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144 Cards in this Set

  • Front
  • Back
The injury called the "unholy triad"
damage to:
- MCL
- medial meniscus
- ACL
Positive anterior drawer sign indicates...
torn ACL
abnormal passive abduction indicates...
torn MCL
Shoulder muscles that form rotator cuff and their functions
Supraspinatus - ABducts arm (helps deltoid)
Infraspinatus - laterally rotates arm
Teres minor - adducts and laterally rotates arm
Subscapularis - medially rotates and adducts arm
Common injury: upper trunk
lesioned by trauma
common injury: C7 root
compressed by cervical disc lesion
common injuries (3): axillary nerve
lesioned by
- fracture of surgical neck of humerus
- dislocation of humerus
- intramuscular injections
common injuries (2): lower trunk of brachial plexus
compressed by cervical rib
or by Pancoast tumor of lung
common injury: radial nerve in spiral groove
lesioned by midshaft fracture of humerus
common injury: radial nerve on medial arm
compressed in axilla by improper use of crutches
common injury: radial nerve (deep branch)
stretched by subluxation of the radius
common injury: median nerve
compressed by supracondylar fracture of humerus:
pronator teres syndrome
common injury: ulnar nerve
lesioned by repeated minor trauma,
fracture of medial epicondyle of humerus
common injury: anterior interosseous nerve
compressed in deep forearm
common injury: recurrent branch of median nerve
lesioned by superficial laceration to thenar eminence
common injury: ulnar nerve in hand
lesioned by trauma to hypothenar eminence
fracture to hook of hamate
Brachial plexus lesions:

Waiter's tip (Erb's palsy)
lesion to upper trunk (C5, C6)
Brachial plexus lesions:

total claw hand (Klumpke's palsy)
lesion to lower trunk (C8, T1)
Brachial plexus lesions:

wrist drop
lesion to posterior cord (C7)
Brachial plexus lesions:

winged scapula
long thoracic nerve
Brachial plexus lesions:

deltoid paralysis
axillary nerve lesion (C7)
Brachial plexus lesions:

Saturday night palsy (wrist drop)
radial nerve lesion (C7)
Brachial plexus lesions:

difficulty flexing elbow,
variable sensory loss
musculocutaneous nerve (C5, C6)
Brachial plexus lesions:

decreased thumb function ("ape hand"), "Pope's blessing"
median nerve (C5, C6, C8, T1)
Brachial plexus lesions:

intrinsic muscles of hand,
claw hand
ulnar nerve (C8, T1)
Etiology & appearance: Erb-Duchenne Palsy
Traction or tear of upper trunk (C5, C6)
follows blow to shoulder or perinatal trauma

findings:
- paralysis of abductors
- paralysis of lateral rotators (constant medial rotation)
- loss of biceps (forearm pronated)
Klumpke's palsy
embryologic or perinatal defect affecting inferior trunk (C8, T1)
cervical rib compresses subclavian artery & inferior turnk, resulting in
THORACIC OUTLET SYNDROME
Thoracic Outlet Syndrome - findings
atrophy of thenar and hypothenar eminences
atrophy of interosseus muscles
sensory deficits on medial side of forearm and hand
disappearance of radial pulse upon moving head toward opposite side
Distortions of the hand involve which muscle group?
Lumbricals - flex MCP and extend DIP/PIP
Ulnar claw
distal ulnar nerve lesion -->
loss of medial lumbrical function
4th & 5th digits are clawed "Pope's blessing"
Median claw
Distal median nerve lesion
loss of lateral lumbrical function
2nd & 3rd digits clawed
"Ape hand"
proximal median nerve lesion
loss of opponens pollicis muscle function
unopposable thumb (inability to abduct thumb)
Klumpke's total claw
Lesion of lower trunk (C8, T1)
loss of function of all lumbricals;

forearm finger flexors (C5-C7) & finger extensors (radial n) unopposed -->

clawing of all digits
"Great extensor nerve"
radial nerve
Radial nerve innervates which four muscles:
BEST!

