Unusual sequelae of adult-onset dermatomyositis
نویسندگان
چکیده
منابع مشابه
Calcinosis universalis in adult-onset dermatomyositis.
To cite: Bernardino V, Rodrigues A, Panarra A, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2015211142 DESCRIPTION A 67-year-old woman of African origin with dermatomyositis, diagnosed 18 years before, and dystrophic calcification known for 5 years, presented at follow-up consultation with fever, increased muscle weakness (scapular and pelvic chains) and...
متن کاملSubcutaneous fat calcinosis in adult-onset dermatomyositis.
1 of 2 DESCRIPTION Calcinosis is a well-documented manifestation seen in up to 40% of patients with juvenile dermatomyositis. It is an uncommon feature in adult-onset dermatomyositis. 1 We present a rare occurrence of calcinosis with unusual distribution in a 51-year-old male. 18-months after diagnosis, our patient was seen in clinic following an episode of cellulitis. His muscle weakness and s...
متن کاملUnusual manifestations and unusual mimics of adult onset Still’s disease
[No Abstract Available].
متن کاملAn Unusual Presentation of Adult Onset Still's Disease.
Adult onset still's disease usually presents with high grade intermittent fever, polyarthritis, salmon pink evanescent rash and hepatosplenomegaly. Pulmonary involvement in the form of pneumonitis, as a presenting feature is very rare. We report a case of a young lady who presented with fever, cough and respiratory distress. Chest X-ray revealed patchy infiltration in left upper lung zone. She ...
متن کاملSpontaneous pneumomediastinum in adult dermatomyositis.
Spontaneous pneumomediastinum has not been reported in adult polymyositis or dermatomyositis, either in conjunction with spontaneous pneumothorax or in isolation. Spontaneous pneumothorax has been rarely reported as a complication of rheumatoid arthritis, systemic lupus erythematosus, scleroderma, and childhood dermatomyositis. It is associated with active, progressive pulmonary involvement and...
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ژورنال
عنوان ژورنال: Case Reports
سال: 2014
ISSN: 1757-790X
DOI: 10.1136/bcr-2014-204521