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447 Cards in this Set

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What is the most common cause of prosthetic joint septic arthritis?
Staph aureus (after staph, 2nd MCC is strep in non-gonococcal arthritsi)
How does septic arthritis present?
Acute onset of painful, swollen joint with limited ROM and fever. But, crystal-induced arthritis can present similarly, so need synovial fluid for dx. WBC of 10,000-50,000 can be found in crystal-induced arthritis, whereas 50,000-150,000 stromgly suggestive of septic arthritis. Also, fever higher in septic.
What is the MCC of septic arthritis in young, sexually active individuals? How present?
Neisseria gonorrhea. Purulent arthritis affecting one or more joints or as polyarthritis assoc with tenosynovitis and skin rash
What is reactive arthritis often linked to and what is the triad?
GU infection with Chlamydia. Triad of arthritis, conjunctivitis, urethritis
What does Borrelia burgdorferi cause?
Lyme disease. Can cause arthritis, facial palsy, cardiac conduction abmoralities
What joint problems can TB and Blastomycosis cause?
Both can cause arhtirits, but far less common than bacterial arthritis and are less virulent and acute and with lower synovial WBC count than bacterial arthritis
Who does Salmonella and other gram neg enteric pathogens cause septic arthritis in?
Immunocompromised, elderly
What is the most common cause of genearlized MSK pain in women 20-55yo?
Fibromyalgia
How is diagnosis of fibromyalgia made and what are common sites?
Widespread MSK pain and excessive tenderness to palpation of at least 11 of 18 predefined soft tissue locations during PE - sites include upper quadrants of butt and medial aspects of knee, SCM, trapezius. Will have absence of joint swelling and worsening with exercise. Pain but no weakness. Also common to have fatigue, IBS, depression. No inflammation, joint swelling, or weakness and no abnormalitites on labs
How can differentiate pts with seronegative spondyloarthropathies vs fibromyalgia?
Seroneg: Neg RF but elevated ESR. Pain improves with exercise (vs fibromyalgia)
Who is polymyalgia rheumatica most common in? S/S? Labs?
Women and pts >50yo. Present with pain and stiffness of shoulders and pelvic girdle. ESR almost always elevatd. Commonly assoc with temporal arteritis
What are s/s of polymyositis? Lbbs?
Symmetric proximal muscle weakness and mild pain. Elevation of CK and inflammation of muscle fibers
What are risk factors for rheumatoid arthritis? How present?
Female gender, middle age are risk factors. Swelling of wrist and hand joints (MCP, PIP), morning stiffness, elevated RF and ESR are common
Who is Sjogrens most common in. What are clinical findings? How is diagnosis made?
Autoimmune, most common in women in 5th-6th decade of life. Clinical findings: keratoconjunctivitis sicca (xerophthalmia, dry eyes) and xerostomia (dry mouth). Due to antimicrobial and lubricating properties of normal saliva, pts will have inc dental caries and complain of difficulty swallowing. Lymphocytic infiltration of salivary glands causes enlargement and firmness to palpation of these glands. Dx: subjective and objective evidence of dry mouth and eyes in presence of either histologic evidenc of lymphocytic infiltration of salivary gland sor serum autoAb directed against SSA (Ro) and/or SSB (La)
When are antimitochondrial Ab positive?
Primary biliary cirrhosis (autoimmune diseas characterized clinically by progressive jaundice, varices, and other signs of cirrhosis)
What is Barrett esophagus?
Metaplasia of esophagel squamous epithielium to columnar epithelium; is a precursor of esophageal adenocarcinoma
What is the MCC of lumbar spinal stenosis aka neuropathic claudication? What are s/s, how differentiate from PVD, and how make dx?
DJD is MCC; results from any condition that narrows the spinal canal and compresses nerve roots, most commonly seen in middle-aged and elderly adults Exacerbation of leg symptoms with walking (similar to PVD) but unlike PVD, the symptoms are positional and remain while standing still and is better when walking uphill and sitting. Pain relieved by flexion of spine (widenes spinal canal). Can see weakness, sensory loss, numbness/tingling, discomfort of legs; neuro normal and only 10% have positive straight leg test. Dx: clinical history and classic findings on spinal MRI (bony anatomy, neural structures, soft tissue)
What are ankle-brachial index used for?
To evaluate for PVD
How does PVD present?
Leg and butt pain worse with activity and relieved by rest. Pulses decreased
What does ankylosing spondylitis present as?
Young amles (15-30yo with lower back pain with limited spinal mobility. Improvement with exercise. +HLA-B27
What are the 2 most common forms of inflammatory mypoathy? When do they occur and in what gender more commmonly? How do they present and how to distinguish from other causes of myositis? How dx and tx?
Polymyositis and dermatomyositis. Present with proximal muscle weakness (gradual onset), +ESR and CK, dx with muscle bx. MC in 40-50yo F>M. Similar presentaiton sin drug-induced myoatphy (caused by statins, antipsychotics, alcohol), hypothyroid myopathy, muscular dystrophy, MG. +ESR and +CK are supportive of inflammatory myositis. Tx with high dose steroids
When is Colchicine used?
Acute flares of gouty arthritis. Inhibits Neutrophil activity
What is indomethacin?
Potent NSAID
What is Riluzole?
Used to slow progression of ALS (progressive weakness of arms, legs, CN with a mix of UMN and LMN signs)
What can TCAs do for pain?
Dec pain in fibromyalgia (do nothing for muscle weakness)
What is pyridostigmine?
Anticholinesterase used to treat MG. Most pts with MG have facial and ocular muscle weakness
What is the most common cause of asymptomatic elevation of alkaline phosphatase in elderly pt?
Pagets disease of bone (osteitis deformans) - typically asymptomatic at time of dx and dx made incidentally with isolated elevated alk phos on routine lab testing
What are causes of inc alk phos?
MC seen in hepatobiliary disorders or disease of bone causing inc bone turnover. MC is Pagets disease.
What are most commonly affected bones in Pagets disease? What are complications?
Skull, clavicles, pelvis and long bones. Pahtologic fractures, pain, osteosarcoma, neuro symptoms are complications.
What is PSA usually in prostate cancer?
>4.
In pts with bone mets, what will be lab changes? Presenting s/s?
Inc alk phos but will also have hyperCa due to bone resorption. Will also have bane and osteoblastic lesions on x-ray.
What are s/s of multiple myeloma?
Bone pain, hyperCa due to osteolysis. Monoclonal Ig proteins in serum and urine. Weakness, fatigue, wt loss, renal disease, amyloidosis not uncommon.
What are SE of statins?
Inc AST, ALT. Rhabdo leading to myoglobinuria and renal failure
What are LFT changes in alcoholic liver disease?
Inc in AST and ALT but 2:1 AST:ALT
How does viral arthritis present? What is MCC?
Acute onset of polyarticular and symmetric arthrits that resolves within 2 months. MCC: Parvovirus B19, esp in adults with frequent contact with children, such as daycare workers. Parvo B19 common involves MCP, PIP, wrisk joints and "slapped cheek" appearance is rare in adults
How can tell the difference between rheumatoid arthrits and viral arthritis?
Rheumatoid: MCP, PIP, wrist (same as viral from Parvo B19). But, viral is more acute onset with morning stiffness <30min and lack of joint swelling or systemic symptoms. Rheumatoid needs to be present for at least 6 weeks to diagnost, morning stiffness >30min, and usually systemic signs
What are s/s of SLE?
arthritis, rash, hematologic abnormalities, renal disease, fever, wt loss, inc ESR
Where does psoriatic arthritis usually affect and what does it look like?
DIP joints. Dactylitis ("sausage digit"), nail findings, psoriasis of skin are characteristic
How does acute rheumatic fever present?
Polyarthritis, carditis, chorea, erythema marginatum, subcutaneous nodules. Arthritis is often migratory in nature and usually first affects the joints of the lower extremities
How can gonococcal septic arthritis present?
1 of 2 way: asymmetric polyarthritis (often assoc with tenosynovitis and skin rash) or as an isolated purulent arthritis affecting one or few joints
What is purulent arthritis in sexually active pt until proven otherwise?
Gonococcal arthritis
How dx gonococcal arhtriits?
Gram stain of synovial fluid, blood, cultures, urethral cultures.
When does acute rheumatic fever occur after pharyngitis? What is the organism? What are s/s?
2-4 weeks after paryngitis by Group A strep. Symptoms: migratory arthritis of large joints, erythema marginatum rash, subcutaneous nodules, carditis, Sydenham chorea
When do symptoms of acute HIV infection tend to present and what are the s/s?
2-4 weeks after exposure to virus. Symptoms: non-specific and include fever, arthralgias, sore throat, LAD, mucocutaneous lesions, diarrhea, wt loss
How does crystal-induced arthritis usually present and what does tap show?
Warm, painful, swollen joint accompanied by low-grade fever. Joint tap: WBC of 10,000-50,000 and characteristic crystals under polarized light
What are s/s of infective endocarditis?
Fever, new murmur, Osler's nodes (nodules on finger and toe pads), Roth's spots (retinal hemorrhages), and Janeway lesions (small hemorrhages on extremities)
What are causes of reactive arthritis and what is presentation?
GU infection with Chlaymdia or by certain GI infections. Presents with triad of arthritis, conjunctivitis, urethritis
SLE - who is at most risk. What are s/s. What labs are specific?
Women in 20s and 30s at highest risk. S/S: malar "butteryfly" rash, arthritis, painless oral ulcers, renal disease. Positive anti-DS DNA is very specific.
What is one of the leading causes of M/M in SLE? How should you base treatment?
Renal disease (40-75% of pts). Spetrum is wide. Need to do renal bx in pts with lupus nephritis bc different forms have different treatments. In addition, initial bx provides baseline histology against which future biopsies may be compared to monitor disease progression - if delay renal bx, may adversely affect outcome
What are red flags for lower back paind and what might they suggest?
Red flags: >50yo, previous hx of cancer, unexplained wt loss, pain >1mo duration, nighttime pain causing difficulty with sleep, no response to previous therapy, neurologic symptoms, fever, lack of exacerbation with movement or palpation. May suggest systemic disorder, herniated disk, or bony abnormality such as lytic lesions and compression fractures
What does pain to palpation of vertebra on exam suggest?