Brachioradialis
Extensors of wrist and fingers
Supinator
Triceps
Muscles of Thenar eminence
Opponens pollicis
Abductor pollicis brevis
Flexor pollicis brevis
Muscles of Hypothenar eminence
Opponens digitis minimi
Abductor digiti minimi
Flexor digiti minimi
Function: dorsal interosseious muscles
abduct the fingers
Function: palmar interosseous muscles
adduct fingers
Function: lumbrical muscles
flex at MP joint
Repetitive elbow trauma
degenerative injury due to repeated use
leads to tiny tears in tendons in muscles
may be inflammatory,
e.g.: lateral epicondylitis (tennis elbow)
medial epicondylitis (golf elbow)
Lateral epicondylitis
tennis elbow
medial epicondylitis
golf elbow
Nerve: obdurator
Cause of injury:
Motor deficit:
Sensory deficit
Nerve: Obdurator
Cause of injury: anterior hip dislocation
Motor deficit: thigh adduction
Sensory deficit: medial thigh
Nerve: femoral
Cause of injury:
Motor deficit:
Sensory deficit:
Nerve: femoral
Cause of injury: pelvic fracture
Motor deficit: thigh flexion, leg extension
Sensory deficit: anterior thigh & medial leg
Nerve: common peroneal
Cause of injury:
Motor deficit:
Sensory deficit:
Nerve: common peroneal
Cause of injury: trauma to lateral aspect of leg or fibular neck fracture
Motor deficit: foot eversion, dorsiflexion; toe extension
Sensory deficit: anterolateral leg, dorsal foot
Nerve: tibial
Cause of injury:
Motor deficit:
Sensory deficit:
Nerve: tibial
Cause of injury: knee trauma
Motor deficit: foot inversion, plantarfelxion, toe flexion
Sensory deficit: sole of foot
Nerve: inferior gluteal
Cause of injury:
Motor deficit:
Sensory deficit:
Nerve: inferior gluteal
Cause of injury: posterior hip dislocation
Motor deficit: can't jump, climb stairs, rise from seated position
Sensory deficit: none
Muscle contraction
review First Aid pages 356 - 7
Endochondral ossification
longitudinal bone growth
cartilaginous model from chondrocytes
osteocasts & osteoblasts replace with woven bone, remodel to lamellar bone
Membranous ossification
flat bone growth (skull, facial bones, axial skeleton)
woven bone formed directly without cartilage
later remodelled to lamellar bone
Osteoporosis
- sequellae
- prophylaxis
- treatment
Osteoporosis
Sequellae:
- vertebral crush fractures (acute back pain, loss of height, kyphosis)
- distal radius (Colles') fractures
- vertebral wedge fractures

Prophylaxis:
- exercise
- dietary calcium before age 30

Treatment:
- estrogen &/or calcitonin
- biphosphonates or pulsatile PTH for severe cases
Osteopetrosis
- etiology
- lab values
- sequellae
- radiography
Osteopetrosis
Etiology:
- failure normal osteoclastic bone resorption --> thickened, dense bones
- genetic deficiency carbonic anhydrase II

Lab values:
- Ca2+, PO4(3-), Alk. Phos. = NORMAL

Sequellae:
- decreased marrow space leads to anemia, thrombocytopenia, infection
- flared bones can case CN impingement, palsies 2* narrowed foramina

Xrays show "Erlenmeyer flask" bones that flare out
Osteomalacia
Soft bones 2* defective mineralization/calcification of osteoid

Vitamin D deficiency in adults -->
decreased calcium levels -->
increased PTH secretion & decreased serum phosphate

reversible when vitamin D is replaced
RIckets
Vitamin D deficiency in childhood
Osteitis fibrosa cystica
- histology
- serum levels (Ca, P, ALP)
caused by hyperparathyroidism
characterized by "brown tumors"
- cystic spaces lined by osteoclasts, filled with fibrous stroma and sometimes blood

Serum levels:
- high calcium,
- low phosphorus,
- high ALP
Paget's disease (osteitis deformans)
abnormal bone architecture caused by increased in both osteoblastic and osteoclastic activity

possibly viral in origin (paramyxovirus?)

