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113 Cards in this Set
- Front
- Back
Connective tissue disease (CTD) |
is the major focus of rheu-matology, the study of rheumatic disease |
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rheumatic disease |
is any disease or condition involving the musculoskeletal system. |
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Arthritis |
means inflammation of one or more joints. In clini- cal practice, however, arthritis is categorized as either nonin- flammatory or inflammatory. |
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Osteoarthritis |
-Noninflammatory, localizedarthritis - the progressive deterioration and lossof cartilage in one or more joints (articular cartilage) |
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osteophytes |
(bone spurs) |
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crepitus |
a grating sound caused by the loosened bone and cartilage. |
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primary OA |
the disease may be triggered byaging, genetic changes, obesity, and/or smoking. |
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Secondary OA |
occurs less often than primary disease and can result from other musculoskeletal conditions, such as rheumatoid arthritis. |
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OA pain assessment in detail. Other questions to ask include: |
-If joint stiffness has occurred, where and for how long? -When and where has any joint swelling occurred? -What do you do to control the pain or stiffness? -Do you have any loss of function or difficulty in per- forming ADLs? |
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Heberden’s nodes |
(at the distal interphalangeal [DIP] joints) |
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Bouchard’s nodes |
(at the proximal interphalangeal [PIP] joints) |
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Joint effusions |
(excess joint fluid) are common when the knees are involved. |
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infrapatellar notch |
(the area directly below the knee) |
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suprapatellar area |
(directly above the knee). |
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OA Disease pattern |
-May be unilateral, single joint -Affects weight-bearing joints and hands, spine ---Metacarpophalangeal joints spared -Nonsystemic |
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OA Disease process |
Degenerative |
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OA LAB FINDINGS |
Normal or slightly elevated ESR |
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OA Common drug therapy |
NSAIDs (short-term use) Acetaminophen Other analgesics |
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OA typical onset age |
older than 60yrs |
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OA Risk Factors or cause |
-Aging -Genetic factor (possible) -Obesity -Trauma -Occupation |
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OA- Local rest |
involves immobilizing any unstable joint, most often the knee, with a brace or splint |
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OA Systemic rest |
refers to immobilizing the entire body, such as during a nap. |
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OA Psychological rest |
is equally important because it allows relief from the daily stresses that can enhance pain. |
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Glucosamine |
may decrease inflammation |
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chondroitin |
may play a role in strengthening cartilage. |
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totaljoint arthroplasty (TJA) |
-surgical creation of a joint -The most common surgical procedure performed for older adults with OA -aka total joint replacement (TJR ) |
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osteotomy |
(bone resection) may be performed to correct joint deformity, but this procedure is done most commonly for younger adults |
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Osteonecrosis |
is bony necrosis secondary to lack of blood flow, usually from trauma or chronic steroid therapy. |
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primary arthroplasty. |
The first time a patient receives any total joint arthroplasty, it is referred to as |
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revision arthroplasty |
If the implant loosens, _______may be performed. |
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neuroaxial |
(epidural/spinal) anesthesia for LOWER EXTREMITY SURGERY |
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subluxation |
-(partial dislocation) or total dislocation. -A major complication of THA(total hip arthroplasty) |
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peripheral nerve blockade (PNB) |
One of the most recent advances in postoperative painmanagement for lower extremity total joint arthroplasty (TJA or TJR) - the anesthesiologist injects the femoral or sciatic nerve with localanesthetic; the patient may receive a continuous infusion ofthe anesthetic by portable pump. |
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hemiarthroplasty |
replacement of part of the joint), typically the humeral component, may be performed as an alternative to TSA ( TOTAL SHOULDER ARTHROPLASTY) |
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Recreational exercise |
includes hobbies and sports, with no planned purpose other than relaxation. |
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Therapeutic exercise |