Spinal infection or possibly lytic lesion of the spine
What does positive straight leg test on exam suggest?
Herniated disk
What is the test of choice to further evaluate back pain in pt with red flag?
Plain film looking for lytic lesions or compression fractures. If neg and still high clinical suspicion, get MRI of back or CT scan to evaluate for possible disc disease, cancer, spinal infections.
What are the most common cancers to mets to bone?
Lung, breast, prostate, renal, multiple myeloma, thyroid
When is MRI of back more sensitive than CT?
Detection of infection and cancer. Indicated for progressive neurologic deficits, high suspicion of cancer or infection, and symptoms >3mo
When should refer back pain pt to ortho or neuro surgeon?
Cauda equina syndrome, spinal cord compression, progressive neurologic deficits, or persistent pain after conservative therapy.
When should pts on NSAIDs for back pain get imaging?
After failing treatment for 2 weeks (earlier if have red flags).
Is PT more affective than NSAIDs?
PT effective in chronic back pain but not as effective as NSAIDs in treatment of acute lower back pain
How does gouty arthritis occur and pts on what therapy are at risk?
Results from overproduction or underexcretion of uric acid. Induction chemo results in rapid tumor lysis and releases uric acid into the circulation.
How do you prevent and treat gout?
Prevention with allopurinol and probenecid (inc urinary excretion of uric acid but 2nd line bc of inc risk of uric acid renal stones). Treat acute attacks with colchicine, NSAIDs, steroids
What is the most common presentation of gout?
Acute, monoarcticular arthritis affecting 1st metatarsophalangeal joint (podagra).
How do you diagnose gout?
Definitive dx with joint aspiration with demonstrated needle-shaped, negatively birefringent urate crystals and a WBC count of 2,000-50,000.
What is the MOA of allopurinol?
Xanthine-oxidase inhibitor -> dec uric acid production
What does urine acidification do?
Eliminates amphetamines. Will increase gout attacks by increasing uric acid solubility and decreases uric acid renal stone formation.
What is N-acetylcysteine used for?
Antidote for acetaminophen OD and as a nephroprotective agent to prevent radiocontrast-induced nephropathy
What is Mensa and what is it used for?
Prevents hemorrhagic cystitis caused by certain chemo agents (cyclophosphamide)
What is Behcet's syndrome, who does it occur in, and what are s/s?
Multi-systemic inflammatory condition characterized by recurrent oral and genital ulcers and skin lesions. MC seen in Turkish, Asian, and Middle Eastern Population. Combined environmental and hereditary factors play a part in pathogenesis. International criteria for dx: Recurent oral ulcers + 2 of the following: recurrent genital ulcers, eye lesions including anterior uveitits and posterior uveitis, retinal vascularization, skil lesions including erythema nodosum, acneiform nodules and papulopustular lesions, +pathergy test. Some pts have involvement of GI, skeletal, and vascular systems. Tx; steroids offer relief from most symptoms, but no protection for progressoin to dementia or blindness
What is erythema nodosum?
Red nodules that are tender and warm
What should suspect in pts with bilateral ankle arthritis and bilateral hilar adenopathy on CXR?
Sarcoidosis
Who is sarcoid most common in?
Black women in 3rd-4th degades
What is the skin lesion of sarcoid?
Erythema nodosum
What is reactive arthritis?
Urethritis, conjunctiviits, and arthritis, as well as mucocutaneous lesions (stomatitis, balanititis, keratoderma blennorrhagicum). Usually follows dysenteric infection or STD (Chlamydia)
What does herpes look like?
recurrent small grouped vesicles over orolabial and genital areas.
What is SLE?
Rheumatic disease characterized by auto-Ab directed against self-antigens. Malar rash, arthritis, oral ulcers, other systemic involvement. Clinical course has spontaneous remissions and recurrences
How does polymyositis present?
inflammatory disease of unknown etiology. Presents initially with slowly progressive proximal muscle weakness of the lower extremities characterized by difficulty ascending and descending stairs or rising from a seated position. The weakness usually progreses over the course of years; an acute presentation is not typical. Proximal arm weakness usually follows leading to complaints of difficulty with combing hair or working with hands overhead. Usually no skin findings (vs dermatomyositis). Muscles of mastication and facial expression are classically spared, but mya develop dysphagia due to involvement of striated muscles of upper pharynx. Weakness is primary complaint, and while muscle tenderness may be present, severe tenderness or tenderness i absence of weakness should lead to consideration of other dx such as PMR.
How dx polymyositis?
Muscle bx is best diagnostic study. MRI can assist in identifying best place to bx. Bx shows mononuclear infiltrate surrounding necrotic and regenerating muscle fibers. In more advanced disease, an inflammatory infiltrate may be absent and replacement of muscle with fibrotic tissue may be evident.
When is MRI of the spine helpful?
Identifying conditions that may cause compression of SC or spinal nerve roots such as herniated discs or spinal stenosis.
When do you do EEG?
Seizures, sleep disorders
When is temporal artery bx helpful?
Necessary to make dx of temporal arteritis
When is LP useful?
To dx meningitis, subarachnoid hemorrhage, and inflammatory conditions of CNS such as MS
What does x-ray of osteoarthritic knee show?
Narrowed joint space, osteophytes, subchondral sclerosis or cysts.
What is the biggest risk factor for osteoarthritis?
Obesity - wt loss decreases joint pain, increases function, and slow progressoin of disease
How do pts with osteoarthritis present?
Brief morning stiffness (<30min), exertional joint pain. Usually no symptosm of fever and wt loss
What is the most readily modifiable risk factor for osteoarthritis?
Weight loss - slows progression and improves joint pain and function. Meds and exercise play a role, but only with temporary relief. PT helps to strengthen muscles and redues pain and improves mobility, but doesn't slow progression of OA
What are anti-topoisomerase-I ab for?
Systemic sclerosis
What are anti-smooth muscle ab for?
Autoimmune hepatitis
What are anti-neutrophil cytoplasmic Ab for?
Granulomatosis with polyangiitis (Wegener's) - a form of granulomatous vasculitis.
When is RF classically positive?
Rheumatoid arthritis, but can also be inc in SLE, Sjogrens, dermatomyositis, HCV infection, and others
What are the manifestations of systemic sclerosis?
Heterogeneous condition that can affect every organ system in the body. Skin: skin thickening (begains at acral sites (hands and feeet) with edema that transitions to dermal sclerosis with obliteration of skin appednges (hair follicles and sweat glands) and flexion contractures. Rheumatoid phenom and calcinosis cutis are also commonly observed. The face may take on a "mask-like" appearance due to dermal thickening. CT thickening, the product of myofibroblast proliferation and inc collagen and ground substance production, is the underlying pathogenesis of may features of systemic sclerosis. Involvement of kidneys produces hypertension, and before the advent of ACI, scleroderma renal crisis was the MCC of death in these pts. Pulmonary arterial HTN ulimtately results in RHF. Esophagela and gastric dysmotility causes GERD. Anti-nuclear AutoAb present in all scleroderma pts, anti-topoisomerase-I Ab also.
What are the most common complaints of sarcoid pts who present symptomatically?
MC: cough, dypsnea, fever, wt loss. WHile lungs are most common involved organ system, the skin (erythema nodosum), eyes, (anterior uveitis), joints (arthritis), and many other organ systems may be affected. CXR: bilateral hilar adenopathy and reticular opacities.
What do you see in slit lamp of anterior uveitis?
Red eye with leukocytes in anterior chamber
What are symptoms of acute HIV infection?
Non-specific. Fever, arthralgias, sore throat, LAD, mucocutaneous lesions, diarrhea, wt loss.
What part of the eye does histoplasmosis damage?
Retina
What eye problem can you get with ankylosing spondylitis?
Anterior uveitis
What are s/s of Hodgkin's lymphoma?
Common in young adults . Painless, swollen LN and hilar adenopathy. B symptoms - fever, wt loss.
How can you get gout from myeloproliferative disorder?
Myeloproliferative disorders are common causes of uric acid overproduction bc they inc catabolism and turnover of purines -> inc in serum uric acid levels
What changes does polycythemia vera cause in terms of spleen and pruritis?
Splenomegaly, characteristic pruritis with hot baths due to histamine rleae from an inc number of circulating basophils.
What is a common arthritis in polycythemia vera pts?
Gout (up to 40%)
How does CKD cause gout attacks?
Decreases the amout of uric acid excreted in the urine
What is hemochromatosis (symptoms, cause)?
Autosomal recessive iron overload syndrome most often due ot mutation of HFE gene. Symptoms: related to iron accumulation in various organs: hepatic dysfunction progressing to cirrhosis, diabetes, hypogonadism, skin pigmentation, arthritis
What is Lesch-Nyhan syndrome?
Caused by a genetic deficiency of the enzyme HPRT (hypoxanthine-guanine phosphoribosyl transferase) - characterized by overproduction of uric acid, behavioral problems (esp self-injurious actions), and neurologic disability and is generally diagnosed in chilhood.
What are the complications of high Ca in hyperPTH?
chondorocalcinosis and CPPD disease (pseudogout) - positively birefringent crystals
What type of anemia does pernicious anemia cause?
Macrocytic (with neurologic abnormalities)
How does portal HTN cause severe pruritis?
Inc serum concentrations of bilirubin.
When should suspect temporal arteritis?
>50yo pt with new headache, jaw claudication, scalp pain, visual loss, or symptoms of PMR. It is a large vessel vasculitis that affects aorta and its cranial arterial branches. Vision loss is one of the msot feared complications of temporal arterities (up to 20% of pts)
How treat temporal arteritis?
Prompt systemic high dose steroids to lower rate of visual complications and dec likelihood of visual loss in inaffected eye. Note: PMR treated with low-dose steroids.
How dx temporal arteriitis?
temporal artery bx. ESR will be elevated
What is acetazolamide used for?
open-angle glaucoma and beneign intracranial HTN
How can distinguish gout from pseudogout?
