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180 Cards in this Set

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Name all 8 Common Adult Orthopedic Injuries:
shoulder dislocation, hip dislocation, colle's fracture, boxer's fracture, humerus fracture, "Night stick" fracture, monteggia's fracture
Common Adult Orthopedic Injuries: what are the two types of Shoulder dislocation?
Anterior Shoulder dislocation and posterior dislocation
what is the most common shoulder dislocation?
anterior dislocation
Common Adult Orthopedic Injuries: Anterior shoulder dislocation presentation and what nerve and artery are involved?
the axilliary nerve and artery are involved. Patient comes in holding the arm slightly abducted and externally rotated.
Common Adult Orthopedic Injuries: Shoulder dislocation Tx. acute and recurrent dislocations
reduction followed by a sling swath. Recurrent dislocations may need surgical repair
Common Adult Orthopedic Injuries: Posterior dislocation of the shoulder is associated with what?
seizure and electrocution
Common Adult Orthopedic Injuries: Posterior shoulder dislocation injury: what artery and describe the presentation
will injure the radial artery. Patients hold the arm in an adduction and internal rotation.
Common Adult Orthopedic Injuries: 2 type of Hip dislocations
anterior and posterior hip dislocations
Common Adult Orthopedic Injuries: anterior hip dislocation can injure what nerve
obturator nerve
What is the most common hip dislocation?
posterior hip dislocation
Common Adult Orthopedic Injuries: Posterior hip dislocations is associated with what?
sciatic nerve injury and avascular necrosis
Common Adult Orthopedic Injuries: Posterior hip dislocations are common cause of what?
It occurs via a "dash board injury". a posteriorly direct force on an internally rotated, flexed, adducted hip.
Common Adult Orthopedic Injuries: Posterior hip dislocations Tx:
closed reduction followed by abduction pillow/bracing. Evaluated with CT scan after reduction
Common Adult Orthopedic Injuries: Colle's fracture association.
commonly seen in the elderly (osteoporosis) and children
Common Adult Orthopedic Injuries: Colle's fracture presentation
It involves the distal radius. Often results from a fall onto an outstreched hand, leading to a dorsally displaced, dorsally angulated fracture
Common adult orthopedic Injuries: Colle's fracture Tx:
closed reduction followed by a long arm cast; open reduction if fracture is intrarticular.
Common adult orthopedic Injuries: what is the most commonly injured carpal bone?
scaphoid fracture
Common adult orthopedic Injuries: how is Scaphoid fracture diagnosed?
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.
Common adult orthopedic Injuries: Scaphoid fracture Tx:
thumb spica cast. If displacement or navicular or non-union is present do an open reduction.
Common adult orthopedic Injuries: proximal third scaphoid bone fracture complication.
AVN may result to disruption of blood flow
Common adult orthopedic Injuries: Boxer's fracture presentation
fracture of the fifth metacarpal neck due to a forward trauma of a closed fist (ie. punching a wall)
Common adult orthopedic Injuries: Boxer's fracture Tx:
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)
what are the 6P's of compartment syndrome
Pain
Pallor
Paresthesias
Poikilothermia
Paralysis
Pulselessness
complications of supracondylar fractures due to compartment syndrome
Volkmann’s contracture of the
wrist and fingers.
what is compartment syndrome
↑ pressure within a confined space that compromises nerve, muscle, and soft tissue perfusion.
where is the most common location of compartment syndrome
anterior compartment of the
lower leg and forearm.
presentation of compartment syndrome
pain with passive motion
of the fingers and toes; paresthesias, pallor, poikilothermia, pulselessness,
and paralysis.
how is compartment syndrome diagnosed?
Measure compartment pressures (usually ≥ 30 mmHg); measure delta
pressures (diastolic pressure − compartment pressure).
treatment for compartment syndrome?
Immediate fasciotomy to ↓ pressures and ↑ tissue perfusion.
Risk factors for malignancy in lower back pain (6)
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.
contraindicated in lower back pain
Prolonged bed rest is contraindicated
causes of herniated disk
degenerative changes, trauma, or neck/back strain or sprain
Most common area of herniated disk
lumbar region, especially at L4–L5 and L5–S1.
Dx and treatment: Bowel or bladder dysfunction, impotence, and saddle-area anesthesia
cauda equina syndrome,
which is a surgical emergency
Hx and PE of herniated disk
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.
what should be ordered is other lower back pain is suspected (ie. infection)
plain radiograph if other causes of back pain are suspected
what should be ordered if after conservative management of lower back pain, it would not resolve?
MRI if symptoms are refractory to conservative management
lower back pain treatment
NSAIDs, physical therapy, and local heat → resolution within four weeks
Tx: lower back pain with neurological symptom such a cauda equina.
indications for discectomy.
what is spinal stenosis?
