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128 Cards in this Set
- Front
- Back
Inflammatory monoarthritis that often forms sinus tracts
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TB arthritis
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Infectious inflammatory polyarthritis with a false (+)ve RF
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Hepatitis C
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Arthritis location classically associated with sarcoidosis
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Ankle Arthritis
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DDx of a joint so painful,the patient will not let you move it
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Think "BBC"
(1) Bugs: - NG bacterial arthritis - Gonococcal arthritis (2) Blood in joint - ACL tear/Meniscal tear - Hemophilia - Anticoag use - Intra-articular fx (3) Crystals - Urate gout - CPPD |
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Bilateral shoulder and hip stiffness; worse in the morning and better later in the day. "Rolls out of bed".
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Polymyalgia Rheumatica
-- Periarticular tenosynovium; NOT a myopathy -- Start Prednisone 15 mg daily |
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B/L Shoulder weakness + Increased ESR + Increased CPK
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Polymyositis
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HA + visual changes + Jaw Claudication + shoulder/hip stiffness
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GCA -- high dose prednisone
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(+)ve Empty Can Sign
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Supraspinatus Tendonitis --- most commonly involved
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Gout drug associated with neuromyopathy and elevated CPK
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Colchicine
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Patient with polymyositis flare treated with steroids --- steroids tapered and weakness relapses but CPK is lower than prior to when the pt had the initial flare. What is then next step?
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Taper the steroids more rapidly --> the patient has steroid induced myopathy
Steroids have a direct catabolic affect on muscle LE>UE; weakness then atrohy develops CPK and EMG will be normal Bx will show atrphy of the type IIb fibers wtihout inflammation After safe rapid taper, improvement in 3-4 weeks |
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Antibody that predicts interstitial lung disease in patients with inflammatory myopathies
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Positive Anti-Jo-1 Antibody predicts interstitial lung disease in patients with polymyositis/dermatomyositis.
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Inflammatory myopathy that is T-cell mediated with endomysial inflammation
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Polymyositis (P-E-T)
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Inflammatory myopathy that is B-cell mediated with perivascular, perimysial inflammation
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Dermatomyositis (D-B)
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Mechanic's Hands and Dilated nailbed capillaries
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Dermatomyositis
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Calcinosis cutis (calcification of muscle)
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Dermatomyositis
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Association of malignancy with inflammatory myopathies
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Malignancy associated with Dermatomyositis NOT Polymyositis
LOOK FOR CANCER IN DERMATOMYOSITIS -- AGGRESSIVE SCREENING! |
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Men>Women; Age >50
Distal>Prox Weakness and atrophy Asymmetiric atrophy of florearm flexors, intrinsic hand muscle, quads "Tear Drop Sign" -- can't make an "o" with hands Esophageal problems Normal to low CPK Unresponsive to steroids |
Inclusion Body Myositis
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Most common cause of scleritis (Deep boring pain of the eye)
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Rheumatoid Arthritis
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Miner with Pulmonary nodules/Pneumoconiosis + RA
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Caplan syndrome -- associated with silica exposure
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Leukopenia + Splenomegaly + RA
Increased infections, leg ulcers |
Felty Syndrome
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Side effects of Hydroxychloroquine
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Retinopathy
Myopathy Rash/diarrhea |
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Side effects of sulfasalazine
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Serious - Agranulocytosis
Mild - Rash, increased LAEs, Azospermia |
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Side effects of methotrexate
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Serious - cirrhosis, leukopenia, anemia, pnumonitis, reversible lymphoma
Mild - stomatitis, icnreased LAEs, Alopecia |
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Side effects of TNF-inhibitors
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Serious - TB reactivation, fungal infxns, MS-like dz, HBV reactivation (NOT HCV), infection
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Dactylitis (sausage digits)
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Psoriasis
Reason: psoriasis lvoes inflammation of tendon insterts |
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Sudden onset of Psoriasis as an adult; Next step?