Not by history and physical. Need synovial fluid analysis. Pseudogout - rhomnoid, positively birefringent crystals and radiographic evidenc eof chondrocalcinosis. Gout: needle shaped, negatively birefringent crystals.
What type of crystals cause pseudogout?
CPPD (calcium pyrophospahte ihydrate crystals)
How do attacks of pseudogout often occur?
Truama, surgery, medical illness
What is the common presentation of pseudogout?
Acute pain, swelling, redness, limited motion of affected joint(s). Knee most common (>50%). can also ahve fever, leukocytosis with L shift, and chondrocalcinosis (calcified artericualr cartilage).
What is hydroxyapatite and where can see it?
Colexed form of Ca found in teeth and bones. It can also exist in cartilage of pts with degenerative osteoarthritis and may be isolated from synovial fluid in such pts
What type of crystals do you see in gout?
Monosodium urate crystals
What is the msot common crystal foudn in renal calculi?
Calcium oxalate crystals
When are struvite stones found and what are they made of?
Magnesium ammonium phosphate crystals. Found in renal calculi of pts with UTI cause by urease-producing organisms (Klebsiella, Proteus)
How can distinguish viral arthritis from other types?
Symmetric small joint inflammatory arthritis. Tends to resolve within 2mo. Can have +ANA (weakly pos) and +RF. Treatment: NSAIDs for resolution of symptoms. Antivirals un-necessary bc self-limited. Causitive agents: Parvovirus, hepatitis, HIV, mumps, rubella.
When does osteoarthritis occur (onset) and do you ahve a fever?
No fever bc non-inflammatory. Insidoius onset typically >40yo
What type of arthritis can pts with sarcoid have?
Polyarthrits - most often in ankles and knees
What are the seronegative spondyloarthropathies?
Ankylosing spondylitis, reactive arthritis, psoriatic arthritis. Asymmetric arthritis and inflammatory back pain with neg RF
How does PMR present?
>50yo, inflammatory condition with sore and stiff muscles, esp in neck and shoulders. ESR usually >40, nL ANA
What is the classic triad of disseminated gonococcal infection? What other s/s can you have and what is often in the history?
Polyarthralgias, tenosynovitis (pain elicited along tendon sheaths), vesiculopustular skin lesions (anywhere from 2-10 and may be dismissed as furuncles or pimples). Fever and chills can be present. Hx of recent unprotected sex with new partner is frequent, while symptoms of symptomatic venereal diases is most often absent.
What is the rash and arthritis of Lyme disease?
Rash (erythema migrans) occurs early on with bulls eye appearance, while artrhitis (typically monoarticular knee pain) doesn't cocur until months later.
What are the skin findings of syphillis?
Painless ulcer of genitalia that occurs in primary stage of infection and maculopapular rash of palms and soles in secondary stage
What are the s/s of meningococcemia?
Petechial rash, high fever, HA, N/V, stiff neck, photophobia.
What is erythema marginatum and when do you see it?
Raised ring-shaped lesions over trunk and extremities. Seen in acute rheumatic fever ?and others?
How does osteoarthritis typically present in hip?
>40yo with indolent course - progressive anterior hip pain (can be described as groin pain)exacerbated by walking adn relieved by rest. Morning stiffness/stiffness after prolonged resting is consistent, but morning stiffness lasts <30-60min (as opposed to rheumatoid). Active and passive internal and external rotation is limited and tenderness to palpation and systemic signs are absent. Pain at rest or overnight occurs on in advanced disease. Etiology is progressive mechanical destruction of the articular cartilage leading to bone-to-bone friction and formation of osteophytes.
What is th emost common joint disease and what are predisposing factors?
Osteoarthritis. Advanced age and obesity, esp for hips and knees
What is meralgia paresthetica?
Condition where compression of the lateral femoral cutaneous nerve causes lateral hip paresthesia unaffected by motion or palpation.
What causes trochanteric bursitis? What are presenting s/s?
Caused by friction between the tendons of the gluceus medius and tensor fascia lata over the greater trochanter of teh femur. Pain localized to lateral hip, worsened by palpation. Pain casued by pressure on the lateral hip may interfere with sleeping
What is osteonecrosis of the femoral head often assoc with?
Chronic corticosteroid use
When referred pain from the lumbosacral area causes posterior hip or gluteal pain and when impingement of the lumbar nerve roots causes pain to radiate laterally down the thigh, waht will you see on exam?
No limitation of hip mobility but +findings on straight leg raise.
What is the most reliable sign for spinal osteomyelitis? What are other features? What is most sensitive test? Who is at inc risk?
Most reliable sign: Tenderness to gentle percussion over the spinus process of the involved vertebra. Pain is not relieved by rest. Fever and inc WBC are unreliable. ESR grossly elevated (>100). MRI most sensitive study. Very high index of suspicion in pts with history of IVDA or recent distant site infeciton (ex: UTI).
Who is at highest risk for osteomyelitis?
IVDA, sickle cell pts, immunocomprmoised
What is MC organism in IVDA with osteo?
Staph aureus, but gram neg also common.
What is tx of spinal osteomyelitis?
Long term IV abx with or without surgery
What are the s/s of ankylosing spondylitis?
Pain and progressive limitation of back motion. Usually max in morning and improve as day goes along
How does lumbar disk hernitation present?
Acute onset of back pain with or without radiation down a leg. Pts can often recall an inciting event. Worse with activity, improves with rest. Spine not tender to palpation
What is the definition of lumbar spinal stenosis? Who is it most common in? How does it present?
Narrowing of spinal canal with compression of 1 or more spinal roots. >60yo. Back pain that radiates to butt and thighs. Symptoms worse with walking and lumbar extension and improve with lumbar flexion. Can have numbness and paresthesas. Dx: MRI
When do you worry about prostate cancer bone mets?
Older age, night pain, urinary symptoms
How do vertebral compression fractures present?
Local tenderness to palpation, usually in elderly pt with history of osteoporosis
What are pts with ankylosing spondylitis for >20 yrs at inc risk for when falling?
Vertebral fractures due to dec bone mineral density. Can occur with iminmal trauma so have suspicion if have longstanding AS
How does lower back pain of AS present?
Insidious, unilateral, intermittent pain that may beocme bilateral with persistent flares. Pain is not typically sudden and severe
How does pain of spinal root compression present?
Dermatomal distribution with sensory loss, paresthesias, and weakness of muscles innervated by the inolved nerve root
What are pts with AS at inc risk for in terms of muscles?
Muscle spasms - present with sudden severe back pain that resolves within second to minutes and may recur
When can have referred visceral pain to back?
Pancreatitis, Abdominal aortic dissection
What MCC of bone malignancies?
Mets to bone (more common than primary bone cancers)
What is the pathophys of secondary amyloidosis and what can it be secondary to?
Extracellular deposition of insoluble polymeric proteinf ibrils in tissues and organ with elevated amyloid A. Can be secondary to chronic inflammatory conditions: inflammatory arthritis (RA), chronic infections (bronchiectasis, TB, osteo), IBD, malignancy (lymphoma), vasculitisi
What is the clinical presentation, dx, and tx of secondary amyloidosis?
Presentation: asymptomatic proteinuria or nephrotic syndrome, CM with heart failure, hepatomegaly, mixed sensory and motor peripheral neuopathy an/dor autonomic neuropathy, visible organ enlargement (ex: macroglossia), bleeding diathesis, waxy thickening, easy bruising of skin. Dx: abd fat pad aspiration bx. Tx: treatment of underlying condition. Colchicine for prevention and tx
What is hepatorenal syndrome?
Acute renal falure in pts with acute or chronic liver disease and portal HTN. Usually presents in pts with severe liver disease with progressively rising serum Cr and minimal proteinuria (<500mg/day)
What is hypertensive nephrosclerosis?
Seen in pts with chronic HTN and associated with retinoapthy, LV hypertrophy, progressive renal failure, and mild proteinuria (<1g/day). Kidneys are usually small
What is IgA nephropathy?
Type of nephritis that typiclaly presents with hematuria on UA. Restricted to kidneys
How do pts with PCKD present?
Flank pain, hematuria, renal failure, HTN, large palpable kidneys. Can also hve hepatic cysts
What does synovial fluid anaylsis of OA reveal?
<2000 WBC, no organisms or crystals
How does OA present?
noninflammatory (no fever), affects hands and weight bearing joints. mild morning stiffness <30min, exacerbated by exercise and relieved by rest. No systemic symptoms. Can have effusions but wont' be hot to touch. Exam: bony crepitus, bony enalrgement, painful/dec ROM are common. X-ray: narrowed joint space with osteophyte formation and subchondral sclerosis/cysts
When do you see punched out erosions with rim of cortical bone on x-ray?
Gout y arthritis
When do you see periarticular osteopenia and joint margin erosions on x-ray?
Classic for RA
What is cell count in RA?
2,000-50,000
How does RA present?
morning stiffness >30min, systemic symptoms of fever, malaise, wt loss. Joints: wrists, MCP, PIP. Joints warm to touch
What will see on x-ray in pts wth infectious arthritis?
Normal joint space with soft tissue swelling
When do you see calcification of cartilaginous structures on x-ray?
(chondrocalcinosis) - see in pseudogout
What is the presentation of dermatomyositis and what are they at risk for?
Proximal muslce weakness with cutaneous findings - violaceous poikiloderma over various regoins of body. On face, reuptions most often accompanied by periorbital edema and is known as heliotrope sign; on chest and lateral neck, called shawl sign; on knuckles, elbows, and knees it is Gottron's sign. Lichenoid papules overlyoing joints are known as Gottron's papules and are pathopgonominc for DM. At risk for internal malignancies - most common is ovarian, but breast, lung, other female urogenital cancers may occrs as well - essential to have regular age-appropriate cancer screening
Who is dermatomyositis mroe common in and what is the Ab test?
F:M 6:1. anti-Mi-2 Ab (against helicase)
What inflammatory disorders are assoc with aortic aneurysms?
Behcet's, Takayasu arteritis, giant cell, ankylosing spondylitis, RA, psoriatic arthritis, relapsing polychondritis, reactive arthritis
What autoimmune disease are assoc with renal failure?
