weeks
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Tx: lower back pain with neurological symptom such a cauda equina.
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indications for discectomy.
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what is spinal stenosis?
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A narrowing of the lumbar or cervical spinal canal that can → compression of the nerve roots. usually due to degenerative joint disease in in middle-aged or elderly patients.
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spinal stenosis Hx/PE
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Neck pain; back pain that radiates to the buttocks and legs; leg numbness
and weakness. ■ Leg cramping is worse at rest, with standing, and with walking (pseudoor neurogenic claudication). ■ Symptoms improve with flexion at the hips |
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how is spinal stenosis diaganosed?
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Radiographs show degenerative changes and a narrowed spinal canal.
■ MRI or CT shows spinal stenosis. |
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Treatment of spinal stenosis:
mild to moderate |
Mild to moderate: NSAIDs and abdominal muscle strengthening.
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treatment of lumbar spinal stenosis: Advanced stage
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■ Advanced: Epidural steroid injections can provide relief.
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treatment of lumbar spinal stenosis: refractory stage
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■ Refractory: Surgical laminectomy may achieve significant short-term success,
but many patients will have a recurrence of symptoms |
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what is ankylosing spondylitis?
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A chronic inflammatory disease of the spine and pelvis that causes sacroiliitis
and, eventually, fusion of the affected joints. Strongly associated with HLAB27. Risk factors include male gender and a family history. |
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ankylosing spondylitis Hx/PE?
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Typical onset is in the late teens and early 20s
intermittent hip pain and LBP that worsen with inactivity and in the mornings but improve with activity. |
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ankylosing spondylitis Hx/PE II?
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↓ spine flexion ( +Schober test), loss of lumbar lordosis, hip pain and stiffness,
and ↓ chest expansion are seen as the disease progresses. ■ Anterior uveitis and third-degree heart block may occur. |
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what other diagnosis must be rule out in ankylosing spondylitis?
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Other seronegative spondyloarthropathies must be ruled out such as Reactive arthritis (aka Reiter’s syndrome) and Psoriatic arthritis
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Reiter’s syndrome
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disease of young men
arthritis, uveitis, conjunctivitis, and urethritis usually follow an infection with Campylobacter, Shigella, Salmonella, Chlamydia, or Ureaplasma |
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Psoriatic arthritis
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An oligoarthritis of the DIP joints. Associated with psoriatic skin changes and sausage-shaped digits.
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how is ankylosing spondylitis diagnosed
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+ HLA-B27.
Radiographs show bamboo spine and fused sacroiliac joints. ■ ESR ↑. ■ - RF; - ANA |
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treatment for ankylosing spondylitis: for pain, for improvement of posture and refractory cases
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NSAIDs (e.g., indomethacin) for pain; exercise to improve posture and breathing.
■ Tumor necrosis factor (TNF) inhibitors are used in refractory cases. |
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what is duchenne Muscular dystrophy and onset
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X-linked recessive disorder resulting from a deficiency of dystrophin, a cytoskeletal protein.
Onset is usually at 3–5 years of age. |
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Hx/PE: duchenne muscular dystrophy
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Affects axial and proximal muscles
progressive clumsiness, fatigability, difficulty standing or walking, difficulty walking on toes (gastrocnemius shortening), Gowers’ maneuver Pseudohypertrophy of the gastrocnemius muscles is also seen. ■ Mental retardation is common. |
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Dx of duchenne muscular dystrophy
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(-) dystrophin immunostain
↑ CK. ■ EMG shows polyphasic potentials and ↑ recruitment. Dystrophin mutation is sometimes seen. ■ Muscle biopsy |
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treatment of duchenne muscular dystrophy
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Physical therapy
Perform Achilles tendon release if necessary. |
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what would be the motor, sensory and reflex deficit if the nerve L4 is affected on a lower back pain?
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L4:
Motor: Foot dorsiflexion (tibialis anterior). reflex: Patellar sensory: Medial aspect of the lower leg. |
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what would be the motor, sensory and reflex deficiency if L5 nerve is involved in a lower back pain?
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L5
Motor: Big toe dorsiflexion (extensor hallucis longus), foot eversion Reflex: None Sensory: Dorsum of the foot and lateral aspect (peroneus muscles). of the lower leg. |
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what would be the motor, sensory and reflex deficit if S1 nerve is involved in a lower back pain?
