Mazzucchelli R, Barbadillo C, Youssef H, Bernaldo de Quiros L B, Mulero J, Andreu-Sanchez J L
Service of Rheumatology, Hospital Puerta de Hierro, Facultad de Medicina, Universidad Autonoma, Madrid, Spain.
Clin Exp Rheumatol. 1993 Nov-Dec;11(6):653-7.
During the last decade, antiphospholipid antibodies and their clinical manifestations have given rise to increasing interest and have been associated with a wide spectrum of clinic expression, including arterial and venous thrombosis, thrombocytopenia, recurrent fetal wastage, Coombs positive haemolysis, livedo reticularis and neurological abnormalities, commonly present as isolated recurrent events, and rarely characterized by fatal outcome. Recently, an acutely disseminated vasculopathy, the so-called "catastrophic antiphospholipid syndrome" (CAS) characterized by non-inflammatory vascular occlusion and frequency of fatal outcome, has been described. We present yet another case report of this new and poorly understood entity and review its antecedents, clinical manifestations, serological profile, treatment and outcome.
在过去十年间,抗磷脂抗体及其临床表现引发了越来越多的关注,并与一系列临床症状相关,包括动脉和静脉血栓形成、血小板减少、反复流产、库姆斯试验阳性溶血、网状青斑及神经异常,这些症状通常表现为孤立的复发事件,很少以致命结局为特征。最近,一种急性播散性血管病,即所谓的“灾难性抗磷脂综合征”(CAS)被描述出来,其特征为非炎性血管闭塞及高致死率。我们在此呈现这一鲜为人知的新病症的另一例病例报告,并对其病史、临床表现、血清学特征、治疗及预后进行综述。