SLE, scleroderma, Goodpasture, relapsing polychondirits, Wegeners (granulomatosis with polyangiitis)
What inflammatory disease are assoc with alveolar homoerrhage?
Goodpastures, Wegeners, polyarteritis, Churg-Strauss, Behcets, anti-PL Ab syndrome
What inflammatory/depositional disease are assoc with carpal tunnel syndrome?
Rheumatoid arthritis, sarcoidosis, amyloidosis.
What autoimmune diseaseas are assoc with sudden visual loss?
Temporal arteritis and rarely SLE
What meds are effective in fibromyalgia?
Amytriptyline and cyclobenzaprine - they can inc amt of restorative phase 4 sleep. In pts with depression as well, can also give SSRIs
What joint problems is methotrexate used for?
inflammatory arthritides such as RA or psoriatic arthritis
What is a vessel complication of giant cell/temporal arteritis? How can prevent?
Aortic aneurysms bc of involvement of branches of aorta. Pts should be followed with serial CXR
What are s/s of giant cell arteritis?
HA, jaw claudication, muscle fatigue, visual disturbance, scalp tenderness on exam, dec temporal artery pulse. ESR >50.
What is the MC form of leukemia in older pts?
CLL. Insidious onset.
What is the MCC of hypothyroid?
Chronic lymphocytic thyroiditis (Hashimotos).
Does radiation to thyroid region predipose to development of hypothyroid?
Yes
Who is ulcerative colitis more common in?
Jews, +Fhx
What are teh important causes of membranous glomerulonephritis?
Hep B and C, syphilis, gold, penicillamine, SLE< RA. Many pts have no predisposing factors
What are tophi?
Collecions of urate cyrstals which form firm, yellowish nodules at the sites of involved joints in pts with chronic gout.
What is the MCC of septic arthritis?
Staph aureus
Is RA symmetric?
Yes
When do you see Heberden nodes?
DIP joints in osteoarthritis. They form from calcified cartilagenious spurs
What accounts for the MSK complaints in reactive arthritis?
Lower extremity oligoarhtirits and enthesopathy (inflammation at gendon and ligament insertions)
What causes rotator cuff injuries? What s/s are suggestive? What should use for diagnosis?
Can result from chronic rotator cuff tendonitis and should trauma. Shoulder pain and weakness when lifting arm above head is suggestive of rotator cuff pathology. Also, lying on affected side hurts. Limitation of mid-arc abduction and external rotation are common findings on exam. Lidocaine injection will improve rotator cuff tendonitis, but not rotator cuff tear. MRI is excellent for visualizing soft tissue structures and is study of choice for diagnosing rotator cuff tears.
What is classic presentation for how tore rotator cuff?
Fall on an outstreatched arm.
How is x-ray helpful in shoulder injuries?
inexpensive way to diagnose fractures, dislocations, and calcific tendonitis, but can't do soft tissue
How does multiple myeloma present?
pain in spine, ribs, back. Can be accompanied by hyperCa and anemia. dx: BM biopsy
What are bone scans used for?
Diagnosing osteomyelitis, fractures, metastatic disease.
Describe the joint mainfestations of SLE
<90% of pts have joint involvement, most commonly affecting the hands or knee. It is a migratory arthritis taht is often disproportionate to objective physical findings Joint pain is common, but the arthritis induced by SLE is considered non-deforming.
What are common presentations of SLE?
Low-grade fever, weakness, wt loss, rash (malar butterfly, annular, disoid), arthralgias/arthritis, proteinuria, hematologic abnormalities. Inc ESR (nonspecific but suggests systemic inflammation consistent with SLE).
When do you see subluxation of cervical vertebrae and tendon damage in hands?
Rheumatoid arthritis
When do you see cartilage degradation?
Osteoarthritis. Advanced age and obesity, esp for hips and knees
When do you see distal phalangeal respotion?
Prominent in arthritis mutilans variant of psoriatic arthritis leading to classic "pencil-in-cup"deformities
Describe the presentation of PMR
Pain and stiffness in neck, shoulders, and pelvic girdle in pts >50yo with elevated ESR and morning stiffness lasting >1hr. PE: unremarkable with denying of tenderness with active or passive mortion. No signs of joint inflammation.
What is treatment for PMR not assoc with giant cell arteritis?
Low dose prednisone (high dose if also have giant cell)
What are features of giant cell arteritis?
Headache, jaw-claudication, visual changes, abnoramlities of temporal artery, constitiutional symptoms
When do you see positive ANA?
SLE, drug-induced lupus, RA, mixed CT disorders, polymyositis, other autoimmune conditions
What are important non-medication measures to prevent future attacks of acute gouty arthritis?
Alcohol cessation, low purine diet. Ethanol -> lactate - lactate competes with urate for renal excretion -> accumulation of urate in body. Also, avoid drugs such as diuretics and pyrazinamide
What is treatment of acute attack of gout?
NSAIDs (DOC), colchicine, or steroids
What is the pathogenesis of spinal stenosis?
combo of 2 factors: enlarging osteophytes at faget joints and hypertrophy of ligamentum flavum
What does iliac artery atheroscelrosis cause?
Claudication in butt and thighs. Typically pain relieved by rest, exacerbated by activity. No positional component like in spinal stenosis
How does lumbar disk hernitation present?
Acute onset back pain w/ or w/o radiation down 1 leg. Usually recall inciting event. Pain may radiate and may be assoc with neurologic symptoms. Lumbar flexion, sitting makes the pain worse
What is spina bifida occulta?
Congenital defct of vertebral arch that doesn't involve protrusion of the cord or dura. Typically asymptomatic and dx as incidental radiographic finding
How does mets to vertebrae present?
Pain that is chronic, dull, worse at night, chnages little with activity, nonradiating
What causes Pagets disease?
Disorder of inc bone turnover - Osteoclast dysfunction leads to inc bone breakdown and compensaotry inc in bone formation which results in a "mosaic" pattern of lamellar bone, inc alk phos level, and x-ray findings like femoral bowing. Joint and bone pain, skeletal deformities, and hearing loss are common symptoms. Often asympatomic and only identified incidentally on x-ray or with elevated alk phos. Enlarging cranial bones can lead to inc hat size or entraped CN 8 -> hearing loss
When do you see osteoblast dysfunction?
Diabetes, osteoporosis (pagets is osteoclast dysfunction)
When do you see overproduction of calcitriol (active form of vit D)?
Granulomatous disease (sarcoid, TB). May have hypercalciuria and hyperCa as well
What are s/s of hyperPTH?
kidney stones, abd pian, malasie, osteoporotic bone changes
What are changes in calcium absorption in pts with GI disease like celiac?
Require higher intake of Ca and vit D to prevent osteoporotic bone changes
How do you treat symptomatic sarcoidosis?
Corticosteroids. No tx if asymptoamtic bc of high rate of spontaneous remission
What are manifestations of sarcoidosis?
Lung involvement - cough, dyspnea, x-ray which shows hilar/paratracheal adenopathy with or whitout reticulonodular infiltrates and bx which show noncaseating granulomas. Erythema nodosum, anteiror uveitis, acute polyarthritis. May have high ACE level
When is hydroxychloroquine used?
Malaria prophylaxis and to treat acute malaria, RA, and SLE
What is infliximab and when is it used?
TNF-alpha blocker approved to treat IBD, AS, and RA
What is itraconazole used to treat?
Histompalsmosis (bx shows yeast)
When is cyclophosphamide used?
SLE with renal involvement and as a chemo drug
What are INH and rifampin used for?
4-drug regimen for active TB
What is erythema nodosum? When do you see it?
Painful, subcutaneous, pretibial nodules . Can be a symptom of a more serious disease process including sarcoid, TB, histoplasmosis, recent strep infection, IBD.
What is the MCC of erythema nodosum?
Recent strep infeciton
What is the initail workup for erythema nodosum?
Symptom guided, includes CXR (for sarcoidosis, TB), PPD skin testing, ASO titer (for recent strep infection)
How does RA present?
Progressive and symmetric involvement of peripheral joints. Common sites of early involvement include MCP and PIP joints of fingers, metatarsal joints of toes, and wristk joinst. MC affects the cervical spine joints in the axial skeleton and can cause spinal subluxation and spinal cord compression
What are the symptoms and exam of RA?
Symptoms: indisious onset, multiple joint pain with stiffness and swelling, morning stiffness lasting hours, improves with activity, small joints (PIP, MCP, MTP) commonly involved, monoarthritis (ex: knees, elbows) can also occur later, SPARES DIP joint, unlike OA. Exam: affected joints are tender to the touch, swollen, with limited range of motion, tenosynovitis of the plams -> "trigger finger", Rheumatoid nodules (esp on elbows), cervical joint involvement can lead to spine subluxation -> spinal cord compression.
What are the lab/imaging study findings in RA?
Positive anti-CCP testing (diagnostic testing, High IgM Rheumatoid factor, high CRP and ESR correlates with disease activity, x-ray show soft-tissue swelling, joint space narrowing, and bony erosions
Who is RA more common in?
F:M 2-3:1. Peak age 50-75yo
What is a sensitive sign of early disease on RA?
Reduced grip strength - can occur occasionally and is a sensitive sign of early disease
How do pts with RA with cervical spine involvement present?
neck pain, stiffness, radicular pain in the upper exremity. Subluxation of the SC compression can present with hyperreflexia or upgoing toes on Babinski
What part of the spine is the most common site of disc herniation and spinal stenosis?
Lumbar spine
What types of arthritis cause sacroiliac involvement?
Sernoneg spondyloparthropaities (AS, reactive arthritis, psoriatic arthritis)
What is the approach to pts with acute "mechanical" back pain (and what does that mean) without significant neurologic deficit?
Conservative approach for 4-6 weeks - this includes early mobilization, muscle relaxants, NSAIDs. Bed rest, exercise, and PT are not shown to be helpful. If pain continues after 4-6 weeks of conservative management or progressive neurologic deficit evolves, high-resolution diagnotic modalities are usually employed - MRI and CT with or without contrast myelography. mechanical back pain - ex could be positive straight leg test that suggests disk herniation but with no neurologic deficit and perianal area is intact
When is emergent surgical decompression indicated in back pain?