-includes carefully planned activities that are designed to improve muscle strength, muscle tone, and joint range of motion. -can also reduce pain and improve the patient’s psy- chological health. |
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Rheumatoid arthritis (RA) |
is a common connective tissue disease that can be the most destructive to the joints |
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Systemic |
means this disease affects the body system, affecting many joints and other tissues. |
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pannus |
is vascular granulation tissue composed of inflammatory cells; it erodes articular cartilage and eventually destroys bone. |
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vasculitis |
If blood vessel involvement occurs, the organ supplied by that vessel can be affected. -The result is malfunction and eventual failure of the organ or system |
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migratory arthritis. |
In early disease, the patient may report migrating symptoms known as |
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gel phenomenon |
The patient usually has frequent morning stiffness ......which lasts for 45 minutes to several hours after awakening. |
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effusions |
(joint swelling with fluid, especially the knees). -On palpation, the joints feel soft and look puffy because of synovitis and |
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Baker’s cysts |
(enlarged popliteal bursae behind the knee) |
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periungual lesions |
Assess for ischemic skinlesions that appear in groups as small, brownish spots, most commonly around the nail bed |
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paresthesias |
-burning and tingling sensation, -Peripheralneuropathy associated with decreased circulation can causefootdrop and ____ usually in older adults. |
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Sjögren’s syndrome (RA) |
which includes a triad of: -Dry eyes (keratoconjunctivitis sicca [KCS], or the sicca syndrome) -Dry mouth (xerostomia) -Dry vagina (in some cases) |
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Felty’s syndrome (RA) |
hepatosplenomegaly (enlarged liver and spleen), and leukopenia |
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Caplan’s syndrome (RA) |
is characterized by the presence of rheumatoid nodules in the lungs and pneumoconiosis, which is noted primarily in coal miners and asbestos removal workers. |
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synovectomy |
to remove inflamed synovium may be needed for joints like the knee orelbow. |
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disease-modifying antirheumatic drugs (DMARDs) |
-most patients are managed with -As the name implies, thesedrugs are given to slow the progression of the disease (RA) |
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Methotrexate(MTX) (Rheumatrex) |
-Patients taking MTX are at risk for infection. -Teach themto avoid crowds and people who are ill. -Remind patients to avoidalcoholic beverages while taking MTX to prevent liver toxicity. -Teach them to observe and report other side and toxic effects,which include mouth sores and acute dyspnea from pneumoni-tis - Strict birth control is recom-mended for childbearing women who are in need of MTX tocontrol their RA |
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Leflunomide (Arava) |
- Teach patients to report these changes and monitor laboratoryresults carefully. -Remind them to avoid alcohol. -Inform themthat Arava can cause birth defects, and therefore recommendstrict birth control to women of childbearing age. -Tell patientsto contact the health care provider immediately if pregnancyoccurs while taking the drug. -Cholestyramine (Questran) isavailable to help block the drug’s action. |
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Nonsteroidal Anti-inflammatory Drugs. NSAIDs |
aresometimes used for inflammatory arthritis to relieve pain andinflammation |
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Plasmapheresis |
(sometimes called plasma exchange) is an in-hospital procedure prescribed by a health care provider in which the patient’s plasma is treated to remove the antibodies causing the disease |
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energy conservation |
including: - Pacing activities - Allowing rest periods - Setting priorities - Obtaining assistance when needed |
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RA typical age |
35-45 years |
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RA risk factors or cause |
- Autoimmune (genetic basis) -Emotional stress (triggers exacerbation) -Environmental factors |
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RA Disease process |
Inflammatory |
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RA Disease pattern |
-Bilateral, symmetric, multiple joints -Usually affects upper extremities first -Distal interphalangeal joints of hands spared -Systemic |
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RA Lab findings |
-Elevated rheumatoid factor -antinuclearantibody -ESR |
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RA common drug therapy |
-NSAIDs (short-term use) -MethotrexateLeflunomide (Arava) -Corticosteroids -Biological response modifiers -Other immunosuppressive agents |
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The two main classifications of lupus are |
-discoid lupuserythematosus (DLE) - systemic lupus erythematosus(SLE) |
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systemic lupus erythematosus (SLE) |