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S1
Motor: Plantar flexion (gastrocnemius/soleus), gluteus maximus Reflex: Achilles Sensory: Plantar and lateral aspects of the foot. (hip extension). |
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what is fibromyalgia?
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>>A connective tissue disorder characterized by myalgias, weakness, and fatigability.
>>Inflammation is notably absent |
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Hx/PE of fibromyalgia?
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>>women 30–50 years of age; >>associated with depression,
anxiety, sleep disorders, and IBS. |
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Dx of fibromyalgia?
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Multiple (≥ 11 of 18), diffuse tender points are seen
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what if there is <11 tender points or or non-fibromyalgia-associated
tender points, what is the diagnosis? |
myofascial pain syndrome
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Rx of fibromyalgia
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ANTIDEPRESSANT, stretching, heat application, hydrotherapy, transcutaneous
electrical nerve stimulation (TENS). |
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what are the causes of hyperurecemia?
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>>↑ cell turnover (hemolysis, blast crisis, tumor lysis)
>>Cyclosporine >>Diabetes insipidus >>Diet (e.g., ↑ red meat, alcohol) >>Diuretics >>Lead poisoning >>Lesch-Nyhan syndrome >>Salicylates |
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what is the most effective medication for gout during a flare?
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COLCHICINE, inhibits chemotaxis and is most effective when used early, during a gout flare.
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Hx/PE of gout
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>>excruciating joint pain of sudden onset that awakens the patient from sleep.
>>affects the first MTP joint (podagra) and the midfoot, others are spared. >>Tophi (urate crystals deposits → deformed joints) maybe seen in chronic disease |
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what is gout?
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acute monoarticular arthritis resulting from intra-articular
deposition of monosodium urate crystals. >>most common in the male gender |
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In gout, what would be shown in the aspirate?
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>>needle-shaped
>>negatively birefringent crystals >>Elevated WBC count during flares >>uric acid may or may not be up |
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gout: what would be seen on an x-ray?
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>>x-ray: Punched-out erosions with overhanging cortical bone (“rat-bite” erosions)
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treatment of gout: acute attacks
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Acute attacks: High-dose NSAIDs (e.g., indomethacin), colchicine, and/or steroids.
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treatment of gout: maintenance therapy
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>>Weight loss and avoidance of triggers of hyperuricemia will prevent recurrent
attacks in many patients. >>Maintenance therapy: Allopurinol for overproducers and refractory cases; probenecid for undersecretors. |
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gout and pseudogout:
shape and crystal bifringence: |
Gout: Needle shaped with negative bifingence
Pseudogout: Rhomboid shaped with positive bifingence. |
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what is osteoarthritis?
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>>chronic, noninflammatory arthritis of movable joints (e.g., DIP joints).
>>deterioration of the articular cartilage and osteophyte formation at joint surfaces. |
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risk factors of osteroarthritis?
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family history, obesity, and a history of joint trauma.
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Hx/PE: of osteoarthritis
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>>Crepitus
>>pain that worsens with activity and weight bearing but improves with rest. >>decrease ROM |
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Dx of osteoarthritis
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>>Radiographs show joint space narrowing, osteophytes, subchondral sclerosis, and subchondral bone cysts.
>>Synovial fluid shows straw-colored fluid, normal viscosity, and a WBC count < 3000 cells/μL. |
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Rx: osteoarthritis:
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>>Physical therapy, weight reduction, NSAIDs.
>>Intra-articular corticosteroid injections may provide temporary relief. >>Consider joint replacement (e.g., total hip/knee arthroplasty) in advanced cases. |
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polymyositis vs. dermatomyosistis
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>>Polymyositis is a progressive, systemic connective tissue disease characterized by striated muscle inflammation.
>>Dermatomyositis presents with symptoms of polymyositis plus cutaneous involvement |
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risk factors for polymyositis and dermatomyositis
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>>patients 50–70 years of age >>the male-to-female ratio is
1:2. >>African-Americans are affected more often than Caucasians |
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how does polymyositis presents?
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Presents with symmetric, progressive proximal muscle
weakness; pain; and difficulty breathing or swallowing (advanced disease). |
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how does dermatomyositis presents?
