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144 Cards in this Set
- Front
- Back
The injury called the "unholy triad"
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damage to:
- MCL - medial meniscus - ACL |
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Positive anterior drawer sign indicates...
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torn ACL
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abnormal passive abduction indicates...
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torn MCL
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Shoulder muscles that form rotator cuff and their functions
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Supraspinatus - ABducts arm (helps deltoid)
Infraspinatus - laterally rotates arm Teres minor - adducts and laterally rotates arm Subscapularis - medially rotates and adducts arm |
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Common injury: upper trunk
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lesioned by trauma
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common injury: C7 root
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compressed by cervical disc lesion
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common injuries (3): axillary nerve
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lesioned by
- fracture of surgical neck of humerus - dislocation of humerus - intramuscular injections |
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common injuries (2): lower trunk of brachial plexus
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compressed by cervical rib
or by Pancoast tumor of lung |
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common injury: radial nerve in spiral groove
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lesioned by midshaft fracture of humerus
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common injury: radial nerve on medial arm
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compressed in axilla by improper use of crutches
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common injury: radial nerve (deep branch)
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stretched by subluxation of the radius
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common injury: median nerve
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compressed by supracondylar fracture of humerus:
pronator teres syndrome |
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common injury: ulnar nerve
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lesioned by repeated minor trauma,
fracture of medial epicondyle of humerus |
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common injury: anterior interosseous nerve
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compressed in deep forearm
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common injury: recurrent branch of median nerve
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lesioned by superficial laceration to thenar eminence
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common injury: ulnar nerve in hand
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lesioned by trauma to hypothenar eminence
fracture to hook of hamate |
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Brachial plexus lesions:
Waiter's tip (Erb's palsy) |
lesion to upper trunk (C5, C6)
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Brachial plexus lesions:
total claw hand (Klumpke's palsy) |
lesion to lower trunk (C8, T1)
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Brachial plexus lesions:
wrist drop |
lesion to posterior cord (C7)
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Brachial plexus lesions:
winged scapula |
long thoracic nerve
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Brachial plexus lesions:
deltoid paralysis |
axillary nerve lesion (C7)
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Brachial plexus lesions:
Saturday night palsy (wrist drop) |
radial nerve lesion (C7)
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Brachial plexus lesions:
difficulty flexing elbow, variable sensory loss |
musculocutaneous nerve (C5, C6)
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Brachial plexus lesions:
decreased thumb function ("ape hand"), "Pope's blessing" |
median nerve (C5, C6, C8, T1)
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Brachial plexus lesions:
intrinsic muscles of hand, claw hand |
ulnar nerve (C8, T1)
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Etiology & appearance: Erb-Duchenne Palsy
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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) |
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Klumpke's palsy
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embryologic or perinatal defect affecting inferior trunk (C8, T1)
cervical rib compresses subclavian artery & inferior turnk, resulting in THORACIC OUTLET SYNDROME |
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Thoracic Outlet Syndrome - findings
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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 |
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Distortions of the hand involve which muscle group?
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Lumbricals - flex MCP and extend DIP/PIP
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Ulnar claw
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distal ulnar nerve lesion -->
loss of medial lumbrical function 4th & 5th digits are clawed "Pope's blessing" |
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Median claw
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Distal median nerve lesion
loss of lateral lumbrical function 2nd & 3rd digits clawed |
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"Ape hand"
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proximal median nerve lesion
loss of opponens pollicis muscle function unopposable thumb (inability to abduct thumb) |
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Klumpke's total claw
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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 |
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"Great extensor nerve"
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radial nerve
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Radial nerve innervates which four muscles:
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BEST!
