We report 3 patients with polymyositis and the anti-Jo-1 antibody who developed fatal adult respiratory distress syndrome (ARDS). Other than the presence of the anti-Jo-1 antibody, there were no other consistent clinical features at the onset of disease that were predictive of ARDS development.
A subluxing arthropathy associated with the anti-jo-1 antibody in polymyositis/dermatomyositis
✍ Scribed by Chester V. Oddis; Thomas A. Medsger Jr; Lawrence A. Cooperstein
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 505 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0004-3591
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✦ Synopsis
Of 180 patients with polymyositis/dermatomyositis (PM/DM) seen at the University of Pittsburgh and affiliated hospitals since 1975, 21 of 100 tested positive for the anti-Jo-1 antibody. Sixteen of the 21 patients were women and 18 were white. Fifteen had adult PM, 4 had myositis in overlap with scleroderma, and 2 had adult DM. Evidence of interstitial lung disease was found in 12 of 18 anti-Jo-1 positive patients (67%), but in only 15 of 79 anti-Jo-1 negative patients (19%) (P < 0.0002). The 21 anti-,To-1 positive patients were divided into 3 separate groups based on the observed articular findings. Four patients had a deforming, predominantly nonerosive arthropathy with subluxations of the distal interphalangeal joints, especially the thumbs. Eight patients had a nondeforming arthropathy primarily affecting the small joints of the hands, wrists, shoulders, and knees. Those with deformities had a longer duration From the Division of Rheumatology and Clinical Immunology and the Division of
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