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>>Patients may have heliotrope rash (a violaceous periorbital rash),
>>“shawl sign” (a rash involving the shoulders, upper chest, and back), >>Gottron’s papules (a papular rash with scales located on the dorsa of the hands, over bony prominences). |
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what are polymyositis and dermatomyositis increase risk of?
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>>myocarditis
>>cardiac conduction deficits >>malignancy |
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Dx: of polymyositis and dermatomyositis
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>>↑ serum CK, aldolase, and CPK.
>>EMG shows fibrillations. >>Muscle biopsy reveals inflammation and muscle fibers in varying stages of necrosis and regeneration. |
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Tx: polymyositis and dermatomyositis
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>>High-dose corticosteroids with taper after 4–6 weeks to ↓ the maintenance
dose. >>Azathioprine and/or methotrexate can be used as an adjunct. |
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what is rheumatoid arthritis?
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Systemic inflammatory disease of symmetric
involvement of both large and small joints that → synovial hypertrophy and pannus formation → erosion of adjacent cartilage, bone, and tendons |
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RF or rheumatoid arthritis (3)?
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>>female gender
>>age 35–50 >>HLA-DR4. |
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presentation of RA
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>>Insidious onset of morning stiffness for > 1 hour w/ pain of the MCP and PIP joints for > 6 weeks.
>>Ulnar deviation of the fingers is seen with MCP joint hypertrophy >>may also present swan-neck and boutonnière deformities), Baker’s cysts, vasculitis, atlantoaxial subluxation, carpal tunnel syndrome, and Felty’s syndrome. |
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what is felty's syndrome
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RA + neutropenia and splenomegally
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what would one see in the labs of RA? RF, ESR, synovial fluid, WBC count.
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Labs:
■ ↑ RF (anti-Fc IgG antibody) in > 75% of cases. ■ ↑ ESR may also be seen. ■ Synovial fluid aspirate shows turbid fluid, ↓ viscosity, and an ↑ WBC count (3000–50,000 cells/μL). |
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what would one see in the radiography of RA?
early and late |
>>Early: Soft tissue swelling and juxta-articular demineralization.
>>Late: Joint space narrowing and erosions. |
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Tx of RA
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NSAIDs.
■ (DMARDs) should be started early. First-line: methotrexate, hydroxychloroquine, and TNF inhibitors. Second-line: penicillamine and cyclosporine. |
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describe JRA
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A nonmigratory, non-suppurative mono- and polyarthropathy with bony destruction that occurs in patients ≤ 16 years of age and lasts > 6 weeks
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what are its 3 types?
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>>puciarticular
>>polyarticular >>acute febrile |
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pauciarticular
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>>fever, nodules, erythematous rashes, pericarditis, and fatigue.
>>An asymmetric arthritis that involves weight-bearing joints. Associated with an ↑ risk of iridocyclitis that → blindness if left untreated. |
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Polyarticular
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Resembles RA with symmetric involvement of multiple (≥ 5) small joints. Systemic features are less prominent; carries a ↓ risk
of iridocyclitis. |
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acute febrile
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>>manifests as arthritis with
daily high, spiking fevers and an evanescent, salmon-colored rash. >>Hepatosplenomegaly and serositis may also be seen. >>No iridocyclitis is present; >>remission occurs within one year. |
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how is JRA diagnosed?
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There is no diagnostic test for JRA.
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what would one see in the labs of JRA?
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Labs:
■ RF in 15% of cases. ■ ANA may be , especially in the pauciarticular subtype. ■ ↑ ESR, WBC count, and platelets. |
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what would one see in the imaging of JRA?
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Soft tissue swelling and osteoporosis may be seen
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treatment of JRA?
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>>NSAIDs or corticosteroids; >>methotrexate is second-line therapy.
>>ROM and strengthening exercises |
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what is scleroderma?
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>>excessive deposition of collagen.
>>Commonly manifests as CREST syndrome but can also occur in a diffuse form. >>RF: female gender and age 35–50. |
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hX/PE: of scleroderma
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>>symmetric thickening of the skin
>>CREST syndrome involves Calcinosis, Raynaud’s phenomenon, Esophageal dysmotility, Sclerodactyly, and Telangiectasias. >>The diffuse form can → PULMONARY FIBROSIS, cor pulmonale, acute renal failure, and malignant hypertension |
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labs of scleroderma:
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RF and ANA may be + .
