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128 Cards in this Set

  • Front
  • Back
Inflammatory monoarthritis that often forms sinus tracts
TB arthritis
Infectious inflammatory polyarthritis with a false (+)ve RF
Hepatitis C
Arthritis location classically associated with sarcoidosis
Ankle Arthritis
DDx of a joint so painful,the patient will not let you move it
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
Bilateral shoulder and hip stiffness; worse in the morning and better later in the day. "Rolls out of bed".
Polymyalgia Rheumatica
-- Periarticular tenosynovium; NOT a myopathy
-- Start Prednisone 15 mg daily
B/L Shoulder weakness + Increased ESR + Increased CPK
Polymyositis
HA + visual changes + Jaw Claudication + shoulder/hip stiffness
GCA -- high dose prednisone
(+)ve Empty Can Sign
Supraspinatus Tendonitis --- most commonly involved
Gout drug associated with neuromyopathy and elevated CPK
Colchicine
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?
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
Antibody that predicts interstitial lung disease in patients with inflammatory myopathies
Positive Anti-Jo-1 Antibody predicts interstitial lung disease in patients with polymyositis/dermatomyositis.
Inflammatory myopathy that is T-cell mediated with endomysial inflammation
Polymyositis (P-E-T)
Inflammatory myopathy that is B-cell mediated with perivascular, perimysial inflammation
Dermatomyositis (D-B)
Mechanic's Hands and Dilated nailbed capillaries
Dermatomyositis
Calcinosis cutis (calcification of muscle)
Dermatomyositis
Association of malignancy with inflammatory myopathies
Malignancy associated with Dermatomyositis NOT Polymyositis

LOOK FOR CANCER IN DERMATOMYOSITIS -- AGGRESSIVE SCREENING!
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
Most common cause of scleritis (Deep boring pain of the eye)
Rheumatoid Arthritis
Miner with Pulmonary nodules/Pneumoconiosis + RA
Caplan syndrome -- associated with silica exposure
Leukopenia + Splenomegaly + RA

Increased infections, leg ulcers
Felty Syndrome
Side effects of Hydroxychloroquine
Retinopathy

Myopathy

Rash/diarrhea
Side effects of sulfasalazine
Serious - Agranulocytosis

Mild - Rash, increased LAEs, Azospermia
Side effects of methotrexate
Serious - cirrhosis, leukopenia, anemia, pnumonitis, reversible lymphoma

Mild - stomatitis, icnreased LAEs, Alopecia
Side effects of TNF-inhibitors
Serious - TB reactivation, fungal infxns, MS-like dz, HBV reactivation (NOT HCV), infection
Dactylitis (sausage digits)
Psoriasis

Reason: psoriasis lvoes inflammation of tendon insterts
Sudden onset of Psoriasis as an adult; Next step?
Check HIV status
Arthritis associated with keroterma blennorrhagicum and circinate balanitis
Reactive Arthritis
Gull Wing appearance of DIPs
OA
Which part of the knee does OA affect (Medial Vs. Lateral)
Medial
Swelling along the distal radius and pain with ulnar deviation of the wrist -- pain with extending thumb.

(+) finkelstein's test
DeQuervain's Tenosynovitis
Patient with Raynaud's finding --- What is the best way to predict if the patient will develop a connective tissue disease?
Check Nailfold Capillaroscopy -- if nailfold capillaries noted, then patient is at increased risk of CTD.
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
Adult Still's Disease
(+)ve anatomical snuff box
Check for scaphoid fx -- CT/MR if Hand X-ray negative
Important complications of Ankylosing Spondylitis
- 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
Endplate destruction
Think Osteomyelitis -- check MRI
Most specific sign for meniscal tear
McMurray Test

most sensitive -- joint line tenderness
Pain with getting up from a sitting position

Going down stairs is worse
Patellofemoral syndrome

crescent sign, patient has a ruptured baker's cyst

Associated with psedothrombophlebitis
Tx of gout if kidney injury
Intraarticular steroids

Note -- do not start allopurinol in the setting of an acute gout flare; wait after the flare
Medications that should be avoided in gout
Thiazides
Niacin
Calcinurin inhibitors (Tacrolimus)
LD ASA
Laxatives in excess
Medications that help gout patients
Vit C
Losartan
Statins
Dairy
Low purine diet
Avoid EtOH (Wine ok, beer bad)
Reasons to use hypouricemic tx
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
Side effect of allopurinol
Rash, Hypersensitivity Syndrome
Cannot plantar flex while squeezing calf
Sing of achilles tendon rupture -- Thompson's Test
Elderly patient with anemia, fatigue. ESR elevated, but CRP normal.
Check SPEP/UPEP