is a chronic,progressive, inflammatory connective tissue disorder that cancause major body organs and systems to fail. -characterized by spontaneous remissions and exacerbations (“flare-ups”), and the onset may be acute or insidious (slow). - condition is potentially fatal, but the survival rate hasimproved dramatically when SLE is diagnosed early andtreated adequately |
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lupusnephritis (SLE) |
- some degree of kidney involvement—the leading cause of death. -Autoimmune complexes in SLE tend to be most attractedto the glomeruli of the kidneys. -Other causes of deathfrom the disease are cardiac and central nervous systeminvolvement. |
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Lupus caused by |
Like RA, lupus is probably caused by a combination of genetic and environmental factors. |
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“butterfly”rash |
The major skin manifestation of DLEand SLE is a dry, scaly, raised rash on the face |
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discoid lesions |
-(coinlike) the scarring lesions of discoid lupus. The lesions are especially evidentwhen the patient is exposed to sunlight or ultraviolet light. |
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Osteonecrosis |
(bone necrosis from lack of oxygen)is often seen in those who have been treated for at least 5 yearswith steroids like prednisone |
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myositis |
Observe for muscle atrophy, which can result from disuse,from skeletal muscle invasion by the immune complexes or from chronic steroid therapy |
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Myalgia |
(muscle pain) |
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Pericarditis |
is the most common cardiovascular manifesta-tion and causes tachycardia, chest pain, and myocardial ischemia. |
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Raynaud’s phenomenon |
occurs in a small portion of lupuspatients. On exposure to cold or extreme stress, the patientreports the characteristic red, white, and blue color changesand severe pain in the digits; these changes are caused byarteriolar vasospasm. |
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serositis |
(peritoneal involvement) - Mesenteric arteritis, pancreatitis from arteritis of the pancreatic artery, and colonic ulcersalso can cause abdominal pain with lupus. |
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pancytopenia |
(a decrease of all cell types) |
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hydroxychloroquine (Plaquenil) (SLE) |
- decreases the absorption of ultraviolet lightby the skin and therefore decreases the risk for skin lesions. -Teach patients to have frequent eye examinations if they arereceiving _______ |
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discoid lupus erythematosus (DLE) the patient’s major concern |
is the rash or discoid lesions |
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Systemic sclerosis (SSc) |
-also called scleroderma -is an uncommon chronic, inflammatory, autoimmune connective tissue disease. -Formerly called progressive systemic disease, or PSS, this illness is not always progressive. |
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Scleroderma |
means hardening of the skin, which is only one clinical manifestation of the problem. -Some patients, often children, have only skin involvement, or localized scleroderma (also called linear scleroderma) |
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sclerotic |
The inflamed tissue in patients with SSc be comes fibrotic and ____ (hard) |
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two classification for systemic sclerosis |
-Diffuse cutaneous SSc—skin thickening on the trunk, face, and proximal and distal extremities (over most of the body) - Limited cutaneous SSc—thickened skin limited to sites distal to the face, neck, and distal extremities |
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Patients with the limited form of systemic sclerosis often have the CREST syndrome |
-Calcinosis (calcium deposits) -Raynaud’s phenomenon (1st symptom that ocurs) -Esophageal dysmotility -Sclerodactyly (scleroderma of the digits) -Telangiectasia (spider-like hemangiomas) The first symptom that usually occurs in patients with the diffuse form of the disease is hand and forearm edema, which may exist with bilateral carpal tunnel syndrome. |
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Arthralgia |
(joint pain) |
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indurative phase |
In this phase, the fingers are described as sausage-like. The skin is taut, shiny, and free of wrinkles. If diffusescleroderma occurs, swelling is replaced by tightening, hard-ening, and thickening of skin tissue |
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autoamputation |
(the tips of the digits fall off spontaneously) |
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Gout, or gouty arthritis |
is a systemic disease in which urate crystals deposit in the joints and other body tissues, causing inflammation |
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Primary gout |
is the most common type and results from one of several inborn errors of purine metabolism. |
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Secondary gout |
involves hyperuricemia (excessive uric acid in the blood) caused by another disease or factor. Sec- ondary gout affects people of all ages |
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three clinical stages of the primary disease process of gout |
asymptomatic hyperuricemia, acute gouty arthritis chronic or tophaceous gout |