■ Anticentromere antibodies are specific for CREST syndrome. ■ Anti-Scl-70 (antitopoisomerase 1) antibodies: a poor prognosis. ■ Eosinophilia may be seen. |
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tx of scleroderma:
>>acute flares >>skin changes >>raynaud's >>renal disease and malignant HTN |
Steroids for acute flares; penicillamine can be used for skin changes.
■ Calcium channel blockers for Raynaud’s. ■ ACEIs for renal disease and malignant hypertension. |
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SLE:
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A multisystem autoimmune disorder related to antibody-mediated cellular attack
and deposition of antigen-antibody complexes. |
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RF of SLE
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AA women
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Hx/PE of SLE
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"DOPAMIN RASH" >5
discoid rash, oral ulcers, photosensitivity, arthritis, malar rash, immunologic (anti-dsDNA, anti-smith, anti-cardiolipin ab), neurologic (psychosi), renal failure (MCC of death),ANA +, serositis and hemolytic anemia |
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SLE diagnosis most sensitive screening test
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ANA is highly sensitive.
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SLE: most specific
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■ Anti-dsDNA and anti-Sm antibodies are highly specific but not as sensitive.
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SLE: drug induced
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■ Drug-induced SLE: antihistone antibodies are seen in 100% of cases
but are nonspecific. |
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SLE: neonatal
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■ Neonatal SLE: anti-Ro antibodies.
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SLE: what else can also be seen
|
■ The following may also be seen:
■ Antiphospholipid antibodies. ■ Anemia, leukopenia, and/or thrombocytopenia. ■ Proteinuria and/or casts. |
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Tx: mild joint symptoms of SLE
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Treat with NSAIDs for mild joint symptoms.
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Tx: acute exacerbation of SLE
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■ Steroids for acute exacerbations.
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Tx: of progressive or refractory cases of SLE
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■ Steroids, hydroxychloroquine, cyclophosphamide, and azathioprine for progressive or refractory cases
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most feared complication of temporal arteritis
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blindness 2° to occlusion of the central retinal artery (a branch of the internal carotid artery).
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what is temporal arteritis?
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giant cell arteritis: subacute granulomatous inflammation of the large vessels, including the aorta, external carotid (especially the temporal
branch), and vertebral arteries. |
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RF of temporal arteritis?
|
>>polymyalgia rheumatica
>>age > 50 >>female gender. |
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Hx/PE: temporal arteritis?
|
>>New headache (unilateral or bilateral); scalp pain and temporal tenderness; jaw claudication.
■ Fever; transient or permanent monocular >>BLINDNESS; weight loss; myalgias/ arthralgias (especially of the shoulders and hips). |
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Dx: temporal arteritis?
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ESR > 50 (usually > 100).
■ Ophthalmologic evaluation. ■ Temporal artery biopsy: Look for thrombosis; necrosis of the media; and lymphocytes, plasma cells, and giant cells. |
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treatment of temporal arteritis?
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>>High-dose prednisone for 1–2 months before tapering.
>>Obtain a biopsy, but do not delay treatment >>follow-up eye exam. |
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PMR: RF
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RF: female gender and age > 50.
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PMR: Hx/PE
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Hx/PE:
>> Pain and stiffness of the shoulder and pelvic girdle areas with difficulty getting out of a chair or lifting the arms above the head. >>Other symptoms include fever |
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PMR: Dx
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Markedly ↑ ESR, often associated with anemia.
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PMR: Rx
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Low-dose prednisone (10–20 mg/day).
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what is developmental dysplasia of the hip?
|
>>congenital hip dislocation; can result in subluxed, dislocatable, or dislocated femoral heads
>>poor development of acetebelum due to excessive uterine packing in the flexed and adducted position (e.g., breech presentation) → excessive stretching of the posterior hip capsule and adductor muscle contracture. |
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presentaion of DDH:
|
first-born females born in the breech position.
Barlow’s maneuver Ortolani’s maneuver Allis’ (Galeazzi’s) sign Asymmetric skin folds |
|
Barlow’s maneuver
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Pressure is placed on the inner aspect of the abducted thigh, and the hip is then adducted → posterior dislocation.
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Ortolani’s maneuver
|
The thighs are gently abducted from the midline with anterior pressure on the greater trochanter. A soft click signifies reduction
of the femoral head into the acetabulum. |
|
Allis’ (Galeazzi’s) sign
|
The knees are at unequal heights when the hips and knees are flexed (the dislocated side is lower).
|
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Dx: of DDH
|
EARLY DETECTION IS CRIITICAL to allow for proper hip development.
