Shortness of breath in systemic lupus erythematosus: a diagnostic and therapeutic dilemma
Investigations showed urea 14.6 mmol/l (normal 3-8) and creatinine 0.145 mmol/l (normal 0.045-0.090), normal creatine kinase and troponin-t, albumin 18 g/l (normal 31-44), haemoglobin 98 g/l (normal 115-160), platelets 130x109/l (normal 150-450x109/l), white cell count 3.6x109/l (normal 4.0-11.0x109...
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Published in | Annals of the rheumatic diseases Vol. 61; no. 7; pp. 588 - 590 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
London
BMJ Publishing Group Ltd and European League Against Rheumatism
01.07.2002
BMJ BMJ Publishing Group Ltd BMJ Publishing Group LTD |
Subjects | |
Online Access | Get full text |
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Summary: | Investigations showed urea 14.6 mmol/l (normal 3-8) and creatinine 0.145 mmol/l (normal 0.045-0.090), normal creatine kinase and troponin-t, albumin 18 g/l (normal 31-44), haemoglobin 98 g/l (normal 115-160), platelets 130x109/l (normal 150-450x109/l), white cell count 3.6x109/l (normal 4.0-11.0x109/l), C reactive protein 3 mg/l (normal 1-6), erythrocyte sedimentation rate 115 mm/1st h (normal 2-18), and 24 hour urine protein 4.2 g. She had a positive antinuclear antibody test (titre 1/2560) with extractable nuclear antigen specificity of anti-Ro/La/Sm/RNP autoantibodies, negative anticardiolipin antibodies, and dsDNA binding of 56 IU/ml (normal <7.0). DISCUSSION Cardiac involvement is a well recognised manifestation of SLE, and includes pericarditis reported in 50-74% of patients, endocardial involvement in 50-63%, premature atherosclerosis and primary myocardial involvement (myocarditis) in 8-81%, depending on series and diagnostic criteria. 1 Necropsy studies suggest that myocardial involvement is common, affecting up to 40% of cases, with areas of myocardial inflammation, necrosis, and fibrosis seen. 2 An endomyocardial biopsy is required for a confident diagnosis before death of myocarditis secondary to active SLE. |
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Bibliography: | PMID:12079896 href:annrheumdis-61-588.pdf istex:82F8596D9A8D14EF2FF9757CF1D13E146BEF0EDC ark:/67375/NVC-HX9P0278-Z local:0610588 Correspondence to: Dr F Goldblatt, Department of Immunology, Allergy and Arthritis, Flinders Medical Centre, South Road, Bedford Park, South Australia 5042 ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3 |
ISSN: | 0003-4967 1468-2060 |
DOI: | 10.1136/ard.61.7.588 |