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.
spinal stenosis Hx/PE
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
how is spinal stenosis diaganosed?
Radiographs show degenerative changes and a narrowed spinal canal.
■ MRI or CT shows spinal stenosis.
Treatment of spinal stenosis:
mild to moderate
Mild to moderate: NSAIDs and abdominal muscle strengthening.
treatment of lumbar spinal stenosis: Advanced stage
■ Advanced: Epidural steroid injections can provide relief.
treatment of lumbar spinal stenosis: refractory stage
■ Refractory: Surgical laminectomy may achieve significant short-term success,
but many patients will have a recurrence of symptoms
what is ankylosing spondylitis?
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.
ankylosing spondylitis Hx/PE?
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.
ankylosing spondylitis Hx/PE II?
↓ 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.
what other diagnosis must be rule out in ankylosing spondylitis?
Other seronegative spondyloarthropathies must be ruled out such as Reactive arthritis (aka Reiter’s syndrome) and Psoriatic arthritis
Reiter’s syndrome
disease of young men
arthritis, uveitis, conjunctivitis, and urethritis usually
follow an infection with Campylobacter, Shigella, Salmonella, Chlamydia,
or Ureaplasma
Psoriatic arthritis
An oligoarthritis of the DIP joints. Associated with psoriatic skin changes and sausage-shaped digits.
how is ankylosing spondylitis diagnosed
 + HLA-B27.
Radiographs show bamboo spine and fused sacroiliac joints.
■ ESR ↑.
■  - RF;  - ANA
treatment for ankylosing spondylitis: for pain, for improvement of posture and refractory cases
NSAIDs (e.g., indomethacin) for pain; exercise to improve posture and breathing.
■ Tumor necrosis factor (TNF) inhibitors are used in refractory cases.
what is duchenne Muscular dystrophy and onset
X-linked recessive disorder resulting from a deficiency of dystrophin, a cytoskeletal protein.
Onset is usually at 3–5 years of age.
Hx/PE: duchenne muscular dystrophy
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.
Dx of duchenne muscular dystrophy
 (-) dystrophin immunostain
↑ CK.
■ EMG shows polyphasic potentials and ↑ recruitment.
Dystrophin mutation is sometimes seen.
■ Muscle biopsy
treatment of duchenne muscular dystrophy
Physical therapy
Perform Achilles tendon release if necessary.
what would be the motor, sensory and reflex deficit if the nerve L4 is affected on a lower back pain?
L4:
Motor: Foot dorsiflexion (tibialis anterior).
reflex: Patellar
sensory: Medial aspect of the lower leg.
what would be the motor, sensory and reflex deficiency if L5 nerve is involved in a lower back pain?
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.
what would be the motor, sensory and reflex deficit if S1 nerve is involved in a lower back pain?
S1
Motor: Plantar flexion (gastrocnemius/soleus), gluteus maximus
Reflex: Achilles
Sensory: Plantar and lateral aspects of the foot. (hip extension).
what is fibromyalgia?
>>A connective tissue disorder characterized by myalgias, weakness, and fatigability.
>>Inflammation is notably absent
Hx/PE of fibromyalgia?
>>women 30–50 years of age; >>associated with depression,
anxiety, sleep disorders, and IBS.
Dx of fibromyalgia?
Multiple (≥ 11 of 18), diffuse tender points are seen
what if there is <11 tender points or or non-fibromyalgia-associated
tender points, what is the diagnosis?
myofascial pain syndrome
Rx of fibromyalgia
ANTIDEPRESSANT, stretching, heat application, hydrotherapy, transcutaneous
electrical nerve stimulation (TENS).
what are the causes of hyperurecemia?
>>↑ cell turnover (hemolysis, blast crisis, tumor lysis)
>>Cyclosporine
>>Diabetes insipidus
>>Diet (e.g., ↑ red meat,
alcohol)
>>Diuretics
>>Lead poisoning
>>Lesch-Nyhan syndrome
>>Salicylates
what is the most effective medication for gout during a flare?
COLCHICINE, inhibits chemotaxis and is most effective when used early, during a gout flare.
Hx/PE of gout
>>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
what is gout?
acute monoarticular arthritis resulting from intra-articular
deposition of monosodium urate crystals.
>>most common in the male gender
In gout, what would be shown in the aspirate?
>>needle-shaped
>>negatively birefringent crystals
>>Elevated WBC count during flares
>>uric acid may or may not be up
gout: what would be seen on an x-ray?