>>Ultrasound may be helpful, especially after 10 weeks of age. |
|
Treatment of DDH at ff.
<6 months 6-15 months 15–24 months |
Begin treatment early.
■ < 6 months: Splint with a Pavlik harness (maintains hip flexed and abducted). ■ 6–15 months: Spica cast. ■ 15–24 months: Open reduction. |
|
complications of DDH
|
>>Joint contractures and AVN of the femoral head.
>>Without treatment, a significant defect patients < 2 years of age. |
|
what are the DDx of a limp:
|
"STARTSS HOTT"
Septic joint Tumor Avascular necrosis (Legg-Calvé-Perthes) Rheumatoid arthritis/JRA Tuberculosis Sickle cell disease SCFE Henoch-Schönlein purpura Osteomyelitis Trauma Toxic synovitis |
|
what is Legg-Calvé-Perthes Disease?
|
>>AVN of the femoral head of unknown etiology
>>Most commonly found in boys 4–10 years of age. >>self-limited disease, with symptoms lasting < 18 months. |
|
Legg-Calvé-Perthes Disease Hx/PE?
|
>>asymptomatic at first, but patients can develop a painless limp.
>>If pain is present, it can be referred to the knee. >>Limited abduction and internal rotation; >>atrophy of the affected leg. >> Usually unilateral |
|
Tx:Legg-Calvé-Perthes disease. when ithere is limited femoral head involvement or if full ROM is present.
|
Observation
|
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Tx:Legg-Calvé-Perthes disease. when extensive or if there is ↓ ROM
|
consider bracing, hip abduction with a Petrie cast, or an osteotomy.
|
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what is the good prognosis of Legg-Calvé-Perthes disease?
|
>>if the patient is < 5 years of age
>has full ROM >>↓ femoral head involvement, and a stable joint. |
|
what is Slipped Capital Femoral Epiphysis (SCFE)
|
Separation of the proximal femoral epiphysis through the growth plate → medial
and posterior displacement of the femoral head. |
|
what is posterior displacement of the femoral head in SCFE due to?
|
due to an imbalance between growth hormone and sex hormones.
|
|
RF of SCFE
|
obesity
age 11–13 male gender AA |
|
what is SCFE associated with?
|
hypothyroidism and other endocrinopathies.
|
|
Hx/PE: Slipped Capital Femoral Epiphysis (SCFE)
|
>>acute or insidious thigh or knee pain and a painful limp
>>in acute cases inability to bear weight. >>Bilateral 30% >>Limited internal rotation and abduction of the hip. |
|
Dx: of SCFE
|
>>Radiographs of both hips in AP and frog-leg lateral views reveal posterior and medial displacement of the femoral head
>>Rule out hypothyroidism with TSH. |
|
Tx: of SCFE
|
>> progressive, so treatment should begin promptly
>>No weight bearing should be allowed until the defect is surgically stabilized. >>Gentle closed reduction only in acute slips |
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complications of SCFE (3)
|
>>Chondrolysis
>>AVN of the femoral head >>premature hip osteoarthritis → hip arthroplasty. |
|
osteosarcoma
|
usually occurs at the >>metaphyseal regions of the distal femur, proximal tibia, and proximal humerus
>>often metastasizes to the lung |
|
osteosarcoma risk factors
|
male gender and age 20–30.
|
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osteosarcoma: Hx/PE
|
>>progressive then intractable PAIN THAT IS WORSE AT NIGHT.
>>fever, weight loss, and night sweats may >>Erythema and enlargement over the site of the tumor maybe seen be present. |
|
Dx: osteosarcoma
|
>>CODMAN'S TRIANGLE (periosteal new bone formation at the diaphyseal end of the lesion)
>>SUNBURST PATTERN >>ONION SKINNING (classic for ewing sarcoma) |
|
once osteosarcoma is diaganosed what is the next best step of management?
|
MRI and CT for staging (soft tissue and bony invasion) and to plan for surgery.
|
|
Tx osteosarcoma
|
>>Limb-sparing surgical procedures and pre- and postoperative chemotherapy
(e.g., methotrexate, doxorubicin, cisplatin, ifosfamide). >> Amputation may be necessary |
|
Common Adult Orthopedic Injuries: Humerus fracture
|
Direct trauma. May have radial nerve palsy → wrist drop and loss of thumb abduction
|
|
Common Adult Orthopedic Injuries :Humerus fracture
|
Hanging-arm cast vs. coaptation splint and sling.
|
|
Common Adult Orthopedic Injuries: “Nightstick fracture”
|
Ulnar shaft fracture resulting from self-defense with the arm against a blunt object.
