Evans Syndrome
نویسندگان
چکیده
منابع مشابه
Management of Evans syndrome.
Evans syndrome is an uncommon condition defined by the combination (either simultaneously or sequentially) of immune thrombocytopenia (ITP) and autoimmune haemolytic anaemia (AIHA) with a positive direct antiglobulin test (DAT) in the absence of known underlying aetiology. This condition generally runs a chronic course and is characterised by frequent exacerbations and remissions. First-line th...
متن کاملEvans' syndrome associated with dermatomyositis.
Autoimmune haematological complications in dermatomyositis are very uncommon. This case report describes autoimmune haemolytic anaemia and thrombocytopenia in a patient with dermatomyositis and pulmonary fibrosis.
متن کاملMegadose methylprednisolone for Evans syndrome.
I was pleased to read Berber et al’s 50 year-old patient with Evans syndrome which was published as a Letter to The Editor in the recent issue of the Journal of Turgut Ozal Medical Center (2013;20(3):289-290). But, it was surprised to me that mega dose methyl prednisolone (MDMP) treatment was not brought to attention which had been successfully used for these patients first time from our countr...
متن کاملVitiligo Universalis Associated with Evans Syndrome and Antiphospholipid Syndrome
The pathogenesis of vitiligo has been proposed as a destruction of melanocytes by autoimmune processes. Evans syndrome is the combination of autoimmune hemolytic anemia and immune-mediated thrombocytopenia. The antiphospholipid syndrome is characterized by arterial/venous thrombosis, recurrent pregnancy loss, or thrombocytopenia in the presence of antiphospholipid antibodies. We present a case ...
متن کاملEdematous Dermatomyositis with Probable Evans Syndrome.
Inflammatory diseases of the muscles and skin are rare and orphan conditions. Dermatomyositis is an idiopathic inflammatory disorder associated with typical muscle and/or skin manifestations. Presentation with edema, ie, edematous dermatomyositis, is an infrequent variant. We report a new case of edematous dermatomyositis and review the literature. A 52-year-old woman with no clinical history o...
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ژورنال
عنوان ژورنال: Journal of Medicine
سال: 1970
ISSN: 2075-5384,1997-9797
DOI: 10.3329/jom.v11i1.4280