MSK Flashcards

(125 cards)

1
Q

Risk factors for carpal tunnel syndrome

A
pregnancy
RA
DM
Acromegaly
hypothyroidism
obesity
overuse

age 30-55
more common in females

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2
Q

Carpal tunnel syndrome H and P

A
H and P
hand numbness and tingling
wrist pain that radiates up the arm
dropped objects
decreased hand strength
decreased palmar 2-point discrimination

thenal muscle atrophy

Tinel sign
Phalen sign (hold for about a minute)

EMG and nerve- conduction studies for definitive diagnosis

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3
Q

Carpal tunnel syndrome treatment

A
wrist spiints
activity modification
NSAIDs
steroid injections
surgical release of transverse carpal ligament
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4
Q

Shoulder dislocation

A

anterior is most common

humeral head comes forward and tears the anterior labrum of the shoulder

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5
Q

Treatment for anterior shoulder dislocation

A

pain control, then closed reduction, then immobilize with a sling and have the patient follow up with an orthopedic surgeon

Pain control: lidocaine, narcotics, conscious sedation

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6
Q

Bankart lesion

A

anterior labrum is torn 2/2 anterior dislocation

90% of anterior dislocations
Repair may prevent future dislocation

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7
Q

Posterior hip dislocation

A

posteriorly directed force on internally rotated, flexed, adducted hip

Treatment: 
closed reduction
bracing
abduction pillow
confirm normal alignment with xray, without chips of bone in the socket
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8
Q

nerve damage implicated in claw hand

A

ulnar nerve

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9
Q

ape hand

A

median nerve

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10
Q

wrist drop

A

radial nerve

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11
Q

scapular winging

A

Long thoracic nerve

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12
Q

unable to wipe bottom

A

thoracodorsal nerve

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13
Q

loss of forearm pronation

A

median nerve

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14
Q

cannot abduct or adduct fingers

A

ulnar nerve

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15
Q

loss of shoulder abduction

A

axillary nerve

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16
Q

weak external rotation of arm

A

suprascapular nerve, axillary nerve

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17
Q

loss of elbow flexion and forearm supination

A

musculocutaneous nerve

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18
Q

loss of wrist extension

A

radial nerve

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19
Q

trouble initiating shoulder abduction

A

suprascapular nerve

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20
Q

unable to abduct arm beyond 10 degrees

A

axillary nerve

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21
Q

unable to raise arm above horizontal

A

long thoracic nerve

spinal accessory nerve

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22
Q

fracture of humoral shaft puts what nerve at risk?

A

radial nerve

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23
Q

fracture of surgical neck of humerus puts what nerve at risk?

A

axillary nerve

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24
Q

supracondylar fracture puts what nerve at risk?