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Check HIV status
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Arthritis associated with keroterma blennorrhagicum and circinate balanitis
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Reactive Arthritis
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Gull Wing appearance of DIPs
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OA
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Which part of the knee does OA affect (Medial Vs. Lateral)
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Medial
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Swelling along the distal radius and pain with ulnar deviation of the wrist -- pain with extending thumb.
(+) finkelstein's test |
DeQuervain's Tenosynovitis
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Patient with Raynaud's finding --- What is the best way to predict if the patient will develop a connective tissue disease?
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Check Nailfold Capillaroscopy -- if nailfold capillaries noted, then patient is at increased risk of CTD.
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Quotidian fever (High spiking fever that comes down), intermittent salmon rash on chest and extremities with Koebner phenomenon, Arthritis, Lymphadenopathy, Neutrophilia (WBC in the 20s), Anemia, increased LAEs, Hyperferritenemia
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Adult Still's Disease
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(+)ve anatomical snuff box
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Check for scaphoid fx -- CT/MR if Hand X-ray negative
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Important complications of Ankylosing Spondylitis
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- Vertebral dix space fx following mild trauma (classically c5-7)
- Bilateral upper lobe fibrosis; may cavitate; can be colonized by aspergillosis and form mycetomas - Restrictive pulmonary disease - Uveitis that is vision threatening - Cauda Equina Syndrome - Amyloidosis - Aortic valve incompetence - Mortatily increased after 20 yrs of disease --> increased heart dz d/t chronic inflammation |
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Endplate destruction
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Think Osteomyelitis -- check MRI
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Most specific sign for meniscal tear
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McMurray Test
most sensitive -- joint line tenderness |
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Pain with getting up from a sitting position
Going down stairs is worse |
Patellofemoral syndrome
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crescent sign, patient has a ruptured baker's cyst
Associated with psedothrombophlebitis |
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Tx of gout if kidney injury
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Intraarticular steroids
Note -- do not start allopurinol in the setting of an acute gout flare; wait after the flare |
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Medications that should be avoided in gout
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Thiazides
Niacin Calcinurin inhibitors (Tacrolimus) LD ASA Laxatives in excess |
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Medications that help gout patients
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Vit C
Losartan Statins Dairy Low purine diet Avoid EtOH (Wine ok, beer bad) |
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Reasons to use hypouricemic tx
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3 or more gouty attacks/year
Tophi or joint damage present Uric acid >11 in Female; >13 in Male Goal is <6; <5 if tophi present |
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Side effect of allopurinol
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Rash, Hypersensitivity Syndrome
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Cannot plantar flex while squeezing calf
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Sing of achilles tendon rupture -- Thompson's Test
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Elderly patient with anemia, fatigue. ESR elevated, but CRP normal.
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Check SPEP/UPEP
Associated with MM |
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Patient with Raynaud's + Arthritis + Dysphagia + small red dots on her face and hands appearing over the last 6 months; Next step?
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Check anti-centromere antibodies for Limited Scleroderma (CREST)
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Anti-SSA/SSB
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Sjogren's
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Anti-dsDNA
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Specific for SLE
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Anti-Scl-70
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Diffuse Scleroderma
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A positive ANA of 1:40 or 1:80
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Clinically insignificant --> Ignore
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A child born to a mom with SLE has the above rash --- what antibody did the mom have?
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Anti-SSA (RO) antibodiy
Associated with Neonatal Lupus in child and congenital heart block |
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Can use this antibody to follow the course of SLE
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DsDNA
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Complement deficiency in SLE
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C2*, C4
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Is discoid lupus associated with SLE?