>>x-ray: Punched-out erosions with overhanging cortical bone (“rat-bite” erosions)
treatment of gout: acute attacks
Acute attacks: High-dose NSAIDs (e.g., indomethacin), colchicine, and/or steroids.
treatment of gout: maintenance therapy
>>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.
gout and pseudogout:
shape and crystal bifringence:
Gout: Needle shaped with negative bifingence
Pseudogout: Rhomboid shaped with positive bifingence.
what is osteoarthritis?
>>chronic, noninflammatory arthritis of movable joints (e.g., DIP joints).
>>deterioration of the articular cartilage and osteophyte
formation at joint surfaces.
risk factors of osteroarthritis?
family history, obesity, and a history of joint trauma.
Hx/PE: of osteoarthritis
>>Crepitus
>>pain that worsens with activity
and weight bearing but improves with rest.
>>decrease ROM
Dx of osteoarthritis
>>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.
Rx: osteoarthritis:
>>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.
polymyositis vs. dermatomyosistis
>>Polymyositis is a progressive, systemic connective tissue disease characterized by striated muscle inflammation.
>>Dermatomyositis presents with symptoms of polymyositis plus cutaneous involvement
risk factors for polymyositis and dermatomyositis
>>patients 50–70 years of age >>the male-to-female ratio is
1:2.
>>African-Americans are affected more often than Caucasians
how does polymyositis presents?
Presents with symmetric, progressive proximal muscle
weakness; pain; and difficulty breathing or swallowing (advanced disease).
how does dermatomyositis presents?
>>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).
what are polymyositis and dermatomyositis increase risk of?
>>myocarditis
>>cardiac conduction deficits
>>malignancy
Dx: of polymyositis and dermatomyositis
>>↑ serum CK, aldolase, and CPK.
>>EMG shows fibrillations.
>>Muscle biopsy reveals inflammation and muscle fibers in varying stages of
necrosis and regeneration.
Tx: polymyositis and dermatomyositis
>>High-dose corticosteroids with taper after 4–6 weeks to ↓ the maintenance
dose.
>>Azathioprine and/or methotrexate can be used as an adjunct.
what is rheumatoid arthritis?
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
RF or rheumatoid arthritis (3)?
>>female gender
>>age 35–50
>>HLA-DR4.
presentation of RA
>>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.
what is felty's syndrome
RA + neutropenia and splenomegally
what would one see in the labs of RA? RF, ESR, synovial fluid, WBC count.
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).
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.
Tx of RA
NSAIDs.
■ (DMARDs) should be started
early.
First-line: methotrexate, hydroxychloroquine, and TNF inhibitors.
Second-line: penicillamine and cyclosporine.
describe JRA
A nonmigratory, non-suppurative mono- and polyarthropathy with bony destruction that occurs in patients ≤ 16 years of age and lasts > 6 weeks
what are its 3 types?
>>puciarticular
>>polyarticular
>>acute febrile
pauciarticular
>>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.
Polyarticular
Resembles RA with symmetric involvement of multiple (≥ 5) small joints. Systemic features are less prominent; carries a ↓ risk
of iridocyclitis.
acute febrile
>>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.
how is JRA diagnosed?
There is no diagnostic test for JRA.
what would one see in the labs of JRA?
Labs:
■  RF in 15% of cases.
■ ANA may be , especially in the pauciarticular subtype.
■ ↑ ESR, WBC count, and platelets.
what would one see in the imaging of JRA?
Soft tissue swelling and osteoporosis may be seen
treatment of JRA?
>>NSAIDs or corticosteroids; >>methotrexate is second-line therapy.
>>ROM and strengthening exercises
what is scleroderma?
>>excessive deposition of collagen.
>>Commonly manifests as CREST syndrome but can also occur in a diffuse form.
>>RF: female gender and age 35–50.
hX/PE: of scleroderma
>>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
labs of scleroderma:
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.
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.
SLE:
A multisystem autoimmune disorder related to antibody-mediated cellular attack
and deposition of antigen-antibody complexes.
RF of SLE
AA women
Hx/PE of SLE
"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
SLE diagnosis most sensitive screening test
ANA is highly sensitive.
SLE: most specific
■ Anti-dsDNA and anti-Sm antibodies are highly specific but not as sensitive.
SLE: drug induced
■ Drug-induced SLE:  antihistone antibodies are seen in 100% of cases
but are nonspecific.
SLE: neonatal
■ Neonatal SLE:  anti-Ro antibodies.
SLE: what else can also be seen
■ The following may also be seen:
■ Antiphospholipid antibodies.
■ Anemia, leukopenia, and/or thrombocytopenia.
■ Proteinuria and/or casts.
Tx: mild joint symptoms of SLE
Treat with NSAIDs for mild joint symptoms.
Tx: acute exacerbation of SLE
■ Steroids for acute exacerbations.
