003 A case of wong-type dermatomyositis with Anti-TIF1-γ antibody
نویسندگان
چکیده
منابع مشابه
Concise report Clinical features of anti-TIF1-a antibody-positive dermatomyositis patients are closely associated with coexistent dermatomyositis-specific autoantibodies and anti-TIF1-c or anti-Mi-2 autoantibodies
Objective. Myositis-specific autoantibodies (MSAs), which characterize certain forms of inflammatory myopathy, are useful in the diagnosis and prediction of prognosis in DM/PM. Anti-transcriptional intermediary factor 1-a (TIF1-a) antibodies were recently reported to be associated with cancer-associated DM in conjunction with anti-TIF1-g antibodies. This study aimed to identify a subset of DM p...
متن کاملClinical characteristics of patients with anti-TIF1-γ antibodies
OBJECTIVES Inflammatory myopathies are a group of idiopathic, heterogeneous systemic diseases affecting predominantly skeletal muscles, though they can also involve the skin and internal organs. The association between cancer and idiopathic inflammatory myopathies, particularly dermatomyositis, which is termed cancer-associated myositis (CAM), has been reported in the medical literature. A newl...
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15 صفحه اولAnti-Gliadin antibody in Psoriasis: A case-control study
Background and objective: Psoriasis is chronic inflammatory skin disorder with a wide variety of clinical presentations. Presence of anti-gliadin antibody (AGA) has been reported in 16% of psoriatic patients. This study was designed to determine the frequency of the presence of AGA in psoriatic patients. Materials and Methods: After recording the demographic data and the severity of disease acc...
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A 9-year old boy had severe muscle weakness and typical skin rash and EMG with diagnosis of dermatomyositis associated with erythrodermia with islands of normal skin and palmoplantar hyperkeratosis, which was reported. As PRP in skin biopsy. Association dermatomyositis with PRP is very rare.
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ژورنال
عنوان ژورنال: Journal of Investigative Dermatology
سال: 2019
ISSN: 0022-202X
DOI: 10.1016/j.jid.2019.03.079