介绍(产科)
医学
皮肤病科
系统性狼疮
全身性疾病
免疫学
病理
外科
疾病
免疫病理学
作者
Ali Al Bshabshe,Hamdan Al Shehri,Ali Assiri,Abdulmoneim Jamil
出处
期刊:European Journal of Molecular and Clinical Medicine
日期:2018-01-01
卷期号:5 (1): 37-40
被引量:1
摘要
Evans syndrome is a rare autoimmune disorder with an unknown etiology. In this paper, we report the case of a 32-year-old Saudi woman living with Evans syndrome for more than 8 years (post-splenectomy) who was also diagnosed with systemic lupus erythematosus (SLE). She was admitted to our Hospital with severe headache and confusion due to cerebral venous thrombosis. The major hematologic manifestations of SLE were pancytopenia and the antiphospholipid syndrome, which are indicators of disease activity when all other possible causes are excluded. The patient was treated with anticoagulation and immunosuppressive therapy and subsequently showed significant improvements in thrombosis, thrombocytopenia, and anemia. This case report provides an overview of the association between Evan syndrome and SLE.
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