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Common Adult Orthopedic Injuries: “Nightstick fracture” treatment
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Open reduction and internal fixation (ORIF) if significantly displaced.
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Common Adult Orthopedic Injuries: Monteggia’s fracture
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Diaphyseal fracture of the proximal ulna with subluxation of the radial head
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Common Adult Orthopedic Injuries: Monteggia’s fracture treatment
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ORIF of the shaft fracture (due to poor fracture diaphyseal blood supply) and closed reduction
of the radial head. |
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Common Adult Orthopedic Injuries:Galeazzi’s fracture
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Diaphyseal fracture of the radius with dislocation of the distal radioulnar joint. Results from a direct blow to the radius. radioulnar joint.
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Common Adult Orthopedic Injuries: Galeazzi’s fracture treatment
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ORIF of the radius and casting of the forearm in supination to reduce the distal fracture.
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Common Adult Orthopedic Injuries: Tibial fracture
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Direct trauma. Watch for compartment syndrome.
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Common Adult Orthopedic Injuries:Tibial fracture treatment
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Casting vs. intramedullary nailing.
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Common Adult Orthopedic Injuries: Hip fracture
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↑ risk with osteoporosis. Presents with a shortened and externally rotated leg.may Displaced femoral neck fractures: Associated with an ↑ risk of AVN, nonunion, and DVTs.
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Common Adult Orthopedic Injuries: Hip fracture treatment
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>>ORIF with parallel pinning of the femoral neck.
>>Displaced fractures in elderly patients require a hip hemiarthroplasty. >>Anticoagulate to ↓ the likelihood of DVTs. |
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Common Adult Orthopedic Injuries: Femoral fracture
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Direct trauma. Beware of fat emboli, which present with fever, change in mental status, dyspnea, hypoxia, petechiae, and ↓ platelets.
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Common Adult Orthopedic Injuries: Femoral fracture treatment
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Intramedullary nailing of the femur. Irrigate and debride open fractures.
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Common Adult Orthopedic Injuries: Open fractures
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An orthopedic emergency; patients must be taken to the OR in < 6 hours owing to ↑ infection risk.
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Common Adult Orthopedic Injuries:Open fractures treatment
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OR emergently to repair fracture. Treat with antibiotics.
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Common Adult Orthopedic Injuries: Achilles tendon rupture
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Presents with a sudden “pop” like a rifle shot. More likely with ↓ physical conditioning.
Exam shows limited plantar flexion and a Thompson’s test (pressure on the gastrocnemius → absent foot plantar flexion). |
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Common Adult Orthopedic Injuries: Achilles tendon rupture treatment
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Treat surgically followed by long leg cast for six weeks.
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Common Adult Orthopedic Injuries: Knee injuries (3 types)
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ACL
PCL meniscal tears |
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Common Adult Orthopedic Injuries: Knee injury ACL
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Present with knee instability, edema, and hematoma.
ACL: ■ Results from forced hyperflexion or impact to an extended knee. tendons. ■ positive anterior drawer and Lachman’s tests. ■ Rule out a meniscal or MCL injury. |
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Common Adult Orthopedic Injuries: Knee injury ACL treatment
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Treatment of ACL injuries is generally surgical with graft from the patellar or hamstring an extended knee. tendons.
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Common Adult Orthopedic Injuries: Knee injury PCL
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PCL:
■ Results from forced hyperextension. ■ posterior drawer test. |
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Common Adult Orthopedic Injuries: Knee injury PCL treatment
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Operative PCL repair is reserved for highly competitive athletes
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Common Adult Orthopedic Injuries: Knee injury medial meniscus
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■ Clicking or locking may be present.
■ Exam shows joint line tenderness and a McMurray’s test. |
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Common Adult Orthopedic Injuries: Knee injury medial meniscus/LCL
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Treatment of MCL/LCL and meniscal tears is usually conservative.
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