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原发性抗磷脂综合征是一种获得性高凝状态伴发多系统疾病,可原发或继发于多种疾病。血清学标志是狼疮抗凝物质和抗心磷脂抗体。皮肤表现常见且可能为首发症状,作者报告1例侵袭型原发性抗磷脂综合征的病例。
Primary antiphospholipid syndrome is an acquired hypercoagulable state associated with multiple system diseases, either primary or secondary to a variety of diseases. Serological markers are lupus anticoagulant substances and anti-cardiolipin antibodies. Skin manifestations are common and may be the first symptom, the authors report a case of invasive primary antiphospholipid syndrome.