Serum, Ca, P, PTH levels normal

Increased ALP

Mosaic bone pattern
Long bone chalk-stick fractures
Increased blood flow from increased AV shunts may cause high-output CHF

Can lead to osteogenic sarcoma
Osteoporosis:
Serum Ca2+:
Phophate:
ALP:
PTH:
Other:
Osteoporosis
Serum Ca2+: normal
Phophate: normal
ALP: normal
PTH: normal
Other: decreased bone mass
Osteopetrosis:
Serum Ca2+:
Phophate:
ALP:
PTH:
Other:
Osteopetrosis:
Serum Ca2+: normal
Phophate: normal
ALP: normal
PTH: normal
Other: thickened, dense bones
Osteomalacia/rickets
Serum Ca2+:
Phophate:
ALP:
PTH:
Other:
Osteomalacia/rickets:
Serum Ca2+: decreased
Phophate: decreased
ALP: normal
PTH: increased
Other: soft bones
Osteitis fibrosa cystica:
Serum Ca2+:
Phophate:
ALP:
PTH:
Other:
Osteitis fibrosa cystica:
Serum Ca2+: increased
Phophate: decreased
ALP: increased
PTH: increased
Other: "brown tumors"
Paget's disease
Serum Ca2+:
Phophate:
ALP:
PTH:
Other:
Paget's disease
Serum Ca2+: normal
Phophate: normal
ALP: increased
PTH: normal
Other: abnormal bone architecture
Polyostotic fibrous dysplasia
bone replaced by fibroblasts, collagen, irregular bony trabeculae
affects many bones

variation: Mc-Cune Albright syndrome
McCune Albright syndrome
form of polyostotic fibrous dysplasia
multiple unilateral bone lesion
endocrine abnormalities (precocious puberty)
unilateral pigemented skin lesions (café-au-lait spots)
Osteoma
Benign bone tumor
associated with Gardner's syndrome (FAP)
new piece of bone grows on another bone, often in skull
Osteoid osteoma
Benign bone tumor
interlacing trabeculae of woven bone
surrounded by osteobasts
< 2 cm
proximal tibial & femur
most common in men < 25 y/o
Osteoblastoma
same morphologically as osteoid osteoma,
but larger and found in vertebral column
Giant cell tumor
occurs moly at epiphyseal end of long bones
peak incidence 20-40 y.o
locally aggressive
often in distal femur, proximal tibia
characteristic "double bubble" or "soap bubble" appearance on x-ray
spindle-shaped cells with multinucleated giant cells
Osteochondroma
most common benign bone tumor
mature bone with cartilaginous cap
usually in men < 25 y/o
commonly originates from long metaphysis
Endochondroma
benign cartilaginous neoplasm
intramedullary bone
usually distal extremities (vs. chondromsarcoma)
Osteosarcoma
Malignant bone tumor
2nd most common 1* malignant tumor of bone
peak incidence: men 10-20 y/o
commonly found in metaphysis of long bones, around knee

Codman's triangle (sunburst pattern from elevation of periosteum) on xray
predisposing factors:
- Paget's
- bone infarcts
- radiation
- familial retinoblastoma

Poor prognosis
Ewing's sarcoma
Anaplastic small blue cell malignant tumor
most common in boys < 15 y/o
extremely aggressive with early metastases
responsive to chemo
characteristic onion-skin appearance in bone
commonly in diaphysis of long bones, pelvis, scapula, ribs
11;22 translocation
Chondrosarcoma
malignant cartilaginous tumor
most common in men 30-60 y.o
usually in pelvis, spine, scapula, humerus, tibia, femus
expansile glistening mass in medullary cavity
Primary bone tumor: epiphysis
Benign: giant cell tumor (osteoclastoma)
Malignant: N/A
Primary bone tumor: metaphysis
Benign: osteochondroma
Malignant: osteosarcoma
Primary bone tumor: diaphysis
Benign: osteoid osteoma
Malignant: Ewing's sarcoma
Primary bone tumor: intramedullary
Benign: enchondroma
Malignant: chondrosarcoma
Osteoarthritis
review p. 361
RA
review p. 362
Sjorgren's syndrome:
Classic triad -
Other symptoms -
Epidemiology -
Sjorgren's syndrome
Classic triad -
(1) xerophthalmia (dry eyes, conjunctivitis, "sand in my eyes")
(2) xerostomia (dry mouth, dyphagia)
(3) arthritis