In cases of significant or rapidly progressive neurologic deficit (foot drop, weakness of the legs)
When is plain roentgenogram used?
Pts with osteoporosis and possible vertebral crush fractures.
What are s/s of UC and what arthritis can it be related to?
Acute onset bloody diarrhea, anemia, neg stool cultures. Typically presents in pts during 2nd-3rd decade, presenting symptom of UC often bloody diarreha, lower abd pain, tenesmus. Common extracolonic manifestations include skin findings, erythema nodosum, pyoderma gangrenosum, episcleritis, arthirits, cholangitis. P-ANCA positive in UC. IBD may occur in assoc wtih inflammatory arthritis - anklyosis spondylitis and IBD are both assoc with HLA-B27 and may occur in association with one another. Both can also be assoc with positive p-ANCA despite absence of vasculitis in both conditions
What GI infections can cause reactive arthritis?
Shigella, Salmonella, Yersinia, Campylobacter, or C. diff. Reactive arhtiris - uerthritis, conjunctiviits/uveitis, arthritis, maalise, and characteristic cutaneous findings (keratoderma blennoffhagica and balantitis circinata)
What does infection with Tropheryma whippelii cause?
Whipple disease - a protean disease characterized most commonly by chronic malabsorptive diarrhea, wt loss, migratory non-deforming arthritis, LAD, and low-grade fever
What does infection by protozoan Giardia lamblia cause?
Frothy, foul-smelling steatorrhea due to malabsorption casued by the infecting organism. Not bloody diarrhea
What is cellulitis? What are risk factors? How does it present and waht are the most common infectious agents?
Infection of skin and subcutaenous tissue. Predisopsing - obesity, venous insufficiency, disruption of cutaneous barrier (ex: due to concominent infection, trauma, etc), and previous cellulitis. Presentation: red, edematous skin that is hot to touch. Can also have fever, lymphangitis, and regional LAD. MCC: group A srep and staph aureus
What is MCC of arterial thrombus of popliteal artery?
Atherosclerotic plaque rupture. MC in older pts and presents with acute pain, pallor, paresthesias, pulselessness.
How are DVT and cellulitis different?
Similar fndings of swelling of calf, low-grade fever, erythema, warmth but fever typically doesn't excssed 38.5 in DVT and no regional LAD
What is necrotizing fasciitis and how does it present?
INfection of skin that spreads to fascia. Commonly see skin necrosis, bullae, crepitus, and severe systemic illness
What does a ruptured Baker's cyst cause?
Pseudothrombophlebitis syndrome - swelling seen in posterior calf, just below the knee. Fluid from the cyst may also lead down inner leg, resulting in a hematoma over the medial malleolus known as "crescent sign".
What is Erysipeloid?
Occupational disease caued by ERysipelothrix rhusiopathiae. Typically affects fingers and hands
What is "blue toe syndrome"
Emboli to the pedal circulation cause cyanotic and painful toes with intact pulses - common presentation of catheter-induced atherolmbolism (which results from dislodgement of cholesterol plaques from the aortic root)
What is one of hte more common complcations of cardiac catheterization?
Atheroembolism (.6-1.4%) - dislodged palques may embolize to the cerebral, GI, renal, and cutaneous circulation and cause local iscehmia and organ dysfunction. "blue toe syndrome" results from emboli to small pedal vessels and is characterized by intact pulses and cyanotic toes; can be accompanied by livedo reticularis (the result of ischemic lessions in the lower legs).
Where is distribution of cyanosis from R->L shunts?
toes, fingers and lips (not just one)
What is the most common cause of acute back pain? What is the typical clinical scenario? How manage?
Lumbosacral strain. Typical clinical scenario includes acute onset of the back pain after physical exertion, absence of radiation, presence of paravertebral tenderness, neg straight-leg raising test, and normal neurologic examination. Tx: NSAIDs, early moblization
How does herniated disc present?
Acute pain that radiates to thighs and typically below the knee. Straight leg test positive
How does compression fracture of vertebrae present?
Acute intense pain, local spinal tenderness. Predisposing factors are obvious - post-menopausal or senile osteoporosis, steroid treatment
What are systemic effects of ankylosing spondylitis?
Fatigue, uveitis, pulmonary disase - pulmonary symptoms result form fusion of the costovertebral joints resulting in chest wall motion restriction and restrictive pattern on PFT testing.
What are PFT results in restrictive lung disease?
Both FEV1 and FVC are decreased (<80% predicted), but normal FEV1/FVC (>80%).
What are causes of restrictive lung diseases?
Interstitial lung disease, neuromuscualr disease, alveolar edema, pleural fibrosis, and chest wall abnormalities.
What can cause pulmonary fibrosis?
It is a form of restrictive lung disease - can result from systemic diseases such as RA or scleroderma, cigarette smoking, and meds such as bleomycin. Can also be idiopathic.
How does pulmonary HTN present?
Exertional dyspnea, angina, signs of RHF
What is the most sensitive test for identification of vertebral osteomyelitis?
MRI - excellent for soft tissues and will also reveal whethere there is any abscess or cord compression. Blood cultures are also important for diagnosis bc they allow for directed antibiotic therapy. Bone scan has similar sensitivity to MRI in diagnosis of vertebral osteomyelitis, but ahs inferior specificity - also, doesn't allow for epidrual abscess and SC compression screening
How does vertebral osetomyelitis usually occur and where? What are labs and s/s?
Usually hematogenous. Lumbar area most commonly affected. Back pain accompanied by low-grade feve and elevated ESR is typical presentation. HIgh-grade fever and chills are uncommon. PE: local tenderness on percussion over affected vertebrae and paravertberal muscular spasm. Early dx very important bc epidural abascess and SC compression may develop if treaetment is delayed
Do plain x-rays show acute osteomyelitis?
usually not, but may show chronic.
What is RA?
Chronic, systemic inflammatory disease with progressive erosion of bone and cartilage and significant joint destruction and deformity. Pts typically present with joint findings (ex: pain, stiffness, swelling), morning stiffness, involvement of PIP and MCP joints, and radiologic evidence of erosions and/or periarticular osteopenia.
What are the treatment goals in RA?
Induce and maintain early remission, control synovitis, and prevent progression of joint damage
What is the algorithm for RA treatment?
Start on DMARD (disease modifying antirheumatic agents) ASAP bc joint damage begins early in course. NSAIDs and COX2 inhibitors (ex: celecoxib) are adjunct therapy for symptomatic relief, but don't reduce disease progression. Can also give steroids to relieve symptoms and give short-term radiographic progression, but not effective in preventing joint destruction and can result in generalized bone loss. The DMARDs includ nonbiologics (methotrexate, hydroxychloroquine, sulfasalazine, leflunomide, azathioprine) and biologics (etanercept, infliximab, adalimumab, tocilizumab, rituximab). Methotrexate is the preferred initial DMARD in pts with mod-severe active RA due to its efficacy and long-term safety profile. pts who don't respond to MTX after 6mo may require biologic DMARD such as TNFa inhibitors (etanercept, infliximab) as step-up therapy
What are SE of methotrexate?
Pts should be tested for HEP C and B and TB before starting therapy. Don't use in pts who are pregnant or planning to become pregnant in near future and those with renal insufficiency, liver disease, or excessive alcohol intake.
What is azathioprine and what is its role in RA?
Immunosuppressive. Can be used to treat RA, but not as efficacious as other DMARDs and is assoc with significant hematologic and GI toxicity
What is cyclophosphamide, what is it used for, and what are the seirous SE?
Alkylating agent, used as immunosuppressant in SLE, vasculitis, and certain cancers. In SLE, reserved for pts with significant renal or CNS problems. Many SE - serious ones are acute hemorrhagic cystitis, bladder carcinoma, sterility, and myelosuppression. Hemorrhagic cystitis and bladder cacner are caused by acrolein, a bladder-toxic metabolic of cyclophosphamide. Drinking lots of fluids, voiding freqeuntly, and taking mensa are helpful in preventing these complications
What drugs can casue cochlear dysfunction?
Cisplatin, carboplatin, aminoglycosides
What are cisplatin and carboplatin used to treat?
Testicular, ovarian, and bladder cancers
What drugs cause optic neuritis?
Ethambutol and hydroxychloroquine
What are the toxic causes of peripheral neuropathy?
Phenytoin, Isoniazid, vincristine, heavy metals, chronic alcoholism
What drugs can cause digital vasospasm (Raynauds phenomena)
BB, ergotamine
What durgs can cause thyroid dysfunctoin?
Amiodarone, Lithium
What arhritis can cyclosporine cause?
Gout
What is the main mechanism of kidney damage in SLE pts?
Immune-complex mediated (IC circulate in blood and are deposited in renal glomeruli causing their damage via several mechanisms - one is complement activation -> low C3 in SLE and post-strep (IC-mediated diseases)
What disease has IgE-mediated reaction in kidneys as mechanism for injury?
Allergic interstiital nephritis (ex: methicillin-induced interstitial nephritis)
What is the mechanism of kidney injury in Goodpasture's syndrome?
Cytotoxic Ab
How does anserine bursitis present? Tx?
Sharply localized pain over the anteromedial part of the tibieal plateau just below the joint line of the knee. Valgus stress test fails to reproduce pain, thereby ruling out damage to the MCL. The anserine bursa is located anteromedially over the tibial plateau just below the joint line of the knee. Inflammation can be the result of abnormal jati, overuse, or trauma. Pain often prsent overnight as pressure from the knees making contact with one another while pt lies on their side exacerbates the pain. x-ray is normal. Tx: rest, ice, maneuvers to reduce pressure on bursa. steroid injections into bursa are also helpful.
How does prepatellar bursitis present?
Pain and swelling directly over tibia. Exam: cystic swelling over patella with variable signs of inflammation. MCC: trauma
How does MCL injury present?
Pain along medial joint line, aggravated by walking. Caused by valgus stress applied to lateral aspect of the knee when it is partially flexed. Aggrevated by valgus stress testing
How does medial compartent osteoarthritis present? What does x-ray show?
Pain of medial joint line typically in >40yo. Also have morning stiffness of <30min, crepitus and bony tenderness on exam. X-ray of knee shows narrowing of joint space and osteophyte formation. Can be accompanied by anserine bursitis due to chronic gait abnormality caused by the arthritic pain
How does palletofemoral syndrome present?