Brachioradialis Extensors of wrist and fingers Supinator Triceps |
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Muscles of Thenar eminence
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Opponens pollicis
Abductor pollicis brevis Flexor pollicis brevis |
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Muscles of Hypothenar eminence
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Opponens digitis minimi
Abductor digiti minimi Flexor digiti minimi |
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Function: dorsal interosseious muscles
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abduct the fingers
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Function: palmar interosseous muscles
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adduct fingers
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Function: lumbrical muscles
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flex at MP joint
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Repetitive elbow trauma
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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) |
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Lateral epicondylitis
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tennis elbow
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medial epicondylitis
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golf elbow
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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 |
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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 |
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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 |
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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 |
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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 |
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Muscle contraction
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review First Aid pages 356 - 7
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Endochondral ossification
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longitudinal bone growth
cartilaginous model from chondrocytes osteocasts & osteoblasts replace with woven bone, remodel to lamellar bone |
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Membranous ossification
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flat bone growth (skull, facial bones, axial skeleton)
woven bone formed directly without cartilage later remodelled to lamellar bone |
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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 |
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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 |
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Osteomalacia
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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 |
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RIckets
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Vitamin D deficiency in childhood
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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 |
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Paget's disease (osteitis deformans)
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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 |
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Osteoporosis:
Serum Ca2+: Phophate: ALP: PTH: Other: |
Osteoporosis
Serum Ca2+: normal Phophate: normal ALP: normal PTH: normal Other: decreased bone mass |
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Osteopetrosis:
Serum Ca2+: Phophate: ALP: PTH: Other: |
Osteopetrosis:
Serum Ca2+: normal Phophate: normal ALP: normal PTH: normal Other: thickened, dense bones |
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Osteomalacia/rickets
Serum Ca2+: Phophate: ALP: PTH: Other: |
Osteomalacia/rickets:
Serum Ca2+: decreased Phophate: decreased ALP: normal PTH: increased Other: soft bones |
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Osteitis fibrosa cystica:
Serum Ca2+: Phophate: ALP: PTH: Other: |
Osteitis fibrosa cystica:
Serum Ca2+: increased Phophate: decreased ALP: increased PTH: increased Other: "brown tumors" |
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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 |
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Polyostotic fibrous dysplasia
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bone replaced by fibroblasts, collagen, irregular bony trabeculae
affects many bones variation: Mc-Cune Albright syndrome |
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McCune Albright syndrome
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form of polyostotic fibrous dysplasia
multiple unilateral bone lesion endocrine abnormalities (precocious puberty) unilateral pigemented skin lesions (café-au-lait spots) |
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Osteoma
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Benign bone tumor
associated with Gardner's syndrome (FAP) new piece of bone grows on another bone, often in skull |
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Osteoid osteoma
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Benign bone tumor
interlacing trabeculae of woven bone surrounded by osteobasts < 2 cm proximal tibial & femur most common in men < 25 y/o |
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Osteoblastoma
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same morphologically as osteoid osteoma,
but larger and found in vertebral column |
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Giant cell tumor
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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 |
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Osteochondroma
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most common benign bone tumor
mature bone with cartilaginous cap usually in men < 25 y/o commonly originates from long metaphysis |
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Endochondroma
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benign cartilaginous neoplasm
intramedullary bone usually distal extremities (vs. chondromsarcoma) |
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Osteosarcoma
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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 |
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Ewing's sarcoma
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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 |
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Chondrosarcoma
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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 |
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Primary bone tumor: epiphysis
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Benign: giant cell tumor (osteoclastoma)
Malignant: N/A |
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Primary bone tumor: metaphysis
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Benign: osteochondroma
Malignant: osteosarcoma |
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Primary bone tumor: diaphysis
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Benign: osteoid osteoma
Malignant: Ewing's sarcoma |
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Primary bone tumor: intramedullary
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Benign: enchondroma
Malignant: chondrosarcoma |
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Osteoarthritis
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review p. 361
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RA
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review p. 362
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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 |
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Sicca syndrome
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like Sjorgren's, but without arthritis:
dry eyes, dry mouth, anal and vaginal dryness, chronic bronchitis, reflex esophagitis |
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gout & pseudogout
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review p. 363
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Infectious arthrtis: septic
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S. aureus, Streptococcus, N. gonorrhoeae
affected joint is swollen, red, painful |
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Gonococcal arthritis
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presents as monoarticular, migratory arthritis with asymmetrical pattern
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Infectious arthritis: chronic
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TB
Lyme disease |
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Seronegative spondyloarthropathies
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review p. 364
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SLE
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review p. 364
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Polymyositis/dermatomyositis: symptoms of polymyositis
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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 |
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Polymyositis/dermatomyositis: symptoms of dermatomyositis
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similar to polymyositis
also invovles malar rash, heliotrope rash, shawl & face rash, Gottron's papules increased risk malignancy |
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Polymyositis/dermatomyositis: lab findings (both)
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increased CK
increased aldolase (+) ANA (+) anti-Jo-I |
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Polymyositis/dermatomyositis: treatments
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steroids
