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Antiphospholipid Syndrome: A complex disease

机译:抗磷脂综合症:一种复杂的疾病

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In the last three decades, a variety of clinical manifestations involving almost all organs and tissues (cardiac, pulmonary, neurological, renal, cutaneous, haematologic, gastrointestinal, ocular, skeletal and endocrinologic), have been described associated with antiphospholipid antibodies (aPL) . Nevertheless, the exact mechanism underlying the pathogenesis of aPL-mediated damage has been poorly recognized. Inflammatory mechanisms beyond thrombosis have been proposed in some clinical presentations, suggesting a role for immunomodulation in therapeutic strategy
机译:在过去的三十年中,已经描述了涉及几乎所有器官和组织(心脏,肺,神经,肾,皮肤,血液,胃肠道,眼,骨骼和内分泌)的多种临床表现,与抗磷脂抗体(aPL)相关。然而,人们尚不清楚aPL介导的损伤的发病机理的确切机制。在一些临床研究中已经提出了血栓形成以外的炎症机制,提示免疫调节在治疗策略中的作用

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