Common overuse pain syndrome of knee. Presents with peripatellar pain worsened by activity or prolonged sitting (due to sustained flexion) and may also complain of crepitus with motion of the patella
What are the 2 main causes of avascular necrosis of bone (osteonecrosis)
Chronic steroid use and chornic excessive ingestion of alcohol (>90% combined). Other risk factors: trauma and anti-PL syndrome
What is the pathophys of osteonecrosis (aka aseptic necrosis, avascular necrosis, ischemic necrosis, osteochondritis dessicans)?
Vasculature in affected bone is disrupted causing bone and BM infarction. Subsequently, the bone is unable to remodel and trabecular thinning occurs ultimately leading to collapse of the affected bone. This progression can take months to years to occur.
How do pts with osteonecrosis present? What does immaging show?
Progressive pain. If of femoral head (hip), anterior hip pain worsened by activity and relieved by rest with progressive limitation of range of motion. Progression will ultimately cause joint instability and pain at rest. In forst few months, x-ray will foten fail to show it. MRI is most sensitive test.
When do you see cartilage degeneration in arthritis?
osteoarthritis.
How does aortoiliac occlusion (Leriche) present?
Low back pain, hip, butt, and thigh claudication accompanied by impotence and atrophy of lower extremities. Femoral pulses are weak and bruit may be heard over iliac and femoral arteries
How do pts with SLE present?
Black, 20-40yo, women. Systemic manfestations: fatigue, fever, wt loss, non-deforming arthritis, oral ulers, serositis, hematologic abnormalities (anemia, thrombocytopenia, leukopenia), proteinuria, rash. >90% have arthritis - MC affecting MCP and PIP joints of hands (like RA, but it is non-deforming, unlike RA)
How does dermatomyositis present?
Proximal muscle weakness, rash of shoulders and back, scales on hands.
How does sarcoid present?
Young, black females. Cough, erythema nodosum. AbnL CXR, hyperCa, high ACE level, non-caseating granulomas on bx
Where does neuropathic joint disease most commonly affect?
Feet and ankles
What are systemic effects of hemochromatosis?
Arthropathy of MCP joints, bronzed skin, DM, hepatomegaly, heart failure
Where in hand does DJD often affect?
DIP joints. X-rays: osteophytes, narrowed joint spaces, subchondral bone cysts. Non-inflammatory, no systemic symptoms
How does arthritis of psoriatic arthritis present?
DIP joints mostly. Dactylitis (sausage digit) is characteritisc. Can also see nail pitting and psoriatic plaques
How does PMR present?
Stiffness and pain of shoulders and pelvic girdle. Systemic symptosm fo fever and wt loss are also common.
What does x-ray in RA show?
Joint space erosions, juxta-articular demineralization, and soft tissue swelling
What is the MC cervical radiography finding in cervical spondylosis?
Osteophytes, but specificity is low
What is cervical spondylosis?
affects ~10% of ppl >50yo. History of chronic neck pain is typical. Limited neck rotation and lateral bending due to OA and secondary muscle spasm. Sensory deficit due to osteophyte-induced radiculopathy and isolated sensory abnormalities are assoc with a good prognosis. Typical x-ray findings: bony spurs and sclerotic facet joints. Other findings during cervical spnodylosis may include narrowing of disk spaces and hypertrophic vertebral bodies.
When do you see reversed lordotic curve?
Severe cervical strain
In pt who suspect ankylosing spondylitis by history and PE, what is next step?
Confirm with plain film x-ray (demonstrating fused sacroiliac joints and/or bamboo spine). HLA-B27 testing is nonspecific.
How does AS typically present?
Highest incidence in 2nd-3rd decades of life, M:F 2:1. Should investigate in any young pt with progressive lower back pain and spinal stiffness >3mo duration. Morning stiffness often >30min, typically pain improves with exercise. Dec lumbar spinal mobility and tenderness over sacroiliac joints common. X-ray of sacroliiac joints confirms dx in setting of suggestive history and physical
What is best test for sacroiliitis?
MRI
What is the most common extraarticular manifestation of ankylosing spondylitis?
Anterior uveitis - presents with monocular pain, blurring, photophobia
When do you see positive Anti-DS DNA Ab?
SLE
When do you see glutamic decarboxylase Ab?
Type I DM (70% positive at time of dx)
What Ab are seen in myasthenia gravis?
Acetylcholine receptor Ab
How does chronic fatigue syndrome differ from fibromyalgia?
similar, but in CFS mostly extreme fatigue and not body aches and no trigger points. Need symptoms for >6mo to dx CFS
Does PMR have stiffness, pain, or weakness?
Mostly stiffness rather than weakness or pain
Does polymyositis present with stiffness, weakness, or pain?
Mostly weakness
What is the cause of neurogenic nephroatphy and how does it present? What does X-ray show? How manage?
Aaka Charcot's joint; due to diabetic neuropathy. Starts with dec pain, proprioception, and temperature perception which can occur due to DM, peripheral nerve damage, syringomyelia, spinal cord injury, B12 def, or tabes dorsalis. As normal neurologic input is lots, pts unknowingly traumatize their weight bearing joints -> secondary degenerative joint disease, joint deformation, and functional limitation. X-rays: loss of cartilage, osteophyte development, and loose bodies. Associated pain is typiclaly mild. Management: treat underlying disease nd provide mechanical devices (ex: special shoes) to assist in weight bearing and to dec further trauma.
What do x-rays of chronic gout show?
Punched out erosions with overhanging rim of cortical bone known as a "rat bite" lesion
Where does avascular necrosis commonly affect?
Proximal and distal femur. Pain is hte main symptom
What is the hallmark of osteoporosis?
Bone demineralization -> predisposes to pathologic fracutres, esp in hip and vertebrae, but doesn't itself cause joint destruction
What will x-ray of bacterial arthritis show?
Joint destruction but no osteophytes or loose bodies
What should suspct in lower back pain in pts with history of malignancy?
Bone mets - tumors to bone typically cause constant progressive pain that is worsened at rest, worse at night. MC tumors to mets to bone are lung, breast, prostate, thyroid, kidney
How does lumbar strain present?
usually following twisting of the back while lifting heavy weights. Typically exacerbated by activity and relieved by rest, usually no point tenderness.
How does iliac artery thrombosis present?
Lower back pain assoc with claudication of hip muscles and possibly impotence
What is the classic finding of AS?
Lower back pain that is worse in morning and graually improves through day. Results in progressive limitation of back motion and chest expansion. Assoc findings includ arthritis of peripheral joints and anteior uveitis. X-ray of pelvis: changes in sacroiliac joint consistent with sacroilitis. High ESR, neg RF, +HLA-B27
What is the mechanism of back pain in AS?
Apophyseal joint arthritis
What can cause nerve root demyelination?
Can be caused by many things - including immune-mediated (Guliian-Barre), toxin or med-induced, metabolic, hereditary, or infectious. Cause neurologic abnormalities specific to the affected nerves
What 2 conditions are caused by problems with bone mineralization?
Osteoporosis and osteomalacia - can both present with pathologic fractures
What is MOA of MTX?
Inhibits dihydrofolate reductase
What are SE of methotrexate?
Macrocytic anemia (common), nausea, stomatitis, rash, hepatotoxicity, interstitial lung dsiease, alopecia, fever. Can eventually develp pancytopenia. Shoudl get routine peripheral blood counts q3mo. Can alleviate some of SE with supplemental folic acid without changing efficacy of MTX
What are SE of hydroxycholoquine?
GI disress, visual disturbances, hemolysis in G6PD def
What are SE of cyclosporine?
(used after tx to prevent organ rejection). Predisposes to viral infections and lymphoma and can be nephrotoxic
What are SE of azathioprine?
Pancreatitis, liver toxicity, dose-dependent BM suppression
What causes subacromial bursitis and how does it present? What does PE show?
Result of repetitive overhead motions. Pain with active ROM of shoulder, passive internal rotation and fwd flexion at the shoulder (neer impingement sign) and no signs of deltoid atrophy
How does tear of proximal end of long head of biceps occur and how present?
Assoc with rotator cuff injury and typcailly occurs during forceful flexion of the arm. PE: prominent bulge in midportion of upper arm
What does tennis elbow cause?
Nagging pain over lateral epicondyle
What does palsy of axillary nerve cause?
Paralysis and ultimately denervaion of deltoid and teres minor
What are 3 neuromuscular paraneoplastic syndromes, what are their involved sites, and what are their clinical features?
1. Myasthenia gravis: ACh-R in post-synaptic membrane. Features: fluctuating muscle weakness - ocular (ptosis, diplopia), bulbar (dysphagia, dysarthria), facial, neck, limb muscles. 2. Lambert-Eaton syndrome: Post-synaptic membrane V-gated Ca channels. Features: proximal muscle weakness, autonomic dysfunction (ex: dry mouth), CN involvement (ex: ptosis), DEC/ABSENT DEEP TENDON REFLEXES. 3. Dermatomyositis/ polymyositis: muscle fiber injury. Features: symmetric and more proximal muscle weakness, interstitial lung dsiease, esophageal dysmotility, Raynaud's phenomena, polyarthritis, SKIN FINDINGS in dermato (Grotton's papules, heliotrope rash)
What are paraneoplastic syndromes?
Not related to cancer's invasion - most commonly seen in cancers of lung, breast, ovaries, lymphomas. Symptoms typically reseble those of endocrine, metabolic, hematologic, or neuromuscular disorders
How to dx polymyositis/dermatomyositis?
Muscle bx
In pts with peripheral nerve involvement, what are s/s?
Sensory and/or motor abnormaliteis and abnormal reflexes
How does MG present?
Due to AutoAb against ACH-R in postsynaptic membrane. Flucating ocular (ptosis, diploplia), facial, and/or bulbar muscle weakness that becomes worse with repeititve tasks
How does Lamber-Eaton syndrom present?