Other symptoms:
- parotid enlargement
- increased risk B cell lymphoma
- dental caries
- autoantibodies to ribonucleoprotein antigens (SS-A (Ro), SS-B (La))

usu. in females 40-60 y.o
associated with RA
Sicca syndrome
like Sjorgren's, but without arthritis:

dry eyes, dry mouth, anal and vaginal dryness, chronic bronchitis, reflex esophagitis
gout & pseudogout
review p. 363
Infectious arthrtis: septic
S. aureus, Streptococcus, N. gonorrhoeae

affected joint is swollen, red, painful
Gonococcal arthritis
presents as monoarticular, migratory arthritis with asymmetrical pattern
Infectious arthritis: chronic
TB
Lyme disease
Seronegative spondyloarthropathies
review p. 364
SLE
review p. 364
Polymyositis/dermatomyositis: symptoms of polymyositis
progressive symmetric proximal muscle weakness
caused by CD8+ T cell induced injury to myofibers
most often involves shoulders
mucle biopsy with evidence of inflammation is diagnostic
Polymyositis/dermatomyositis: symptoms of dermatomyositis
similar to polymyositis
also invovles malar rash, heliotrope rash, shawl & face rash, Gottron's papules
increased risk malignancy
Polymyositis/dermatomyositis: lab findings (both)
increased CK
increased aldolase
(+) ANA
(+) anti-Jo-I
Polymyositis/dermatomyositis: treatments
steroids
NMJ diseases (2)
Myasthenia gravis
Lambert-Eaton syndrome
Myasthenia gravis
most common NMJ disorder
AutoAbs to postsynamptic AChR
ptosis, diplopia, general weakness
associated with thymoma
symptoms worsen with muscle use
reversal of symptoms with AChE inhibitors
Lambert-Eaton syndrome
Autoantibodies to presynaptic Ca2+ channel results in decreased ACh release
--> proximal muscle weakness
associated with paraneoplastic diseases (e.g.: small cell lung CA)
symptoms improve with msucle use
no reversal of symptoms with AChE inhibitors alone
sarcoidosis
review. p. 365
polymyalgia rhematica
rev. p. 365
mixed CT ds
rev. -. 365
Scleroderma: general
aka: progressive systemic sclerosis (PSS)
excessive fibrosis and colalgen deposition througout body
commonly sclerosis of skin
manifests as puffy and taught w/ absence of wrinkles
also sclerosis of renal, pulmonary, CV, GI systems
75% female
Scleroderma: diffuse scleroderma
widespread skin involvement,
rapid progression
early visceral involvement
associated with Anti-Scl-70 Ab (antiDNA topoisomerase I Ab)
Scleroderma: CREST syndrome
Calcinosis
Raynaud's phenomenon
Esophageal dysmotility
Sclerodactyly
Telangiectasia

Limited skin involvement, oft. confined to fingers & face
more benign clinical course
assicated with antiCentrimere antibody
Aspirin: mechanism
irreversibly inhibits COX by covalent binding
--> decreased synthesis of TX & PG
Aspirin: clinical use
low dose (> 300 mg/day) decreases platelet aggregation

intermediate dose (300-2400 mg/day): antipyretic & analgesic

high dose (2400-4000 mg/day): anti-inflammatory
NSAIDs: names
ibuprofen
naproxen
indomethacin
ketorlac
NSAIDs: mechanism
reversibly inhibit COX
block PG synthesis
NSAIDs: clinical use
antipyretic
analgesic
anti-inflammatory
Aspirin: toxicity
gastric upset
chronic use can lead to
- acute renal failure
- interstitial nephritis
- upper GI bleeds