Associated with MM
Patient with Raynaud's + Arthritis + Dysphagia + small red dots on her face and hands appearing over the last 6 months; Next step?
Check anti-centromere antibodies for Limited Scleroderma (CREST)
Anti-SSA/SSB
Sjogren's
Anti-dsDNA
Specific for SLE
Anti-Scl-70
Diffuse Scleroderma
A positive ANA of 1:40 or 1:80
Clinically insignificant --> Ignore
A child born to a mom with SLE has the above rash --- what antibody did the mom have?
A child born to a mom with SLE has the above rash --- what antibody did the mom have?
Anti-SSA (RO) antibodiy

Associated with Neonatal Lupus in child and congenital heart block
Can use this antibody to follow the course of SLE
DsDNA
Complement deficiency in SLE
C2*, C4
Is discoid lupus associated with SLE?
Not really -- usually an isolated dz w/o systemic findings

Only 5-10% with isolated discoid lupus will progress to SLE
Arthopathy associated with SLE
RA-like --> Jacoud's Arthropathy

Hypermobility of joint
Rx of lupus nephritis
Cyclophosphamide
Important complications to know associated with SLE
(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
Drugs associated with positive ANCA
Minocycline

Propylthiouracil -- Most common drug to cause (+ve) ANCA
Anti-mitochondrial Antibody
Primary Biliary Cirrhosis (PBC)
Anti-smooth Muscle Antibody
Autoimmune Hepatitis
Anti-LKM
Autoimmune Hepatitis
Anti-thyroglobulin Antibody
Hashimotos
Anti-microsomal Antibodies
Hashimoto's

Anti-TPO
Unequal BP

Carotidynia

UE Claudication

Stroke in a young woman

Renovascular HTN

Increased ESR/CRP
Takayasu's

Do an angiogram/MRA
Polyarteritis Nodosa spares what organ
Lungs
Cauliflower ear
Relapsing Polychondritis
DDx of Saddle Nose Deformity
GPA
Relapsing polycondritis
Congenital Syphilis
Trauma
Cocaine use
Staining for which class of antibody is useful for dx of Henoch-Schonlein purpura
IgA
Most common cause of leukocytoclastic vasculitis
Remove offending drug (antibiotics, anti-sz meds, allopurinol)
Watermelon stomach (GAVE)
Associated with Diffuse Scleroderma -- causes GIB
Scleroderma REnal Crisis Tx
ACE-I (Captropril)
Indentation along superficial veins (Groove Sign) + Eosinophilia + onset following vigorous exercise
Eosinophilic Fasciitis

- Associated with lymphomas
Leg pain with walking down hill; relief of pain when leaning forward while walking or standing erect.
Neurogenic Claudication
Discomfort with abduction of leg + Groin Pain
Hip OA
Point tenderness over the medial knee and negative valgus stress maneuver
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
Complications of Dermatomyositis
- 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
Patient with controlled SLE desires to be pregnant; next step?
- 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
Tx of choice for symptomatic acute vertebral fractures
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.
Drug-Induced Vasculitis criteria
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)
Dx Criteria for Sjogren's Syndrome
-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)
Antisynthetase antibodies
classically, Anti-Jo-1 -- for myositis
Anti-topoisomerase Ab = ?
SCL-70

Scleroderma associated with Anti-Scl70 (Antitopoisomerase), Anticentromere, and anti-RNA polymerase II Abs
Feared complication of limited vs. diffuse scleroderma
Pulmonary HTN --> Limited SS

Pulmonary Fibrosis --> Diffuse SS
Indicated in individuals at high risk of fractuer and those failing other therapeutic agents
Teriparatide (recomobinant form of parathyroid hormone)
Stomatitis in patient receiving MTX
GIVE FOLATE ACID
2 diseases to watch out for when giving TNF-inhibitors
TB reactivation

HBV reactivation (NOT HCV)
Recurrent Abdominal/Testicular Pain + HBV history + Mononeuritis Multiplex
Polyarteritis Nodosa
Tx of respiratory impairment in Ankylosing Spondylitis
Noninvasive Positive Pressure Ventilation
Cytoplasmic Vacuolization on muscle biopsy + Proximal Muscle wekness + Neuropathy + Elevated CPK
Colchicine Toxicity -- D/C Colchicine
Intermittent painless swelling of partoid glands in long-standing Sjogren Patient -- what is the likely dx?
NHL - B-cell type