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Not really -- usually an isolated dz w/o systemic findings
Only 5-10% with isolated discoid lupus will progress to SLE |
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Arthopathy associated with SLE
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RA-like --> Jacoud's Arthropathy
Hypermobility of joint |
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Rx of lupus nephritis
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Cyclophosphamide
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Important complications to know associated with SLE
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(1) INFECTIONS
- Functional Asplenia (encapsulated organisms) - Immunocompromising infections (PCP, aspergillosis, Crypto) (2) Osteonecrosis (3) CAD, Libman-Sacks endocarditis, vasculitidies (4) Osteoporosis (5) Ovarian failure from cyclophosphamide use |
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Drugs associated with positive ANCA
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Minocycline
Propylthiouracil -- Most common drug to cause (+ve) ANCA |
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Anti-mitochondrial Antibody
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Primary Biliary Cirrhosis (PBC)
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Anti-smooth Muscle Antibody
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Autoimmune Hepatitis
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Anti-LKM
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Autoimmune Hepatitis
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Anti-thyroglobulin Antibody
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Hashimotos
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Anti-microsomal Antibodies
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Hashimoto's
Anti-TPO |
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Unequal BP
Carotidynia UE Claudication Stroke in a young woman Renovascular HTN Increased ESR/CRP |
Takayasu's
Do an angiogram/MRA |
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Polyarteritis Nodosa spares what organ
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Lungs
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Cauliflower ear
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Relapsing Polychondritis
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DDx of Saddle Nose Deformity
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GPA
Relapsing polycondritis Congenital Syphilis Trauma Cocaine use |
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Staining for which class of antibody is useful for dx of Henoch-Schonlein purpura
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IgA
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Most common cause of leukocytoclastic vasculitis
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Remove offending drug (antibiotics, anti-sz meds, allopurinol)
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Watermelon stomach (GAVE)
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Associated with Diffuse Scleroderma -- causes GIB
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Scleroderma REnal Crisis Tx
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ACE-I (Captropril)
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Indentation along superficial veins (Groove Sign) + Eosinophilia + onset following vigorous exercise
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Eosinophilic Fasciitis
- Associated with lymphomas |
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Leg pain with walking down hill; relief of pain when leaning forward while walking or standing erect.
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Neurogenic Claudication
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Discomfort with abduction of leg + Groin Pain
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Hip OA
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Point tenderness over the medial knee and negative valgus stress maneuver
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Anserine bursitis
- place a pillow b/w kneeds at night, avoid leg crossing, limit repetitive knee bending, and use ice to reduce pain. - NSAIDs are ok |
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Complications of Dermatomyositis
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- Interstitial lung disease
- Malignancy (lung, ovarian, etc.) - Esophageal disease (i.e. weakness of proximal muscles, oropharyngeal muscles and striated muscles in the upper 1/3 of the esophagus) --- Dysphagia, nasal regurgitation, and/or aspiration (ESPECIALLY IN OLDER PATIENTS) - Myocarditis |
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Patient with controlled SLE desires to be pregnant; next step?
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- Check anti-phospholipid antibodies (for thrombotic risk/pregnancy loss risk), Anti-RO/SSA Ab (for possibility of neonatal lupus/heart block)
**Pregnant women with APL are usually tx with ASA and/or LMWH, depending on prior hx of fetal loss or pregnancy complications **Note: Hydroxychloroquine is safe in pregnancy |
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Tx of choice for symptomatic acute vertebral fractures
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Symptomatic vertebral compression fractures are managed acutely by NSAIDs, Tylenol, and Sometimes opioids. When this tx fails, intranasal calcitonin for 2-4 weeks can provide symptomatic relief. Long term, bisphosphonates should be give but this will not provide short term relief.
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Drug-Induced Vasculitis criteria
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Age >16
Temporal relationship b/w offending drug use and symptom onset Palpable purpura Maculopapular rash Skin bx showing leukocytoclastic vasculitis (neutrophils around an arteriole or venule) |
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Dx Criteria for Sjogren's Syndrome
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-Ocular symptoms (dry eyes/decreased tears)
-Oral symptoms (dry mouth, swollen salivary glands) -Positive ocular signs (Schirmer Test) -Salivary gland biopsy (**lower lip bx diagnostic**) with focal lymphocytic sialoadenitis -Salivary gland involvement (e.g. decreased salivary flow, delayed uptate on salivary scintigraphy) -Autoantibodies to RO/La (SSA/SSB) |
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Antisynthetase antibodies
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classically, Anti-Jo-1 -- for myositis
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Anti-topoisomerase Ab = ?