Reye's syndrome in children with viral infection
NSAIDs: toxicity
renal damage
aplastic anemia
GI distress
ulcers
COX-2 inhibitors: names
celecoxib
COX-2 inhibitors: mechanism
reversilby inhibit COX-2 (spares COX-1)
COX-2 found in inflammatory cells, vascular endothelium
COX-2 inhibitors: clinical use
RA
OA
COX-2 inhibitors: toxicity
increased risk thrombosis
sulfa allergy
acetaminophen: mechanism
reversibly inhibits COX, mostly in CNS
inactivated peripherally
acetaminophen: clinical use
antipyretic
analgesic
lacks anti-inflammatory properties
used instead of ASA in children
acetaminophen: : toxicity
overdose --> hepatic necrosis
- acetaminophen metabolite depletes glutathione, forms toxic tissue adducts in liver

N-actetylcystein is antidote - regenerates glutathione
Bisphosphonates: names
etidronate
pamidronate
alendronate
risedronate
Bisphosphonates: mechanism
inhibit osteoCLASTIC activity
reduce both formation & resorption of hydroxyapatite
Bisphosphonates: clinical use
malignancy-associated hypercalcemia
Paget's disease of bone
post-menopausal osteoporosis
Bisphosphonates: toxicity
corrosive esophagitis
nausea
diarrhea
Colchicine: mechanism
depolymerizes microtubules,
impariing WBC chemotaxis & degranulation
Colchicine: clinical use
chronic gout
Colchicine: toxicity
GI effects, esp. if given orally
(N.B.: indomethacin is less toxic, used in acute gout)
Probenecid: mechanism
inhibits reabsorption of uric acid in PCT (proximal tubule)
Probenecid: clinical use
chronic gout
Probenecid: toxcity
inhibits secretion of penicillin
Allopurinol: mechanism
inhibits xanthine oxidase
decreased conversion of xanthine to uric acid
increases concentration of azathrioprine & 6-MP (usu. metabolized by xanthine oxidase)
Bisphosphonates: mechanism
inhibit osteoCLASTIC activity
reduce both formation & resorption of hydroxyapatite
Bisphosphonates: clinical use
malignancy-associated hypercalcemia
Page's disease of bone
post-menopausal osteoporosis
Bisphosphonates: toxicity
corrosive esophagitis
nausea
diarrhea
Colchicine: mechanism
depolymerizes microtubules,
impariing WBC chemotaxis & degranulation
Colchicine: clinical use
chronic gout
Colchicine: toxicity
GI effects, esp. if given orally
(N.B.: indomethacin is less toxic, used in acute gout)
Probenecid: mechanism
inhibits reabsorption of uric acid in PCT (proximal tubule)
Probenecid: clinical use
chronic gout
Probenecid: toxcity
inhibits secretion of penicillin
Allopurinol: mechanism
inhibits xanthine oxidase
decreased conversion of xanthine to uric acid
increases concentration of azathrioprine & 6-MP (usu. metabolized by xanthine oxidase)
Allopurinol: clinical use
chronic gout
prevention of urate nephropathy 2* tumor lysis syndrome
2 drugs NOT to use in acute gout
allopurinol
probenecid
Drug class NOT to give for gout, ever
salicylates
all but the highest doses depress uric acid clearance
Etanercept: mechanism
recombinant form of human TNF receptor that binds TNF
Etanercept: clinical use
RA
psoriasis
ankylosing spondylitis
Infliximab: mechanism
Anti-TNF antibody
Infliximab: clinical use
Chrohn's disease
RA
ankylosing spondylitis
Infliximab: toxicity
predisposes to infection (reactivation of latent TB)
Nerve: superior gluteal
Cause of injury:
Motor deficit:
Sensory deficit
Nerve: superior gluteal
Cause of injury: posterior hip dislocation or polio
Motor deficit:thigh abduction [(+) Trendelenburg sign]
Sensory deficit: none