A

median nerve

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25
medial epicondyle fracture puts what nerve at risk?
ulnar nerve
26
anterior shoulder dislocation puts what nerve at risk?
axillary nerve
27
Colles fracture
distal radius +/- distal ulna associated with osteoporosis Treatment: long cast to immobilize the wrist and elbow (immobilize the joint above and below the fracture)
28
Smith fracture
fracture of distal radius with anterior displacement MOI: fall and land on flexed wrist less common than Colles
29
Scaphoid fracture
fall on radially deviated outstretched hand tenderness in snuffbox indicates scaphoid fracture until proven otherwise Treatment: immobilization of wrist with spica cast poor union rate even when treated correctly, with risk of avascular necrosis
30
Boxer's fracture
MOI: punching a wall force transferred to 5th metacarpal Treat: closed reduction surgical pinning open wounds from teeth require surgical exploration to rule out tendon involvement Copious irrigation
31
Monteggia fracture
dislocation of radial head and ulnar diaphyseal fracture defense injuries falls on outstretched hand with forearm in excessive pronation Treatment: surgery
32
Nightstick injury
isolated ulnar shaft fracture Treatment: does not require surgery
33
Galeazzi fracture (DRUJ)
distal radial ulnar joint dislocation and radial diaphyseal fracture Treatment: this will require surgery
34
Hip fracture
intratrochanteric subtrochanteric increased risk for avascular necrosis with femoral neck fractures H and P: injured leg is shortened and externally rotated
35
Femur fractures
Caused by severe trauma Treatment: surgery Increased risk for fat embolizatin - hypoxemia - petechiae serial H/H compartment syndrome exams secondary survey as indicated by MOI XRay, CT, spinal immobilization
36
Tibial fracture
increased risk for compartment syndrome
37
Ankle fracture
if unstable, then requires operative stabilization
38
Pelvic fracture
high risk of major blood loss decreased pelvic volume If hypotensive and can't find blood in pelvis, consider retroperitoneal hemorrhage (angiogram to diagnose, then embolize if you find retroperitoneal)
39
Sprain
injury to ligaments and soft tissues surrounding a joint Partial or complete tear at the ligament- bone interface Grade 1: overstretching of muscles with microscopic tears Grade 2:incomplete tear Grade 3: complete tear pain with weightbearing and movement ankle and knee are most common Rest Ice Compression Elevation
40
Ligament tear
ACL, PCL Anterior drawer Lachman MRI for soft tissue CT for bone
41
Unhappy triad
medially- directed blow to lateral side of knee Structures injured: ACL tear MCL tear Lateral meniscus tear
42
Meniscus tears
H and P: vague pain inside knee clicking or locking joint line pain near knee Radiology: MRI Treatment: NSAIDS PT Arthroscopic repair for debridement Complications: Debridement puts the patient at risk for osteoarthritis
43
most commonly injured knee ligament
MCL
44
positive Lachman test
ACL
45
Positive McMurray test aids in diagnosis
Meniscus tear
46
common dashboard injury in an MVA
PCL
47
Compartment syndrome
``` Late manifestations: Pain Pallor Poikilothermia Pulselessness Paralysis Paresthesias ``` Sensitive screening test: Compartment pain with passive stretching, pain in excess of what is expected Diagnosis: Manometry needle placed into the muscle, greater than 30mmHg makes the diagnosis also treat if within 20mmHg of diastolic BP Most common compartments involved: volar compartment of forearm, anterior compartment of leg Most commonly due to fractures (supracondylar humerus, both- bones of forearm, proximal tibia) Treatment: emergency fasciotomy of ALL the compartments involved and not just the one compartment exertional compartment syndrome can happen in young athletes, and resolves with rest, minimal risk of ischemia
48
Back pain radiating to epigastrium while eating
PUD, GERD, gastritis
49
Back pain radiating to epigastrium with elevated amylase/lipase
pancreatitis
50
Back pain radiating to epigastrium with pulsatile mass
triple A
51
Back pain radiating to pelvis and hematuria
renal stones
52