Ab targeted against presynatpic membrane (vs MG which is postsynaptic). Can present with proximal muscle weakness, but usually have other autonomic dysufnction (dry mouth, erectile dysf) and absent/diminished deep tendon reflexes. Repeat isometric contraction can lead to temporary improvement of muscle weakness and reappearance of absent DTRs.
How does paraneopalstic myelopathy of SC present?
Flaccid or spastic paraplegia or quadriplegia, sensory deficits, and/or urinary or fecal retention/incontinence
What other bone problems are pts with RA at risk for?
Osteopenia and osteoporosis - most likely due to combined effects of the disease process itself, steroid therapy, female sex, and dec ability to perform weight bearing exercises that prevent osteoporosis
What is osteitis fibrosis cystica? What is the casue?
Aka Von Recklinhausen dsiease of bone. Osteoclastic resorption of bone leads to replacement with fibrous tissue (brown tumors). HyperPTH is the cause
What is the pathophys of paget's disease?
Inc bone turnover due to osteoclastic overactivity leading to replacement of lamellar bone with abnormal woven bone
What is osteomalacia?
Disorder of bone mineralization that causes dec bone density. Vit D def, Ca def, parathyroidectomy and renal tubular acidosis are potential casues
What are risk factors for osteosarcoma in adults?
Primary malignancy bone tumor. Risk factors: chemo and radiation exposure, as well as Pagets disease
Pts with what arthritises are at risk for septic arthritis?
RA, pts with joint damage. Esp at risk for staph aureus
Should you give steroids in septic arthritis?
No due to immunosuppresive action (same with anti-cytokine agents like TNFa inhibitors)
How does allopurinol work?
Inhibits xanthine oxidase -> dec uric acid production
When can absent ankle reflex be normal?
Elderly - as part of normal aging process
How does vertebral compression fracture often occur?
Acute onset of pain, without obvious trauma. It occurs often as a complication of advanced osteoporosis. Local tenderness on PE.
What does absent babinski sign suggest?
No UMN-type lesion
What is Lumbago?
usually related to physical strain and not dramatic onset. Usually have paravertebral rather than spinal tenderness
What type of back pain do you see in multiple myeloma?
Chronic back pain
What is a hand complication of hypothyroidism? What is the pathophys?
Carpal tunnel syndrome (approx 30%). Pathophys: Deposition of mucopolysaccharide protein complexes within the perineurium and endoneurium of the median nerve. In hypothyroid causing carpal tunnel, CTS is commonly BILATERAL and have MORE SEVERE symptoms than other etiologies. Improves wih thyroid therapy
What are clinical features of carpal tunnel?
Nocturnal pain, parestehsia in R medial nerve distribution that are worse with flexion of wrist (positive Phalen test).
What are some causes of carpal tunnel?
Hypothyroid, pregnancy, amyloid fibril deposition (primary and secondary; most common due to amyloid deposition in setting of ESRD or chronic hemodialysis from deposition of beta2 microglobulin), acromegaly (due to soft-tissue enlargement caused by synovial edema and tendon hyperplasia), RA (due to inflammation of tendons and synovial sheath -> inc compartmental pressure)
Why do Baker's cysts develop?
As a result of excessive fluid production by an inflamed synovium - as in cases of RA, OA, and cartilage tears. The excessive fluid accumulates in the popliteal bursa which expands, creating a tender mass in the popliteal fossa. They occasionally burst and release their contents into the calf, resulting in an apperance similar to a DVT.
How does subcutaneous abscess present?
In the setting of folliciulitis or an injury to the skin. Tender, indurated, warm to palpation, erythematous.
What is the cause of lymphedema?
Results from obstruction of lymphatic drainage, as occurs from LN resection or surgical damage to lymphatic vessels.
What is the most serious SE of hydroxychloroquine?
Retinopathy - need eye exams q6mo
How does lateral epicondylitis present?
(tennis elbow). Pain with supination or extension of the wrist and point tenderness just distal to the lateral epicondyle. Results from repeated forceful wrist extension and supination (backhand in tennis, use of screwdriver). Underlying pathophys is degeneration of the extensor carpi radialis brevis tendon near the lateral epicondyle
How does rotator cuff injury present?
Shoulder pain, weakness, dec ROM. Typically result of impingement of supraspinatus tendon
How does radial tunnel syndrome present?
Cuases s/s similar to lateral epicondylitis and may occur with it. Tenderness tends to overly the extensor muscle wad and pain elicited on exma by flexing pt's long finger while acively extending fingers and wrists
How does posterior interosseous nerve entrapment present?
Weakness of extrinsic extensors of hand and fingers.
What should consider in pt with fever and back pain, esp those who are immunosuppressed or IVDA?
Epidural abscess
What is dx TOC for epidural abscess? How treat?
MRI of spine. Tx with abx and surgical decompression. Get blood cx before starting abx
What are epidural abscesses and how do they present? Who is at risk and what are complications?
Enclosed infections of epidural space. Back pain, fever, chills, leukocytosis. Most commonly due to hematogneous spread, tend to occur in IVDA and immunosuppressed. If abscess grows large enough, can cause SC compromised by direct compression and restricted blood flow to the cord -> lower extremity weakness, urinary incontinence.
What is EMG helpful for?
Distinguishing between nerve and muscle disease
Why is LP not used for epidural abscess dx?
Bc of theoretical risk of puncturing the abscess and introducing bacteria into CSF
How do you distinugish gouty arthritis from pseudogout and septic arthritis?
Need synovial fluid analysis - can't do it based on history and exam alone bc all present with acute joint pain, swelling, dec ROM, low-grade fever. Gouty arthritis: WBC of 2,000-50,000 (>50,000 will be septic) with neg gram stain
What are bone scans used for?
metastatic workups and in evaluating suspected fractures or infections
What is arthritis of reactive arhtirits?
Asymmetric oligoarthritis
Is gout monoarticular or poly?
80% mono
What are radiographic findings of hemochromatosis-assoc arthroapthy?
Squared off bone ends and hook-like osteophytes in the 2nd and 3rd MCP joints
What is the gold standard for dx of avascular necrosis of hip? How does it present?
MRI (can have normal x-ray in early stages). Progressive hip or groin pain without restriction of motion.
What is the pathophys of ischemic necrosis of hip?
Ishcemic necrosis of bone with eventual collapse of periarticualr bone and cartilage. Ishcmei bone necrosis is due to compromised blood flow to femoral head that can be truamatic or non-traumatic. Well known causes of non-traumatic avascular (aseptic) necrosis are chronic steroid therapy, alcoholism, and Hb-opathies.
How does septic hip differ from avascular necorsis on presentation?
Avascualr necrosis wont' have dec ROM or fever/chills/erythema (it is aseptic) - just hip pain.
What is De Quervain tenosynovitis?
Condition that affects new mothers who hold their infants with the thumb outstretched (abducted/extended). Abductor pollicis longus and extensor pollicis brevis tendons are affected as they pass through a fibrous sheath at the radial styloid process; passive stretch of these tendons elicits pain (Finkelstein test).
What is trigger thumb?
Results in pain over palmar aspect of 1st MCP joint and locking of the thumb in flexion
How do scaphoid fracutres occur and where is pain?
During forceful hyperextension of wrist often as a result of fall on outstretched hand. Pain typically localizes to the anatomical snuffbox.
What is the presentaiton of flexor carpi radialis tenosynovitis?
Pain with radial flexion of the wrist and point tenderness over the trapezium
How does psoriatic arthritis present? How tx?
DIP joints. Morning stiffness, deformity, dactylititis (sausage digit), and nail involvement. NSAIDs, anti-TNFa agents, and MTX. Systemic steroids are contraindicated.
What are classic skin lesions of psoriasis?
Well demarkated red plaques with silvery scaling
How common is enteropathic arthritis in IBD? How does it present?
10-20%. Affects lower extremities and sacroiliac joints and tends to wax and wane with symptoms of IBD.
Where do tophi occur?
over joints and helix of the ear. They can ulcerate
When do you see polyarthritis affecting the ankles and knees?
Sarcoidosis.
What joint is most commonly affected in hand in OA?
DIP. Worse with activity, better with rest. Noninflammatory
How should you treat OA?
Acetaminophen for mild-moderate (NSAIDs have SE that make them second line -just used for exacerbations)
What valvular problem are pts with AS at risk for?
AR secondary to scarring of arotic valve cusps
What conditions are thoracic artoci aneurysms assoc with?
Marfans, Ehlers-Danlos, Syphillis
What conditions are oral ulcers assoc with?
SLE, Crohns, Behcets disease
What is a feared complication of temporal arteritis?
Ischemic optic neruopathy - results from vasculiitis of the retinal artery and may cause blindness
What is Episcleritis assoc with?
RA and IBD
What kidney problems can you get with AS?
Secondary amyloidosis and IgA nephropathy but rare and only occasionally lead to renal failure
What are the Ca, P, alk phos, and urinary hydroxyproline changes in pagets (osteitis deformans)?
Normal Ca, P. Inc alk phos and urinary hydroxyproline levels (as well as other elevated urinary markers of bone degradation such ad exoysyridinoline, N-telopeptide, C-telopeptide
What are the changes in Ca, P, alk phos in hyper PTH?
High Ca, low P, high alk phos
When will you see high Ca with normal phosphate and alk phos?
Milk-alkali syndrome
What is whipple disease, what causes it, what is presentaiotn and how diagnose?
Most commonly presents wtih chronic malabsorptive diarrhea (steatorrhea, flatuence, abd distention), protein-losing enteropathy, wt loss, migratory non-deforming arthritis, LAD, low-grade fever. Can also damage eye, CNS, and myocardium. Caused by infection with gram+ bacillus Tropheryma whippelii. Dx: small intestinal bx and PCR - bx shows PAS-positive macrophages in the lamina propria containing non-acid-fast gram + bascilli
What does UC look like on bx? Crohns?
UC: Acute and chronic inflammation of the mucosa leading to crypt abscess formation. Crohns: full-thickness inflammation with granuloma and lymphoid aggreate formation and skip lesions
How does intestinal lymphoma present?
Abd pain, wt loss, N/V, distention, occult blood in stool. Histology: diffuse infiltrate by atypical lymphocytes
What happens in HIV with MAI infects small intestinal wall?
fever, malabsorptive diarrhea, weight loss. PAS+ macrophages on bx, but unlike whipples, bacilli are acid fast
What happens in chronic tophaceous gout? What is ddx?
