Calcinosis Universalis
نویسندگان
چکیده
منابع مشابه
Idiopathic calcinosis cutis universalis
Case A 12-years old girl with complaints of multiple lumps on her body since 1 years prior to admission. Two years prior to admission patient complained of movement limitation due to pain when doing leg lifting, squatting and standing up. One years prior to admission patient got bilateral symmetrical lumps on hip, corn size and getting bigger. Two months prior to admission the lumps got rupture...
متن کاملTreatment of calcinosis universalis with aluminium hydroxide.
This male child was born in February 1958. In early infancy he had an operation of the left kidney, but otherwise he was well until the age of 31 years when he developed a skin rash and muscle contractures. Dermatomyositis was diagnosed, and the result of a muscle biopsy was as follows. 'The muscle shows areas of oedema, a patchy but diffuse inflammatory cell infiltrate composed of lymphocytes,...
متن کاملTherapy of calcinosis universalis complicating adult dermatomyositis.
Although frequent in juvenile dermatomyositis, calcinosis is a rare finding in adult dermatomyositis. It has been associated with disease activity and delayed treatment. It is more common in later phases of the disease, in sites under chronic stress and trauma. Calcinosis has been associated with inflammation but information about its pathogeny continues to evolve as we learn more about the und...
متن کاملCalcinosis 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 کاملExtensive soft tissue calcification (calcinosis universalis) in systemic lupus erythematosus.
A 21-year-old woman with long-standing systemic lupus erythematosus developed extensive calcification of the soft tissues of the thoracic and abdominal walls and extremities early in her illness, and these calcifications gradually disappeared over the course of her disease. The extent of this calcinosis and apparent spontaneous regression are unusual events in systemic lupus erythematosus.
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ژورنال
عنوان ژورنال: Proceedings of the Royal Society of Medicine
سال: 1934
ISSN: 0035-9157
DOI: 10.1177/003591573402700601