Back pain radiating to pelvis and CVA tenderness
pyelonephritis
53
Back pain only along spine along paraspinals
muscle strain (don't want patient to be completely inactive)
54
Back pain only along spine with osteoporosis
compression fracture
55
Back pain only along spine with back asymmetry
scoliosis
56
Back pain only along spine with abnormal gait (knees/hips flexed)
anterior slip of disk (spondylolisthesis)
57
Back pain only along spine along with systemic signs of infection
meningitis discitis osteomyelitis
58
Back pain (radiating) or new neuro symptoms worse with exertion
disc herniation
59
Back pain (radiating) or new neuro symptoms and pain with walking or standing
spinal stenosis
60
Back pain (radiating) or new neuro symptoms worse with rest, better with activity
ankylosing spondylitis | young male, 20's, 30's
61
Back pain (radiating) or new neuro symptoms all day
cancer
62
Back pain (radiating) or new neuro symptoms with bowel/bladder dysfunction, saddle area anesthesia
cauda equina syndrome
63
degenerative disc disease
radiculopathy H and P: - pain extends along path of compressed nerve - sensory and motor deficits - pain worsens with straight leg raises or Valsalva MRI will allow you to diagnose ``` Treatment: NSAIDs Activity modification epidural steroid injection surgical decompression ``` Neuropathic pain: Gabapentin Pregabalin Depression + neuropathic pain Duloxetine
64
Spinal stenosis
generalized narrowing of the bony spaces in the spine 2.2 arthritic changes older adults H and P: radiating pain worse with walking/standing Radiology: CT, Xray, MRI to rule out herniation and look for nerves ``` Treatment: Analgesics physical therapy epidural injections surgical decompression ```
65
Cauda equina syndrome
trauma to the nerves running in the dural sac ``` H and P: urinary retention change in bowel habits saddle anesthesia due to impairment of the pudendal nerve decreased rectal tone bulbocavernosus reflex impairment ``` Treatment: surgical decompression, and IV steroids to reduce risk of permanent injury Radiation in cases of neoplasm
66
Erb-Duchenne palsy: Waiter's tip
Superior trunk | MOI: hyperadduction of the arm causing widening of the humoral- glenoid gap
67
Claw hand
Ulnar nerve injury Injury to medial epicondyle of the humerus weak finger adduction poor 4th and 5th finger flexion (extended at MCP, flexed at interphalangeal finger joints)
68
wrist drop
Site of injury: radial nerve inability to extend upper fingers
69
Deltoid paralysis
axillary nerve injury associated with anterior shoulder dislocation
70
Klumke palsy
``` inferior trunk (C8 and T1) claw hand and dropped wrist ```
71
Risk factors for osteoporosis
``` low dietary calcium smoking alcohol sedentary lifestyle post- menopause decreased testosterone steroids (>3 months, add ppx bisphosphonates) ``` hyperparathyroidism hyperthyroidism Classic presentation: thin, white or Asian, post-menopausal woman Less likely to occur in obese people who bear more weight Complications: vertebral fracture colles fracture Diagnosis: DEXA scan of hip and lumbar spine Dual Energy x-ray Absorptiometry labs normal Treatment: weight-bearing exercise calcium vitamin D bisphosphonates (alendronate, etidronate, pamidronate) Raloxifene (SERM) Teriparatide (pulsatile PTH analog) daily injection for 2 years that stimulates osteoblasts to lay down new bone denosumab (RANK-L inhibitor that inhibits osteoclast activity)
72
Osteopetrosis
``` rock-like bone impaired osteoclastic activity increased risk of fractures boney compression of nerves (hearing loss, vision loss) thickening of bones in skull and spine ``` Labs: anemia increased acid phosphatase increased creatine kinase normal calcium normal phosphate normal alk phos
73
Pagent disease of bone
overactive osteoclasts and osteoblasts new bone is disorganized focal discrete lesions axial spine and long bones of legs are affected usually asymptomatic ``` May have symptoms: bone pain increased fractures bowing of tibia kyphosis narrowing of auditory foramen increased cranial diameter overgrowth of bone in skull ``` Labs: increased Alk Phos normal calcium and phosphate Treatment: bisphosphonates calcitonin- injectable SQ most cases do not require treatment