Urate crystals can be deposited in the skin resulting in the formation of tumors with a chalky white appearance. Ddx of tophi: rheumatoid nodules, calcinosis cutis
How does inc uric acid lead to nephrolithiasis?
Uric acid crystals form in renal tubules and collecting systems
How do thiazides inc risk of gout?
hyperuricemic effect resulting from hypovolemia-assoc enhancement of uric acid reabsorption in the proximal tubule
What do rheumatoid nodules look like?
Classicaly, they are firm, flesh-colored and non-tender. Occur over pressure points such as elbow and extensor surfaces of the proximal ulna.
What nodes can you get in severe OA?
Heberden and Bouchard nodes - hard, bony nodules over the distal and proximal interphalangeal joints, respectively
When do vertebral comrpression fracturs occur?
Almost always occur when bone demineralization is present. This occurs in osteomalacia, where inadequate serum Vit D, Ca, or P results in demineralized osteoid. It also occurs in osteoporosis, a condition where bone mineral density is decreased and the bone's microarchitecture is disrupted. Pathologic fractures can occur in either condition
How do ligamentous sprains of the back present?
Often can be traced to a specific event or action. More painful with movement, feel best in the morning. Pain is perispinal, not on bone
When do you see lumbar disk degeneration?
Hallmark of lumbar OA. Presents as low back pain in elderly. Worsens as day progresses, relieved with rest.
When do you see apophyseal joint arthritis?
Hallmark of ankylosing spondylitis. Pain and progressive limitation of back motion. Worse in morning, improves throughout the day (like RA)
When can you see nerve root demyelination?
Many things - including immune-mediated (Gullian-Barre), toxin or med-induced, metabolic, hereditary, or infectious. WIll have neuro abnormaltieis that correspond to the affective nerve roots. no back pain or tenderness to palpation
How do you treat reactive arthritis?
NSAIDs are first line. Don't need abx.
What is the classic triad of reactive arthritis?
Nongonococcal urethritis, asymmetric oligoarthritis, and ocnjunctivities. In addition, mucocutaneous lesions and ethesitis (Achilles tendon pain) are common findings in reactive arthritis. Becuase not all symptoms are always present, there should be high suspicion for reactive arthritis in case of any asymmetric oligoarthritis assoc with urethritis, conjunciviits, or mouth ulcers. Synoival fluid is usually sterile
What is chondriotin sulfate used for?
Many pts with OA take it - it is a component of the ground substance that composes cartilage . But not definitively shown to help
What does Parvovirus B19 cause in terms of arthritis and how dx?
Arthritis of MCP, PIP, wrist and ankle joints. Anti-B19 IgM is dx TOC when clinically suspected. Adults working with kids are at inc risk. Adults often dont' have slapped cheek appearance. Symptoms resolve within 2mo. Ab develop 10-15d after infection and usually remain positive for 1-6mo
What are common casues of viral arthritis?
Parvovirus, hepatitis, HIV, rubella
What Ab factors are assoc with RA?
RF, anti-CCP
How long must sypmtoms be present to be able to dx RA?
6mo
What tests can you do for SLE?
ANA highly sensitive, anti-ds DNA highly specific
What are ASO titers used for and what will you see on exam?
Recent strep infection, + in acute rheumatic fever (migratory polyarthritis (usually lower extremities first), carditis, chorea, erythema marginatum, subcutaneous nodules)
What type of arthritis does hyperPTH predipose to?
Pseudogout
What are s/s of hyperCa?
Consptiation, fatigue, excssive urination, abd pain, urinary stones, AMS, osteoporosis
What do struvite crystals look like and when do you see them?
Shape of coffin lids. Seen in kidney stones caused by chornic UTI with urease-producing organisms
How does fungal arthritis usually present and how common is it?
Rare. Monoarthritis of the knee.
What is Enthesitis?
Condition in which inflammation and pain occur at the site of tendon and ligament attachment to bone and is acommon finding in ankylosing spondylitis. Typical sites: heels, tibial tuberosities, iliac crests.
What hand deformities do you see in RA?
Ulnar deivation of fingers, swan-neck deformities, boutonniere deformities.
When do you see subcutaneous nodules in arthritis?
RA, gout. Tend to be painless, slow growing, cocur at pressure points such as olecranon process.
How can you help prevent lumbar back strain (relation to lifitn a heavy object, no radicular signs, good response to conservative therapy)?
Proper pt education - ex: teaching the proper techniques for bending and lifting objects. Also, strenghtneing muslces with regular exercise, good sleeping posture (dont' sleep on back), dont' do exercises with repetitive twisting and bending. Warm up before exercising
What is CREST syndrome?
Constellation of findings including Calcinosis cutis, Raynaud phenomenon, Esophageal dysmotlitiy, Sclerodactyly, and Telangiectasias. It is a limited form of systemic sclerosis. Calcinosis cutis: localized dysrophic depoisiton of Ca in the skin and manifests as pink-to-white noduels typically on the upper extremities - can ulcerate and drain chalking maternal. Raynaud phenom: acute bouts of digial ischemia in response to cold, may lead to digial necrosis; fingers typically progress thru white, blue, and hyperemic stages. Esophagel dysmoitlity - classically dysphagia and GERD. Sclerodactyly: fibrosis of the skin of the fingers distal t the MCP joitns resulting in a shiny apperance of the skin and flexion contractures and joint pain. Telangiectasias: "mat-like" patches most commonly on face and palms
What type of dysphagia does achalasia cause?
both solids and liquids. Barium esophagogram: "birds beak" sign in the distal esophagus
How does diffuse esophageal spasm present?
Acute and severe retrosternal pain as well as dysphagia due to uncoordinated and/or hypertensive esopahgeal contractions
What is Felty syndrome?
Splenomegaly with neutorpenia (<2,000) in RA. Granulocytopenia doesnt' occur until symptoms of arthritis have been present for >10yrs. Note: splenomegaly is a common finding in pts with RA without granulocytopenia (not felty's)
What are systemic symptoms of RA?
Rheumatoid nodules, pulmonary fibrosis and infiltrate, scleritis, and rarely splenomegaly with neutropenia (Felty syndrome)
What are common SE of methotrexate?
Hepatotoxicity, stomatitis, nausea, abd pain, fever, myelosuppresion
How does acute hepatitis present?
Dramatic increases in ALT and AST, jaundice, viral prodrome of fever, malaise, N/V
What are SE of steroid treatment?
Thinning of skin, immunosuppression, hyperglycemia, gastritis, psychosis.
What are SE of anti-cytokine agents such as infliximab, etanercept, and adalimumab?
Rare SE: predisposition to infection, cytopenia, development of lymphomas
How can you help to prevent SE of MTX?
Give folic acid (doesn't interfere with effectiveness of MTX)
What are the 6 criteria used to establish the diagnosis of OA in the setting of a painful knee?
Age >50, bony enlargement, bony tenderness, crepitus, lack of warmth/morning stiffness. If 3+ criteria are met, specificity for OA is 69%
Where is OA most common in body?
Knee, hip, spine, fingers. Often monoarticular
How helpful is uric acid level?
Nonspecific
What does pain at site of tibial tuberosity indicated?
Enthesiits - inflmmation at site of tendon insertion into bone, occurs in spondyloarthropathies such as AS
What pts get Bakers cyst (palpable popliteal mass)?
RA
When do you see rotator cuff tendonitis?
Caused by impingement. Most common in middle-aged older pts who perform repetitive arm movements above the head. Presents with pain when lifting arm. Confirmed by Neer test (passive motion above the head causes pain and guarding) - confirms dx
How can differentiate rotator cuff tendonitis/impingement from rotator cuff tear and frozen shoulder?
Isoalted rotator cuff tendonitis symptoms (dec ROM, pain) will be relieved with injection of lidocaine
How do you definitivley dx rotator cuff tendonitis/impingement?
MRI
How can you get rotator cuff tear. S/S
Trauma (ralling on outstretched arm) or as a result of chronic impingement and tendonitis. Often complain of pain reaching and lifting arm over head. Weakness more common in tear than in rotator cuff tendoniitis/impingement. Symptoms don't resolve with lidocaine injeciton (but do with impingement)
What is adhesive capsulitis (Frozen Shoulder)?
Idiopathic condition of pain and contracture. Presents with inability to lift arm above head. Not improved with lidocaine injection
How does cervical radiculopathy present?
Pain of neck and arms. Paresthesia of arm present in 80% of patients. Can have weakness of shoulder, elbow, or wrist depending on the cervical roots involved. Movement exacerbates the symptoms.
How can you get vascular compression of upper extremities and how does it present?
May occur in thoracic outlet syndrome. Most commonly presents with a combo of numbness, weakness, swelling due to compression of the subclavian vessels and lower trunk of the brachial plexus. A weakened radial pulse and reproduction of symptoms with specific arm movements supports the diagnosis.
How does dissemintate gonococcemia present?
High fever, chills, tenosynovitis, migratory polyarthralgias, and a small number of pustular lesions on the extremities. Routine blood and pustule cultures are typically negative due to teh growth requirements of the organism. Skin lesions are discrete purpuric or pustular lesions with a hemorrhagic component and occasionally central necrosis.
What is the MCC of infective endocarditis in IVDA?
Staph auresu
How do pts with TSS present?
Fever, erythroderma/desquamatoin, headache, N/V, myalgias. Blood cultures are neg bc it is a toxin-mediated illness
What are the cutaneous manifestations of acute HIV syndrome?
Like those of other viral examthems - namely, morbilliform macules.
What are the cutaneous manifestations of secondary syphilis?
Morbilliform, psoriasiform, or pustular. Condylomata lata typically in anogenital region. Fever, arthralgias.
What is the MCC of spinal stenosis?
Vertebral DJD
How do you dx and treat spinal stenosis?
Dx: MRI. Tx: conservative or surgical (laminectomy)
How does spinal cord compression as a cause of lower back pain present?
Back pain, paralysis, hyperreflexia, urinary and fecal incontninence or urinary retention