Tx: of progressive or refractory cases of SLE
■ Steroids, hydroxychloroquine, cyclophosphamide, and azathioprine for progressive or refractory cases
most feared complication of temporal arteritis
blindness 2° to occlusion of the central retinal artery (a branch of the internal carotid artery).
what is temporal arteritis?
giant cell arteritis: subacute granulomatous inflammation of the large vessels, including the aorta, external carotid (especially the temporal
branch), and vertebral arteries.
RF of temporal arteritis?
>>polymyalgia rheumatica
>>age > 50
>>female gender.
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).
Dx: temporal arteritis?
ESR > 50 (usually > 100).
■ Ophthalmologic evaluation.
■ Temporal artery biopsy: Look for thrombosis; necrosis of the media; and lymphocytes, plasma cells, and giant cells.
treatment of temporal arteritis?
>>High-dose prednisone for 1–2 months before tapering.
>>Obtain a biopsy, but do not delay treatment
>>follow-up eye exam.
PMR: RF
RF: female gender and age > 50.
PMR: Hx/PE
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
PMR: Dx
Markedly ↑ ESR, often associated with anemia.
PMR: Rx
Low-dose prednisone (10–20 mg/day).
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.
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
Pressure is placed on the inner aspect of the abducted thigh, and the hip is then adducted → posterior dislocation.
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).
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
Tx:Legg-Calvé-Perthes disease. when extensive or if there is ↓ ROM
consider bracing, hip abduction with a Petrie cast, or an osteotomy.
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
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.
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.
Common Adult Orthopedic Injuries: “Nightstick fracture” treatment
Open reduction and internal fixation (ORIF) if significantly displaced.
Common Adult Orthopedic Injuries: Monteggia’s fracture
Diaphyseal fracture of the proximal ulna with subluxation of the radial head
Common Adult Orthopedic Injuries: Monteggia’s fracture treatment
ORIF of the shaft fracture (due to poor fracture diaphyseal blood supply) and closed reduction
of the radial head.
Common Adult Orthopedic Injuries:Galeazzi’s fracture
Diaphyseal fracture of the radius with dislocation of the distal radioulnar joint. Results from a direct blow to the radius. radioulnar joint.
Common Adult Orthopedic Injuries: Galeazzi’s fracture treatment
ORIF of the radius and casting of the forearm in supination to reduce the distal fracture.
Common Adult Orthopedic Injuries: Tibial fracture
Direct trauma. Watch for compartment syndrome.
Common Adult Orthopedic Injuries:Tibial fracture treatment
Casting vs. intramedullary nailing.
Common Adult Orthopedic Injuries: Hip fracture
↑ 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.
Common Adult Orthopedic Injuries: Hip fracture treatment
>>ORIF with parallel pinning of the femoral neck.
>>Displaced fractures in elderly patients require a hip hemiarthroplasty.
>>Anticoagulate to ↓ the likelihood of DVTs.
Common Adult Orthopedic Injuries: Femoral fracture
Direct trauma. Beware of fat emboli, which present with fever, change in mental status, dyspnea, hypoxia, petechiae, and ↓ platelets.
Common Adult Orthopedic Injuries: Femoral fracture treatment
Intramedullary nailing of the femur. Irrigate and debride open fractures.
Common Adult Orthopedic Injuries: Open fractures
An orthopedic emergency; patients must be taken to the OR in < 6 hours owing to ↑ infection risk.
Common Adult Orthopedic Injuries:Open fractures treatment
OR emergently to repair fracture. Treat with antibiotics.
Common Adult Orthopedic Injuries: Achilles tendon rupture
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).
Common Adult Orthopedic Injuries: Achilles tendon rupture treatment
Treat surgically followed by long leg cast for six weeks.
Common Adult Orthopedic Injuries: Knee injuries (3 types)
ACL
PCL
meniscal tears
Common Adult Orthopedic Injuries: Knee injury ACL
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.
Common Adult Orthopedic Injuries: Knee injury ACL treatment
Treatment of ACL injuries is generally surgical with graft from the patellar or hamstring an extended knee. tendons.
Common Adult Orthopedic Injuries: Knee injury PCL
PCL:
■ Results from forced hyperextension.
■  posterior drawer test.
Common Adult Orthopedic Injuries: Knee injury PCL treatment
Operative PCL repair is reserved for highly competitive athletes
Common Adult Orthopedic Injuries: Knee injury medial meniscus
■ Clicking or locking may be present.
■ Exam shows joint line tenderness and a 
McMurray’s test.
Common Adult Orthopedic Injuries: Knee injury medial meniscus/LCL
Treatment of MCL/LCL and meniscal tears is usually conservative.