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1.
Am Fam Physician ; 84(11): 1245-52, 2011 Dec 01.
Article in English | MEDLINE | ID: mdl-22150658

ABSTRACT

Rheumatoid arthritis is the most commonly diagnosed systemic inflammatory arthritis. Women, smokers, and those with a family history of the disease are most often affected. Criteria for diagnosis include having at least one joint with definite swelling that is not explained by another disease. The likelihood of a rheumatoid arthritis diagnosis increases with the number of small joints involved. In a patient with inflammatory arthritis, the presence of a rheumatoid factor or anti-citrullinated protein antibody, or elevated C-reactive protein level or erythrocyte sedimentation rate suggests a diagnosis of rheumatoid arthritis. Initial laboratory evaluation should also include complete blood count with differential and assessment of renal and hepatic function. Patients taking biologic agents should be tested for hepatitis B, hepatitis C, and tuberculosis. Earlier diagnosis of rheumatoid arthritis allows for earlier treatment with disease-modifying antirheumatic agents. Combinations of medications are often used to control the disease. Methotrexate is typically the first-line drug for rheumatoid arthritis. Biologic agents, such as tumor necrosis factor inhibitors, are generally considered second-line agents or can be added for dual therapy. The goals of treatment include minimization of joint pain and swelling, prevention of radiographic damage and visible deformity, and continuation of work and personal activities. Joint replacement is indicated for patients with severe joint damage whose symptoms are poorly controlled by medical management.


Subject(s)
Arthritis, Rheumatoid , Antirheumatic Agents/therapeutic use , Arthritis, Rheumatoid/diagnosis , Arthritis, Rheumatoid/drug therapy , Arthritis, Rheumatoid/etiology , Combined Modality Therapy , Complementary Therapies , Diagnosis, Differential , Exercise Therapy , Humans , Prognosis , Risk Factors
2.
J Clin Rheumatol ; 15(8): 383-6, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19955993

ABSTRACT

Patients with systemic lupus erythematosus (SLE) commonly have vasculitis with cutaneous involvement. Disease activity associated with SLE is frequently responsible for the vasculitis, although infection is also important to consider. We describe a young woman with SLE who was found to have leukocytoclastic vasculitis due to Candida albicans.


Subject(s)
Candidiasis/complications , Fungemia/complications , Lupus Erythematosus, Systemic/complications , Vasculitis, Leukocytoclastic, Cutaneous/microbiology , Adult , Female , Humans
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