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血栓形成事件发生时无抗磷脂抗体的抗磷脂综合征:短暂性“血清阴性”抗磷脂综合征?

Antiphospholipid syndrome without antiphospholipid antibodies at the time of the thrombotic event: transient 'seronegative' antiphospholipid syndrome?

作者信息

Miret C, Cervera R, Reverter J C, García-Carrasco M, Ramos M, Mollà M, Font J, Ingelmo M

机构信息

Systemic Autoimmune Diseases Unit, Hospital Clínic, Barcelona, Catalonia, Spain.

出版信息

Clin Exp Rheumatol. 1997 Sep-Oct;15(5):541-4.

PMID:9307863
Abstract

The antiphospholipid syndrome (APS) is characterized by the presence of venous and arterial thrombosis, recurrent fetal losses and thrombocytopenia, associated with the presence of antiphospholipid antibodies (aPL). This syndrome may be "primary" or may be associated with other diseases, mainly systemic lupus erythematosus (SLE). However, some patients present the clinical picture of this syndrome but without evidence of aPL in their serum. The term "seronegative" APS has been proposed to categorize these patients. Here with we present two patients with seronegativity for aPL at the time of a thrombotic event, but in whom these antibodies were detected 2 and 7 months later.

摘要

抗磷脂综合征(APS)的特征是存在静脉和动脉血栓形成、反复流产和血小板减少,并伴有抗磷脂抗体(aPL)。该综合征可能是“原发性”的,也可能与其他疾病相关,主要是系统性红斑狼疮(SLE)。然而,一些患者呈现出该综合征的临床表现,但血清中无aPL证据。“血清阴性”APS这一术语已被提出用于对这些患者进行分类。在此,我们报告两名在发生血栓事件时aPL血清学阴性,但在2个月和7个月后检测到这些抗体的患者。

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