RFs - Anti-RO/La, RF, Cryoglobulinemia, Hypocomplimentemia, and lymphocytopenia
Confirming dx test for a patient who presents with lower extremity paplpable purpura, nonspecifgic abdominal symptoms, renal disease, arthritis/arthralgias with recent infection
Skin Biopsy shows IgA deposition --- Henoch Schonlein Purpura
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
Complex Regional Pain Syndrome
Elderly patient who reports stiffness with >50% reduction in both passive and active ROM
Adhesive Capsulitis

NOTE: PMR is associated with active >>> passive decreased ROM
Knee swelling after parathyroidectomy
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
Ankylosing Spondylitis unrelieved by NSAIDs, PT, and local measures; next step?
TNF-inhibitor (Adalimumab)
OA in an RA distribution
Hemochromatosis
Prognostic Factors for Erosive RA
(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
Neutropenia + lymphocytosis + RA
Large Granular Lymphocyte Syndrome
Decreased C4 + Purpura
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!
Punch purpura + Cardiomyopathy + Proteinuria
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)
Hypocomplimentemia Disorders (Decreased c3 and c4)
"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
Older woman with trauma to shoulder -- develops a destructive inflammatory arthritis (Milwaukee Shoulder) with effusion - what crystals are associated?
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.
What is the difference between pseudogout and CPPD?
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.
Patient with Carpal Tunnel Syndrome and Fatigue and >60 min of morning stiffness
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.
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
Drug-Induced Lupus
Subacute Cutaneous Lupus Erythematous (SCLE)
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.
Can be effective in the management of both peripheral arthritis and skin manifestations that occur in patients with psoriatic arthritis.
Methotrexate
Considered first-line therapy for patients with axial spondyloarthritis.
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.
Initial treatment of patients with polyarteritis nodosa who also have active hepatitis B virus infection
A limited course of corticosteroids in conjunction with antiviral therapy.
If temporal artery biopsy results are negative for giant cell arteritis (GCA) in a patient with cranial symptoms, what's the next step?
A biopsy of the contralateral temporal artery is then indicated to diagnose GCA
Most common disease-related cause of death in patients with mixed connective tissue disease.
Pulmonary arterial HTN
Gold standard disease-modifying antirheumatic drug therapy for rheumatoid arthritis and is central to most treatments for the disease.
Methotrexate
A category of cutaneous sclerosis that involves only the skin in the absence of other systemic manifestations of systemic sclerosis.
Morphea
Periodic monitoring for changes in _________ is indicated for patients receiving tocilizumab.
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.
Standard first-line treatment for patients with uncomplicated dermatomyositis.
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.
Indicated for patients diagnosed with or suspected of having relapsing polychondritis to evaluate for large upper airway involvement.
PFTs with flow volume loops
Indicated for acute digital ischemia in the setting of limited cutaneous systemic sclerosis.
IV Epoprostenol
Tx for patients with frequently recurring gout attacks.
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.
Tx of patients with Churg-Strauss syndrome who have cardiac, GI, renal or CNS involvement
High dose steroid + Cyclophosphamide
Warranted in patients with Raynaud phenomenon in whom cold avoidance does not provide sufficient relief.
Dihydropyridine CCB (e.g. Amlodipine)
Tx of CNS lupus
Methylprednisolone + Cyclophosphamide
1st line tx for psoriatic arthritis
Methotrexate (as long as no e/o liver injury or alcoholism)
Most common reason for greasy diarrhea in a patient with limited or diffuse systemic sclerosis?
Bacterial Overgrowth
Helpful diagnostic test in patients with persistent proximal muscle myopathy (CKemia)?
MRI of the thighs to assess of inflammation is present.
In patients with dermatomyositis on long term steroid tx, what drug can be added to further taper the dose of steroids?
Methotrexate
Patient on a TNF-alpha inhibitor develops cancer; next step?
D/c TNF-alpha inhibitor
Autoimmune inflammatory disorder characterized by nonsyphilitic keratitis and audiovestibular dysfunction that results in progressive hearing loss.
Cogan Syndrome
Important points regarding Reactive Arthritis
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.