74
Osteogenesis imperfecta
``` pediatric disease type I collagen disorder brittle bones frequent fractures from minimal trauma (may resemble child abuse) blue sclerae pliable skin joint hypermobility teeth deformities deafness or hearing loss ``` Tx:bisphosphonates restrict activity surgical correction of bony misalignment
75
Gout
arthritis: sodium urate crystals that precipitate out of blood and get deposited in the joints usually, the small peripheral joints, like first MTP joint inflammatory response to these crystals causes arthritis and pain ``` Risk factors: renal disease (hyperuricemia) male sex obesity purine-rich foods- organ meat, seafood, alcohol urate underexcretion diuretics cyclosporine cancer ``` red hot painful joint, without systemic symptoms serum uric acid either normal or increased joint aspiration will show needle-shaped negatively birefringent crystals, yellow when parallel to light, an inflammatory cells blue needles perpendicular to polarized light ``` Acute Treatment: NSAIDs -indomethacin -ketorolac -ibuprofen -naproxen -celecoxib Steroids (prednisone) work safer and faster ``` Colchicine inhibits microtubules, 3rd line, use 2 low doses) SE- GI upset ``` Longterm management: decrease alcohol use decrease diuretic use avoid purine-rich foods Probenecid, inhibits uric acid resorption in the kidney ``` Allopurinol, inhibits xanthine oxidase Complications: chronic tophaceous gout
76
Pseudogout | CPPD
calcium pyrophosphate dihydrate deposited in the joints affects different joints knee or wrist MC postively birefringent rhomboid crystals yellow when perpendicular chondrocalcinosis on xray especially visible in the menisci treatment: NSAIDs, colchicine to address inflammation
77
Acute gout treatment
NSAIDs steroids colchicine NOT probenecid or steroids
78
Pseudogout treatment
NSAIDs | Colchicine
79
narrowing of the marrow cavity results in low H and H
osteopetrosis
80
55yo female who trips and sustains distal radius fracture
Colles, osteoporosis
81
How do we treat osteogenesis imperfecta in children
bisphosphonates
82
What test do we use to test for Paget disease?
Radionuclide bone scan to look for metabolic hot spots
83
Physcial exam- sIgns of radial nerve damage
wrist drop | lost thumb abduction
84
Causes of septic joint
MCC: staph a Sexually active? also consider n. gonorrhea DM, cancer, other underlying illess: gram- negative rods
85
Presentation of septic joint
sudden onset joint pain pain with any motion children: vague signs of pain, refusal to walk Labs: increased WBC count, increased ESR, increased CRP ``` Joint aspiration shows numerous WBCs with >50,000/mm^3 high % PMN decreased glucose positive cultures ``` Treatment: surgical irrigation drainage Vancomycin if staph aureus (assume MRSA with any staph infection) Ceftriaxone if n. gonorrhoeae Aminoglycosides if gram- negative bacteria
86
Joint aspirate leukocytes in | OA vs. inflammatory arthropathy vs septic joint
OA 50,000/mm^3
87
Osteomyelitis
MCC staph aureua Coagulase- negative staph Pseudomonas Salmonella MCC in SCD ``` H and P: Bone pain tenderness fever chills possible skin involvement with a draining sinus ``` Labs: increased WBC, ESR, CRP, culture, biopsy Radiology: Xrays not helpful until >10 days bone edema on MRI on bone scan, increased uptake after 72 hours tagged WBC scan Treatment: IV abx for 4-6 weeks (vancomycin assumin MRSA then alter according to culture results) I and D for abscess inside bone or surrounding tissue Complications: chronic osteomyelitis amputation
88
Lyme disease- classic presentation and clinical course Early localized disease Early disseminated disease
Early localized disease (80% of patients, usually within 1 month -erythema chronicum migrans- bull's eye rash with central clearing that expands over days to weeks +/- constitutional symptoms (fatigue, HA, myalgias, arthralgias) Early disseminated disease- weeks to months after the tick bite, may include the following: - Meningitis (lymphocytic) - Unilateral or bilateral cranial nerve palsies (esp facial nerve with b/l Bell's palsy) - Radiculopathy - Peripheral neuropathy - Carditis (AV heart block, myopericarditis) Late Lyme disease- months to years after infection onset - arthritis (esp knee) - subacute encephalitis Labs: ELISA and Western Joint aspiration if NOT helpful