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SCL-70
Scleroderma associated with Anti-Scl70 (Antitopoisomerase), Anticentromere, and anti-RNA polymerase II Abs |
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Feared complication of limited vs. diffuse scleroderma
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Pulmonary HTN --> Limited SS
Pulmonary Fibrosis --> Diffuse SS |
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Indicated in individuals at high risk of fractuer and those failing other therapeutic agents
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Teriparatide (recomobinant form of parathyroid hormone)
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Stomatitis in patient receiving MTX
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GIVE FOLATE ACID
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2 diseases to watch out for when giving TNF-inhibitors
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TB reactivation
HBV reactivation (NOT HCV) |
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Recurrent Abdominal/Testicular Pain + HBV history + Mononeuritis Multiplex
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Polyarteritis Nodosa
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Tx of respiratory impairment in Ankylosing Spondylitis
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Noninvasive Positive Pressure Ventilation
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Cytoplasmic Vacuolization on muscle biopsy + Proximal Muscle wekness + Neuropathy + Elevated CPK
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Colchicine Toxicity -- D/C Colchicine
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Intermittent painless swelling of partoid glands in long-standing Sjogren Patient -- what is the likely dx?
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NHL - B-cell type
RFs - Anti-RO/La, RF, Cryoglobulinemia, Hypocomplimentemia, and lymphocytopenia |
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Confirming dx test for a patient who presents with lower extremity paplpable purpura, nonspecifgic abdominal symptoms, renal disease, arthritis/arthralgias with recent infection
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Skin Biopsy shows IgA deposition --- Henoch Schonlein Purpura
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Presents after an injury with throbbing pain, paresthesias, skin temp changes, and local edema. Dx is suggested clinically by symptoms and abrupt relieft with a local anesthetic blcok
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Complex Regional Pain Syndrome
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Elderly patient who reports stiffness with >50% reduction in both passive and active ROM
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Adhesive Capsulitis
NOTE: PMR is associated with active >>> passive decreased ROM |
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Knee swelling after parathyroidectomy
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Likely CPPD (Pseudogout)
Parathyroidectomy can precipitate a pseudogout attack during the post-operative period. this is due to an abrupt drop in serum calcium levels, which in tern stimulates crystal shedding into the synovial fluid |
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Ankylosing Spondylitis unrelieved by NSAIDs, PT, and local measures; next step?
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TNF-inhibitor (Adalimumab)
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OA in an RA distribution
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Hemochromatosis
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Prognostic Factors for Erosive RA
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(1) (+)ve anti-CCP and RF
(2) Early development of multiple joint inflammation (3) Radiographic erosions (4) Severe functional limitations (5) Lower economic status and less education (6) Elevated ESR/CRP (7) Persistent joint inflammation >12 weeks |
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Neutropenia + lymphocytosis + RA
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Large Granular Lymphocyte Syndrome
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Decreased C4 + Purpura
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Check HCV RNA (i.e. (+)ve HCV RNA but Negative Anitbodies) --- THINK MIXED (TYPE II) CRYOGLOBULINEMIA
If HCV Ab (+) and RNA (-), think of another dx! |
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Punch purpura + Cardiomyopathy + Proteinuria
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Think Amyloidosis -- do fat pad bx (apple green birefringence on congo red stain)
Check SIED (not SPEP or UPEP) and free light chains (Ig light chain) in regards to protienuria for AL (most common) |
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Hypocomplimentemia Disorders (Decreased c3 and c4)
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"SCIMP" -- SLE + Cryoglobulinemia + Inf Endocarditis + MPGN + PSGN
Decreased C3: PSGN, MPGN, Infective Endocarditis Decreased C3/C4: SLE, Cryoglobulinemia **NOTE: IgA and HSP have normal complements |
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Older woman with trauma to shoulder -- develops a destructive inflammatory arthritis (Milwaukee Shoulder) with effusion - what crystals are associated?
