灾难性抗磷脂综合征
医学
伊库利珠单抗
美罗华
抗磷脂综合征
血栓性血小板减少性紫癜
血栓形成
血栓性微血管病
环磷酰胺
疾病
免疫学
重症监护医学
内科学
血小板
抗体
化疗
补体系统
作者
Ricard Cervera,Ignasi Rodríguez‐Pintó,Gerard Espinosa
标识
DOI:10.1016/j.jaut.2018.05.007
摘要
The catastrophic antiphospholipid syndrome (CAPS) is a life-threating variant of the antiphospholipid syndrome characterized by the development of multiple thrombosis in a short period of time, usually ending up in the failure of function of several vital organs. Most CAPS episodes are related to a prothrombotic situation or precipitating factor such as infections, surgical procedures or malignant diseases. In patients with CAPS, the development of multiple thrombosis leads to an important cytokine release that worsens the already critical patient's situation. The disease usually involves the kidneys, the lungs and the heart, although any organ system can be affected. Although occasionally the disease affects large vessels, in the majority of cases it affects small vessels, leading to a disseminated microangiopathic syndrome resembling thrombotic thrombocytopenic purpura. Treatment is based on the administration of anticoagulants, corticosteroids, plasma exchange and/or intravenous immunoglobulins. Cyclophosphamide is recommended in those CAPS cases associated to systemic lupus erythematosus. Additionally, rituximab and eculizumab have been used in refractory cases. Mortality is still around 30% despite current treatment.
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