89
What is the treatment for Lyme disease?
Early Lyme disease treatment options (14-21 days) - Doxycycline (preferred agent, can be dosed over only 14 days, avoid in pregnancy) - Amoxicillin - Cefuroxime Late Lyme disease (carditis, encephalitis, arthritis), usually ceftriaxone for 14-28 days
90
Treatment for RMSF
Doxycycline for about 7 days | Chloramphenicol in pregnant patients
91
Osteoarthritis, aka degenerative joint disease Chronic non-inflammatory
Affects articular cartilage -hips, knees, ankles, wrists, shoulders Can cause spinal stenosis and vertebral bodies ``` RF: advancing age family history obesity previous joint trauma ``` H and P: - joint crepitus - joint stiffness/pain that worsens with activity and weight-bearing, and is relieved by rest - no systemic symptoms - decreased range of motion - Heberden nodes (distal) - Bouchard nodes (proximal) - Typically asymmetric Labs: normal ESR
92
Neoplasms
Bony metastases BLT with a Kosher Pickle ``` Breast Lung (lytic, breaks down bone) Thyroid Kidney Prostate (blastic, builds up bone) ``` H and P: palpable bony mass fractures following minor trauma Labs: biopsy -increased alkaline, phosphatase Radiology: - xray - bone scan - MRI Treatment: - chemotherapy - bisphosphonates can help slow bone loss - radiation therapy - prophylactic fixation can be performed for an impending fracture
93
Osteosarcoma
Distal femur Proximal tibia Proximal humerus ``` Risk factors: Paget disease p53 mutation Familial retinoblastoma Radiation exposure Bone infarcts ``` History and physical: deep bone pain palpable bony mass ``` Labs increased alkaline phosphatase increased ESR increased LDH biopsy provides definitive diagnosis ``` ``` Radiology: sunburst pattern Codman triangle (periosteum pushed up by tumor) MRI and PET to determine extent Chest CT for determining metastasis ``` 90% 5yr survival rate for low grade
94
Ewing sarcoma
highly malignant diaphyseal long bone cancer seen in children ``` Bone pain tissue swelling fever, fatigue, weightloss fractures with minor trauma palpable mass ``` ``` Labs: increased WBCs decreased hemoglobin increased ESR biopsy important for making this diagnosis ``` Xray: large lesions with significant periosteal reaction (this is onion- skinning) Codmann triangle MRI to determine extent of cancer Treatment: radiation adjuvant chemotherapy radical excision Complications: 20% 5-year survival rate if metastesized
95
Osteochondroma
lower femur, upper tibia H and P: irritated soft tissue overlying mass nontender hard on palpation Xray: bony spur pointing away from the joint Surgical excision may be indicated Complications rare
96
diseases associated with pANCA
``` 1. Pauci-immune glomerulonephritis 2, Microscopic polyangiitis 3, Eosinophilic granulomatosis with polyangiitis (Churg- Strauss syndrome) 4. Ulcerative colitis 5. Primary sclerosing cholangitis ```
97
Rheumatoid arthritis
chronic inflammatory arthritis with a lot of systemic effects type 3 hypersensitivity, more common in middle- aged and elderly women Frequently associated with HLA_DR4 Which joints are involved? PIPs and MCPs This is a symmetric polyarthropathy (DIP involvement is more consistent with OA) - hypertrophy of the synovium - granulation tissue on the articular cartilage- pannus formation - active inflammation; squishy, warm, swollen, boggy, when you push on the cartilage - ulnar deviation - hypertrophy at MCPs and PIPs - sawn neck deformities - Boutonniere deformities morning stiffness improves with use (Gel phenomenon), unlike OA which gets worse with use ``` Also: Rheumatoid nodules Pleuritis Pericarditis Scleritis ```
98
Diagnostic criteria for RA
