Literature DB >> 8907065

Adult immunodeficiency and rheumatic disease.

S Itescu1.   

Abstract

Several rheumatic illnesses may develop in adults with primary or acquired immunologic defects. Individuals with primary defects in B-cell antibody production, such as common variable immunodeficiency of selective IgA deficiency, and those with defects of complement components, have an increased prevalence of systemic lupus erythematosus--like syndromes or other autoimmune diseases. Defects in immunoglobulin production may be complicated by inflammatory or infectious arthritis. Infection with HIV-1 may be associated with diverse rheumatic conditions, including diffuse infiltrative lymphocytosis syndrome, myopathies, vasculitides, inflammatory arthritides, and infectious musculoskeletal complications. An approach to these disorders that takes into consideration the underlying mechanism of disease is presented. Appropriate strategies aimed at treatment of the underlying immunodeficiency may improve the clinical course of the associated rheumatic disorder.

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Year:  1996        PMID: 8907065     DOI: 10.1016/s0889-857x(05)70262-3

Source DB:  PubMed          Journal:  Rheum Dis Clin North Am        ISSN: 0889-857X            Impact factor:   2.670


  1 in total

1.  Selective immunoglobulin A deficiency and primary antiphospholipid syndrome.

Authors:  Antonio G Tristano
Journal:  Rheumatol Int       Date:  2005-01-15       Impact factor: 2.631

  1 in total

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