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Basic Calcium Phosphate Crystals - BCP crystals cannot be seen under polarized light microscopy but can be visualized as aggregates after alizarin red staining of synovial fluid (although not done routinely), which can confirm the clinical diagnosis.
Basic calcium phosphate crystals are commonly associated with chronic and highly destructive inflammatory arthritis such as Milwaukee shoulder. |
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What is the difference between pseudogout and CPPD?
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Pseudogout is an acute inflammatory arthritis caused by CPP crystals in the joint. Although this patient has CPP deposition, there is no evidence of a current or prior acute inflammatory arthritis. This patient's 2-year history of joint pain is not consistent with acute pseudogout.
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Patient with Carpal Tunnel Syndrome and Fatigue and >60 min of morning stiffness
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Carpal tunnel syndrome is occasionally the presenting symptom of rheumatoid arthritis.
Overuse injury has not been convincingly shown to play a causative role in the pathogenesis of this neuropathy. |
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New-onset fever, arthralgia, myalgia, nonblanching purpuric rash, pleuritis, pancytopenia, and proteinuria with active urine sediment in patient with RA being treated with TNF-Inhibitor
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Drug-Induced Lupus
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Subacute Cutaneous Lupus Erythematous (SCLE)
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The annular form of SCLE is characterized by scaly erythematous circular plaques with central hypopigmentation; the less common papulosquamous variant resembles psoriasis. These rashes most commonly involve the neck, trunk, and extensor surfaces of the arms. They can be chronic and recurrent but do not scar. SCLE may be associated with medications (hydrochlorothiazide, calcium channel blockers, ACE inhibitors, and terbinafine). SCLE occurs in up to 10% of patients with systemic lupus erythematosus (SLE), usually with some of the less serious SLE manifestations (arthritis, serositis), and is associated with anti-Ro/SSA and anti-La/SSB antibodies. This condition also manifests as its own entity; up to 50% of patients with SCLE do not develop systemic manifestations of lupus.
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Can be effective in the management of both peripheral arthritis and skin manifestations that occur in patients with psoriatic arthritis.
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Methotrexate
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Considered first-line therapy for patients with axial spondyloarthritis.
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NSAIDs
Tumor necrosis factor (TNF)-α inhibitors such as etanercept are used to treat both peripheral and axial involvement that occur in spondyloarthritis. However, because of cost and long-term safety concerns, these agents currently are not recommended as first-line therapy. If NSAIDs are insufficient, poorly tolerated, or contraindicated, TNF-α inhibitors are then advised. |
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Initial treatment of patients with polyarteritis nodosa who also have active hepatitis B virus infection
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A limited course of corticosteroids in conjunction with antiviral therapy.
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If temporal artery biopsy results are negative for giant cell arteritis (GCA) in a patient with cranial symptoms, what's the next step?
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A biopsy of the contralateral temporal artery is then indicated to diagnose GCA
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Most common disease-related cause of death in patients with mixed connective tissue disease.
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Pulmonary arterial HTN
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Gold standard disease-modifying antirheumatic drug therapy for rheumatoid arthritis and is central to most treatments for the disease.
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Methotrexate
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A category of cutaneous sclerosis that involves only the skin in the absence of other systemic manifestations of systemic sclerosis.
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Morphea
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Periodic monitoring for changes in _________ is indicated for patients receiving tocilizumab.