Synovitis in at least 1 joint, not better explained by another disease, plus a total score of >6/10 (Add score of categories A-D below) A. Joint involvement swelling in 2-10 large joints= 1 point 1-3 small joints (with or without large joints)= 2 points 4-10 small joints= 3 points >10 joints (at least 1 small joint)= 5 points ``` B. Serology RF (an IgG positive in 75% of RA patients) Anti-citrullinated antibody low positive RF or ACPA= 2 points high positive RF or ACPA= 3 points ``` C. Abnormal CRP or ESR= 1 point D. Duration of symptoms >6 weeks= 1 point
99
Treatment of RA
Make the diagnosis early Refer to a rheumatologist Early use of DMARDs (start using them early) DMARDs; Hydroxychloroquine Sulfasalazine Methotrexate ``` TNFalpha inhibitors Etanercept Adalimumab Golimumab Certolizumab Infliximab (check PPD first 2/2 immunosuppression) ``` Leflunomide (inhibits immune system by inhibiting proliferation of lymphocytes) Anakinra (IL1 receptor antagonist, which is anti-inflammatory) Steroids or NSAIDs are used only as adjuncts
100
SLE
``` autoimmune, systemic women age 14-45 blacks asians latinas ``` Anti-histone antibodies ``` Diagnostic criteria (4/11) Skin disorders -malar rash -discoid rash -photosensitivity -oral ulcers Inflammatory disorders -arthritis -serositis -significantly positive ANA (non-specific), very high Organ system disorders -renal disease -neurologic disorders -hematologic disoders -immunologic disorders ``` ``` Labs: positive ANA Anti-dsDNA antibodies Anti- smoth abs anti-histone abs False positive RPR and VDRL Antiphospholipid antibodies decreased serum C3 and C4 ``` ``` Treatment: avoid sun NSAIDs hydroxychloroquine steroids anticoagulation ``` Complications: Hypercoagulability increased risk of miscarriage progressive impairment of lung, heart, brain, kidney function Infections
101
Drugs associated with drug- induced lupus
``` sulfonamides hydralazine INH Procainamide Phenytoin ``` reversible with drug cessation look for antihistone antibodies
102
Lupus immunologic markers
positive ANA anti-dsDNA abs anti-Smith abs false pos RPR
103
RA immunologic markers
Rheumatoid factor ANA HLA-DR4 Anti-citrullinated protein antibody (ACPA)
104
Polymyositis and dermatomyositis immunologic markers
ANA | Anti-Jo-1 antibodies
105
ankylosing spondylitis immunologic markers
HLA-B27
106
Scleroderma immunologic markers
Anti-Scl-70
107
CREST syndrome immunologic markers
anti-centromere abs
108
Mixed connective tissue disease immunologic markers
Anti-RNP
109
Sjogren syndrome immunologic markers
Anti-Ro | Anti-La
110
Anti-histone antibodies
Drug- induced lupus
111
HLA-DR4
RA
112
Anti-Sm antibodies
SLE
113
Anti-dsDNA antibodies
SLE
114
Lupus skin findings (n=4)
malar rash discoid rash photosensitivity painless oral ulcers
115
Anti-Jo-1 antibodies
polymyositis
116
Anti-topoisomerase antibodies
scleroderma
117
Polymyositis and dermatomyositis
``` H and P symmetric, progressive, proximal muscle weakness occurs in legs first myalgias muscle atrophy (later stages) ``` Rash features: heliotropic (periorbital) red-purple rash "shawl sign" rash involving the shoulders, upper chest, back, worsened by UV light exposure Gottron's papuls Erythrodema in the malar region Mechanic's hands- roughened, cracking skin on the tips and lateral aspects of the fingers Polymyositis features: symmetric proximal muscle weakness myalgias and muscle tenderness in 25-50% of patients ``` Labs: elevated CK and LDH elevated ALT and AST ANA is positive in 80% Anti-Jo antibodies elevated serum myoglobin elevated urine myoglobin ``` DIagnose by muscle biopsy EMG shows spontaneous fibrillation ``` Treatment: high- dose corticosteroids methotrexate or azathioprine IVIG interstitial lung disease, increased risk for several malignancies ```
118
Polymyalgia rheumatica
multiple sites of muscle pain associated with temporal arteritis ``` H and P: temporal arteritis jaw claudication HA blindness or vision problems shoulder and pelvic girdle ``` PMR: pain, stiffness, different from myositis b/c it is without weakness difficulty raising arms and getting out of bed because of pain malaise unexplained weight loss fever joint swelling Labs: temporal arteritis temporal artery biopsy ESR Labs: PMR decreasd HCT increased ESR negative rheumatoid factor Radiology: - increased signal at tendon sheaths and synovial tissue outside of joints on MRI - positive emission or PET scans can show increased uptake in large vessels Treatment: low-dose corticosteroids, followed by tapered dose or corticosteroids Patient should experience significant improvement almost immediately Any patient diagnosed with PMR should immediately be worked up for temporal arteritis most commonly seen in elderly women
