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1.
Union Med Can ; 122(2): 103-8, 1993.
Article in French | MEDLINE | ID: mdl-8493737

ABSTRACT

The prevalence of antineutrophil cytoplasmic antibodies (ANCAs) was verified in 338 patients with various rheumatic diseases using the internationally standardized indirect immunofluorescence method. The method was improved by using ethidium bromide as a nuclear counterstain. We observed three patterns of fluorescence: the classical diffuse cytoplasmic granular staining (C); the perinuclear one (P) and a yet undescribed atypical cytoplasmic distribution (A). We thus found ANCAs in 14/15 (93%) patients with active Wegener's granulomatosis: 13 were C-ANCAs, 1 was P-ANCA. We also found ANCAs in 6/25 (22%) patients with other systemis vasculitides (essentially those with small vessel vasculitis): they were C-ANCAs (3 cases) or P-ANCAs (3 cases). Finally, ANCAs were detected in 10/185 patients with various autoimmune diseases (5 with rheumatoid arthritis and 5 with systemic lupus erythematosus): they were C-ANCAs (1 case), P-ANCAs (4 cases) or A-ANCAs (5 cases). No ANCAs were found in 100 control patients with miscellaneous diseases. The isotype distribution of ANCAs is essentially limited to IgG classes and the serum titre usually reflects disease activity. The technical improvement facilitates the distinction of ANCAs from other antinuclear and anticytoplasmic autoantibodies found in connective tissue diseases. Our data emphasize the clinical importance of ANCA detection and justify our efforts to develop more specific and quantitative assays.


Subject(s)
Autoantibodies/blood , Immunoglobulin G/blood , Rheumatic Diseases/blood , Antibodies, Antineutrophil Cytoplasmic , Autoantibodies/classification , Evaluation Studies as Topic , Fluorescent Antibody Technique/standards , Humans , Immunoglobulin G/classification , Prevalence , Rheumatic Diseases/classification , Rheumatic Diseases/epidemiology , Sensitivity and Specificity
2.
J Rheumatol ; 18(9): 1359-63, 1991 Sep.
Article in English | MEDLINE | ID: mdl-1836814

ABSTRACT

99mTc-pyrophosphate musculoskeletal imaging and 99mTc-red blood cell gated blood pool imaging were performed on 10 patients with documented polymyositis/dermatomyositis. Abnormal 99mTc-pyrophosphate uptake by peripheral muscles was found in 8 patients (6 mild, 2 marked). Cardiac uptake occurred in 5 patients and was 3+ in 2 with cardiovascular symptoms. These 2 patients also had abnormal EF on gated blood pool imaging. Patients without myocardial 99mTc-pyrophosphate uptake had normal EF. Patients with myocardial 99mTc-pyrophosphate uptake had abnormal wall motion, in proportion to the degree of uptake. Response to therapy and outcome were poorer in patients with marked scintigraphic changes. These findings suggest that the magnitude of 99mTc-pyrophosphate myocardial uptake may have prognostic implications in these patients.


Subject(s)
Cardiomyopathies/physiopathology , Dermatomyositis/physiopathology , Heart/physiopathology , Myositis/physiopathology , Papillary Muscles/physiopathology , Adolescent , Adult , Cardiomyopathies/diagnostic imaging , Cardiomyopathies/pathology , Child , Dermatomyositis/diagnosis , Dermatomyositis/pathology , Female , Heart/diagnostic imaging , Humans , Male , Middle Aged , Musculoskeletal System/diagnostic imaging , Musculoskeletal System/metabolism , Myositis/diagnosis , Myositis/pathology , Papillary Muscles/diagnostic imaging , Papillary Muscles/pathology , Radionuclide Imaging , Technetium Tc 99m Pyrophosphate
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