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asymptomatic hyperuricemia |
- patient is usually unaware - The serum uric acid level is elevated, but no treatment is needed in this stage |
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acute gouty arthritis |
- The patient experiences excruciating pain and inflammationin one or more small joints, usually the metatarsophalangealjoint of the great toe, called podagra. -The erythrocyte sedimentation rate (ESR) is usually increased as a result of theinflammatory process. -- Joint inflammation is the most common finding and is usually so painful that the patient seeks medical care immedi- ately. |
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chronic or tophaceous gout |
-uratekidney stone formation is more common than renal insufficiency. - can begin anywhere between 3 and40 years after the initial gout symptoms occur - inspect the skin for tophi, or deposits ofsodium urate crystals |
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Polymyositis |
is a diffuse inflammatory disease of skeletal (striated) muscle that causes symmetric weakness and atrophy. |
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dermatomyositis |
When a rash accompanies polymyositis, the diseaseis called |
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polyarthralgia |
(aching around multiple joints), |
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Necrotizing vasculitis |
is a term for a group of diseases whose primary manifestation is arteritis (inflammation of arterial walls), which causes ischemia in the tissues usually supplied by the involved vessels |
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Polyarteritis nodosa |
affects middle-aged men most oftenand involves every body system. Treatment is similar tothat for systemic lupus, but the prognosis is not as promis-ing. Renal disorders and cardiac involvement are the mostcommon causes of death |
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Hypersensitivity vasculitis |
is the most common form of vasculitis and primarily causes skin lesions as an allergic response to drugs, infections, or tumors. |
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Takayasu’s arteritis |
or the aortic arch syndrome, is also called the “pulseless” disease |
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Polymyalgia rheumatica (PMR) |
is a clinical syndrome characterized by stiffness, weakness, and aching of the proximal musculature (i.e., the shoulder and pelvic girdles). |
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Giant cell arteritis (GCA) |
-or temporal arteritis (TA), occurs in as many as 20% of people with PMR. -GCA is a systemic vasculitis that affects large and midsize arteries - the cause of both PMR and GCA is unknown, but a geneticpredisposition related to HLA-DRB1 is likely. - GCA istreated urgently with high doses of corticosteroids, often ashigh as 40 to 80 mg daily |
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Ankylosing spondylitis (AS) |
s also known as Marie-Strüm-pell disease or rheumatoid spondylitis. -The disease affects thevertebral column and causes spinal deformities. - Other features include: iritis (inflamma-tion of the iris), arthritis or arthralgia (joint aching), andnonspecific systemic manifestations such as malaise andweight loss. |
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Reiter’s Syndrome |
- As with ankylosing spondylitis, Reiter’s syndrome is associatedwith the HLA-B27 antigen. -This disease usually affects youngwhite men but can also affect women. |
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balanitis circinata |
(ringlike inflammation of the glans penis) |
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Marfan syndrome |
is an autosomal dominant connective tissue disease in which abnormalities of the skeletal, ocular, cardiopulmonary, and central nervous systems result from a basic defect in extracellular microfibrils. Microfibrils are very small fibers within cells. - tend tobe excessively tall and have elongated hands and feet. - Cardiovascular problems are responsible for most deathsresulting from ______ |
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Infectious Arthritis |
Any infectious agent can invade the joint space and causeinflammation and tissue destruction. |
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Lyme disease |
is a reportable systemic infectious diseasecaused by the spirochete Borrelia burgdorferi and results fromthe bite of an infected deer tick, also known as the black-legged tick. |
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erythema migrans |
round or oval, flat orslightly raised rash |
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Pseudogout |
is a disease that mimics the clinical manifesta- tions of gout. |
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Psoriatic arthritis (PsA) |
affects about 30% of people who have psoriasis—a skin condition characterized by a scaly, itchy rash, usually on the elbows, knees, and scalp |
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Fibromyalgia syndrome (FMS) |
also referred to as simplyfibromyalgia, is a chronic pain syndrome, not an inflamma-tory disease. |
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trigger points (FMS) |
-can typically be palpated to elicit pain in a predictable, reproducible pattern. -The pain is typically described as burningand gnawing. |
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Chronic fatigue syndrome (CFS), |
also known as chronic fatigue and immune dysfunction syndrome (CFIDS), - is a chronic illness in which patients have severe fatigue for 6 months or longer, usually following flu-like symptoms. |