119
Fibromyalgia
associated with depression, anxiety, and IBS non-inflammatory, unknown etiology possible link to sleep apnea, RA, hypothyroid women age 20-50 ``` myalgias weakness without inflammation trigger points fatigue depression, sleep disturbances, dizziness, HA, mood disturbances ``` Treatment: reassurance that it's a real illness that is benign, not life- threatening, not deforming Walking, strength training, stretching daily relaxation techniques stress reduction encourage journaling and emotional writing of past traumatic experiences Appropriate sleep: address any sleep hygiene issues Address any other psychiatric disorders: depression, anxiety, PTSD Pharmacological treatment options: Amitriptyline or nortriptyline at bedtime- improvement in 25-45% of patients Acetaminophen + tramadol- 50% pain reduction Pregabalin Duloxetine (SNRI) Fluoxetine (+/- amitriptyline at bedtime) Milnacipran
120
Ankylosing spondylitis
RF: 20-40yo, M>F, Caucasians > blacks H and P: hip and lower back pain worse in morning and following inactivity pain improves over course of day limited ROM of spine Painful kyphosis relieved by bending forward +/- anterior uveitis ``` Labs: Positive HLA-B27 Increased or normal ESR Negative rheumatoid factor Negative ANA ``` Radiology: Bamboo spine on xray (encased intervertebral discs) MRI shows increased signal in the sacroiliac joints ``` Treatment: physical therapy NSAIDs Sulfasalazine Methotrexate Anti-TNF drugs ```
121
Psoriatic arthritis
develops in 10-20% of patients who have psoriasis DIP joints and spine are more commonly affected ``` H and P: asymmetric joint pain and stiffness symptoms worse in the morning, improved with activity +/- anterior uveitis joint line pain pain with stress on joints pitting of nails ``` Labs: negative rheumatoid factor negative ANA positive HLA-B27 Radiology: destructive lesions of DIP and PIP on xray "pencil in cup deformity" marrow edema on MRI ``` Treatment: NSAIDs Methotrexate Sulfasalazine Anti-TNF drugs ``` ``` PEAR Psoriatic arthritis Enteropathic arthritis (IBD) Ankylosing spondylitis Reactive arthritis (Reiter syndrome) ```
122
Limited Cutaneous systemic sclerosis: CREST Scleroderma
chronic multisystem sclerosis ``` H and P: Arthralgias, myalgias, hand swelling Raynaud phenomenon Esophageal dysmotility skin thickening ``` no wrinkles intestinal hypomotility dyspnea arrythmias or heart failure Labs: Positive Anti-SCL-70 ANA Primarily, CREST is a clinical diagnosis, but lab studies can provide support. CREST= Calcinosis cutis: subQ calcifications often in the fingers, not always present Raynaud phenomenon: cyanotic vasoconstriction, especially in the fingers Esophageal dysmotility: due to lower esophageal sphincter sclerosis leading to reflux, dysphagia Sclerodactyly: skin fibrosis, especially in the fingers, hands, and face Telangiectasias: on the lip, hand, or face; not always present Labs: anti-Scl-70 anti-RNA anti-U1-RNP anti-centromere (lab work can support the diagnosis but cannot rule out scleroderma) ``` Treatment: supportive care ACE inhibitors Dihydropyridine CCBs Avoid caffeine, nicotine, decongestants Methotrexate Corticosteroids ``` Complications: Pulmonary fibrosis Heart failure Acute renal failure caused by malignant hypertension
123
Mixed connective tissue disease
A mix of symptoms and feature can progress + anti-ribonucleoprotein (RNP)
124
Sjogren syndrome
-dry eyes, dry mouth (sicca syndrome) -enlarged parotid glands purpura of the legs -peripheral neuropathy -possible symmetric arthritis with other autoimmune conditions Positive anti-Ro antibodies Positive anti-La antibodies lymphocytic infiltration of exocrine glands Treatment: supportive care corticosteroids
125
What labs do you order when you suspect dermatomyositis?
``` CK aldolase AST, ALT LDH ANA Anti-Jo 1 BMP CBC ```