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NMJ diseases (2)
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Myasthenia gravis
Lambert-Eaton syndrome |
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Myasthenia gravis
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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 |
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Lambert-Eaton syndrome
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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 |
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sarcoidosis
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review. p. 365
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polymyalgia rhematica
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rev. p. 365
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mixed CT ds
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rev. -. 365
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Scleroderma: general
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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 |
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Scleroderma: diffuse scleroderma
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widespread skin involvement,
rapid progression early visceral involvement associated with Anti-Scl-70 Ab (antiDNA topoisomerase I Ab) |
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Scleroderma: CREST syndrome
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Calcinosis
Raynaud's phenomenon Esophageal dysmotility Sclerodactyly Telangiectasia Limited skin involvement, oft. confined to fingers & face more benign clinical course assicated with antiCentrimere antibody |
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Aspirin: mechanism
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irreversibly inhibits COX by covalent binding
--> decreased synthesis of TX & PG |
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Aspirin: clinical use
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low dose (> 300 mg/day) decreases platelet aggregation
intermediate dose (300-2400 mg/day): antipyretic & analgesic high dose (2400-4000 mg/day): anti-inflammatory |
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NSAIDs: names
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ibuprofen
naproxen indomethacin ketorlac |
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NSAIDs: mechanism
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reversibly inhibit COX
block PG synthesis |
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NSAIDs: clinical use
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antipyretic
analgesic anti-inflammatory |
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Aspirin: toxicity
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gastric upset
chronic use can lead to - acute renal failure - interstitial nephritis - upper GI bleeds Reye's syndrome in children with viral infection |
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NSAIDs: toxicity
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renal damage
aplastic anemia GI distress ulcers |
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COX-2 inhibitors: names
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celecoxib
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COX-2 inhibitors: mechanism
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reversilby inhibit COX-2 (spares COX-1)
COX-2 found in inflammatory cells, vascular endothelium |
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COX-2 inhibitors: clinical use
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RA
OA |
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COX-2 inhibitors: toxicity
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increased risk thrombosis
sulfa allergy |
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acetaminophen: mechanism
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reversibly inhibits COX, mostly in CNS
inactivated peripherally |
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acetaminophen: clinical use
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antipyretic
analgesic lacks anti-inflammatory properties used instead of ASA in children |
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acetaminophen: : toxicity
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overdose --> hepatic necrosis
- acetaminophen metabolite depletes glutathione, forms toxic tissue adducts in liver N-actetylcystein is antidote - regenerates glutathione |
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Bisphosphonates: names
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etidronate
pamidronate alendronate risedronate |
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Bisphosphonates: mechanism
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inhibit osteoCLASTIC activity
reduce both formation & resorption of hydroxyapatite |
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Bisphosphonates: clinical use
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malignancy-associated hypercalcemia
Paget's disease of bone post-menopausal osteoporosis |
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Bisphosphonates: toxicity
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corrosive esophagitis
nausea diarrhea |
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Colchicine: mechanism
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depolymerizes microtubules,
impariing WBC chemotaxis & degranulation |
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Colchicine: clinical use
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chronic gout
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Colchicine: toxicity
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GI effects, esp. if given orally
(N.B.: indomethacin is less toxic, used in acute gout) |
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Probenecid: mechanism
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inhibits reabsorption of uric acid in PCT (proximal tubule)
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Probenecid: clinical use
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chronic gout
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Probenecid: toxcity
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inhibits secretion of penicillin
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Allopurinol: mechanism
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inhibits xanthine oxidase
decreased conversion of xanthine to uric acid increases concentration of azathrioprine & 6-MP (usu. metabolized by xanthine oxidase) |
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Bisphosphonates: mechanism
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inhibit osteoCLASTIC activity
reduce both formation & resorption of hydroxyapatite |
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Bisphosphonates: clinical use
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malignancy-associated hypercalcemia
Page's disease of bone post-menopausal osteoporosis |
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Bisphosphonates: toxicity
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corrosive esophagitis
nausea diarrhea |
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Colchicine: mechanism
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depolymerizes microtubules,
impariing WBC chemotaxis & degranulation |
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Colchicine: clinical use
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chronic gout
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Colchicine: toxicity
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GI effects, esp. if given orally
(N.B.: indomethacin is less toxic, used in acute gout) |
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Probenecid: mechanism
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inhibits reabsorption of uric acid in PCT (proximal tubule)
|
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Probenecid: clinical use
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chronic gout
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Probenecid: toxcity
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inhibits secretion of penicillin
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Allopurinol: mechanism
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inhibits xanthine oxidase
decreased conversion of xanthine to uric acid increases concentration of azathrioprine & 6-MP (usu. metabolized by xanthine oxidase) |
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Allopurinol: clinical use
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chronic gout
prevention of urate nephropathy 2* tumor lysis syndrome |
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2 drugs NOT to use in acute gout
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allopurinol
probenecid |
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Drug class NOT to give for gout, ever
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salicylates
all but the highest doses depress uric acid clearance |
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Etanercept: mechanism
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recombinant form of human TNF receptor that binds TNF
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Etanercept: clinical use
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RA
psoriasis ankylosing spondylitis |
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Infliximab: mechanism
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Anti-TNF antibody
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Infliximab: clinical use
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Chrohn's disease
RA ankylosing spondylitis |
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Infliximab: toxicity
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predisposes to infection (reactivation of latent TB)
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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 |