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Lipid Status
Tocilizumab is FDA approved to treat patients with rheumatoid arthritis who have experienced an inadequate response to tumor necrosis factor α inhibitors. This biologic disease-modifying antirheumatic drug is associated with leukopenia, thrombocytopenia, and elevated serum aminotransferase levels. Tocilizumab also is associated with increases in serum cholesterol levels, a concern given the increased risk for premature cardiovascular disease associated with rheumatoid arthritis. Periodic monitoring for changes in lipid status is therefore indicated for patients receiving tocilizumab, particularly for patients with additional risk factors for coronary artery disease, as noted in this patient who has a family history of the disease. |
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Standard first-line treatment for patients with uncomplicated dermatomyositis.
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Prednisone
Immunosuppressive therapy such as azathioprine or methotrexate in conjunction with corticosteroids is an important and frequently utilized treatment option for steroid-resistant disease or as steroid-sparing therapy and is often started concurrently with prednisone for severe disease or for those in poor prognosis groups, including patients with extramuscular manifestations of cardiovascular or pulmonary involvement. Intravenous immune globulin is reserved for patients who require additional therapy in conjunction with corticosteroids or for those who have a contraindication to the use of corticosteroids or other immunosuppressive therapies. |
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Indicated for patients diagnosed with or suspected of having relapsing polychondritis to evaluate for large upper airway involvement.
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PFTs with flow volume loops
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Indicated for acute digital ischemia in the setting of limited cutaneous systemic sclerosis.
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IV Epoprostenol
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Tx for patients with frequently recurring gout attacks.
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Colchicine and Allopurinol
Gout is associated with hyperuricemia, and patients with recurrent episodes (≥2 attacks in 1 year) require urate-lowering therapy to prevent both future attacks and occult urate deposition. However, the addition of urate-lowering therapy transiently increases the risk for acute gout attacks for at least 3 to 6 months; accordingly, prophylaxis with an anti-inflammatory agent such as colchicine, at least during that period, is indicated concurrent with urate-lowering therapy. |
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Tx of patients with Churg-Strauss syndrome who have cardiac, GI, renal or CNS involvement
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High dose steroid + Cyclophosphamide
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Warranted in patients with Raynaud phenomenon in whom cold avoidance does not provide sufficient relief.
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Dihydropyridine CCB (e.g. Amlodipine)
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Tx of CNS lupus
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Methylprednisolone + Cyclophosphamide
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1st line tx for psoriatic arthritis
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Methotrexate (as long as no e/o liver injury or alcoholism)
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Most common reason for greasy diarrhea in a patient with limited or diffuse systemic sclerosis?
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Bacterial Overgrowth
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Helpful diagnostic test in patients with persistent proximal muscle myopathy (CKemia)?
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MRI of the thighs to assess of inflammation is present.
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In patients with dermatomyositis on long term steroid tx, what drug can be added to further taper the dose of steroids?
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Methotrexate
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Patient on a TNF-alpha inhibitor develops cancer; next step?
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D/c TNF-alpha inhibitor
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Autoimmune inflammatory disorder characterized by nonsyphilitic keratitis and audiovestibular dysfunction that results in progressive hearing loss.
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Cogan Syndrome
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Important points regarding Reactive Arthritis
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presence of inflammatory arthritis that manifests within 2 months of an episode of bacterial gastroenteritis or nongonococcal urethritis or cervicitis in a genetically predisposed patient. This patient’s history of conjunctivitis preceding her musculoskeletal symptoms is also consistent with this condition. Historically, what is now called reactive arthritis was previously called Reiter syndrome, which referred to the co-incidence of arthritis, conjunctivitis, and urethritis (or cervicitis). However, only one third of affected patients have all three symptoms. Reactive arthritis usually has an asymmetric oligoarticular pattern and involves the lower extremities; inflammatory back pain also may be present. Reactive arthritis also may be associated with enthesitis, which commonly manifests as Achilles tendinitis (as seen in this patient), plantar fasciitis, and spondylitis. Reactive arthritis also is associated with numerous cutaneous manifestations, including keratoderma blenorrhagicum, oral ulcerations, and circinate balanitis.
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