Systemic lupus erythematosus
Identifieur interne : 002A18 ( Main/Exploration ); précédent : 002A17; suivant : 002A19Systemic lupus erythematosus
Auteurs :Source :
- Drug and Therapeutics Bulletin [ 0012-6543 ] ; 1996-03.
English descriptors
- Teeft :
- Antiphospholipid, Antiphospholipid syndrome, Arthritis rheum, Azathioprine, Blood pressure, Clinical features, Coronary artery disease, Corticosteroid, Cyclophosphamide, Cytotoxic, Cytotoxic drugs, Disease activity, Dos, Erythematosus, Haemolytic anaemia, Hydroxychloroquine, Inflammation, Intravenous, Intravenous cyclophosphamide, Lupus, Lupus erythematosus, Lupus nephritis, Mild disease, Neonatal lupus syndrome, Nephritis, Nsaid, Oral cyclophosphamide, Organ involvement, Prednisolone, Prednisolone dose, Pulse cyclophosphamide, Rash, Regimen, Remission, Renal, Renal failure, Renal function, Rheum, Severe inflammation, Severe lupus nephritis, Severe nephritis, Spontaneous abortion, Subacute cutaneous lupus erythematosus, Syndrome, Systemic, Systemic lupus erythematosus, Vital organs.
Abstract
It has been estimated that about 3 in 10 000 people in Britain's cities have systemic lupus erythematosus (SLE)1 and the true figure may be higher.2 Forty years ago, approximately 50% of patients with SLE died within 4 years of diagnosis.3 Prospects have improved with refinements in therapy and the recognition of mild forms of the disease.
Url:
DOI: 10.1136/dtb.1996.34320
Affiliations:
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Le document en format XML
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<profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Antiphospholipid</term>
<term>Antiphospholipid syndrome</term>
<term>Arthritis rheum</term>
<term>Azathioprine</term>
<term>Blood pressure</term>
<term>Clinical features</term>
<term>Coronary artery disease</term>
<term>Corticosteroid</term>
<term>Cyclophosphamide</term>
<term>Cytotoxic</term>
<term>Cytotoxic drugs</term>
<term>Disease activity</term>
<term>Dos</term>
<term>Erythematosus</term>
<term>Haemolytic anaemia</term>
<term>Hydroxychloroquine</term>
<term>Inflammation</term>
<term>Intravenous</term>
<term>Intravenous cyclophosphamide</term>
<term>Lupus</term>
<term>Lupus erythematosus</term>
<term>Lupus nephritis</term>
<term>Mild disease</term>
<term>Neonatal lupus syndrome</term>
<term>Nephritis</term>
<term>Nsaid</term>
<term>Oral cyclophosphamide</term>
<term>Organ involvement</term>
<term>Prednisolone</term>
<term>Prednisolone dose</term>
<term>Pulse cyclophosphamide</term>
<term>Rash</term>
<term>Regimen</term>
<term>Remission</term>
<term>Renal</term>
<term>Renal failure</term>
<term>Renal function</term>
<term>Rheum</term>
<term>Severe inflammation</term>
<term>Severe lupus nephritis</term>
<term>Severe nephritis</term>
<term>Spontaneous abortion</term>
<term>Subacute cutaneous lupus erythematosus</term>
<term>Syndrome</term>
<term>Systemic</term>
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<front><div type="abstract" xml:lang="en">It has been estimated that about 3 in 10 000 people in Britain's cities have systemic lupus erythematosus (SLE)1 and the true figure may be higher.2 Forty years ago, approximately 50% of patients with SLE died within 4 years of diagnosis.3 Prospects have improved with refinements in therapy and the recognition of mild forms of the disease.</div>
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