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抗磷脂综合征患者出现复发性播散性血管内凝血和暴发性肝内血栓形成。

Recurrent disseminated intravascular coagulation and fulminant intra hepatic thrombosis in a patient with the anti-phospholipid syndrome.

作者信息

Stinson J, Tomkin G, McDonald G, Jackson F, Harrison M, Murray A, Feighery C, Jackson J

机构信息

Adelaide Hospital, Dublin, Ireland.

出版信息

Am J Hematol. 1990 Dec;35(4):281-2. doi: 10.1002/ajh.2830350413.

Abstract

We describe a patient with the lupus anti-coagulant who had recurrent episodes, over a 2 year period, of a severe and disseminated intravascular coagulopathy. This patient also had positive serological assays for syphilis and anti-cardiolipin antibodies. Associated with the coagulopathy were co-expressed episodes of liver disease, ultimately terminating in fulminant liver failure. At autopsy the features were characteristic of the Budd-Chiari syndrome. This is the first report to document how consumptive coagulopathy may present as a dominant feature of the anti-phospholipid syndrome. It also clearly describes an immune mediated thrombotic mechanism as a cause of hepatic veno-occlusive disorders. Furthermore, this case highlights the varied clinical spectrum of the anti-phospholipid syndrome and suggests that a high index of suspicion is required to ensure its diagnosis.

摘要

我们描述了一名患有狼疮抗凝物的患者,在两年时间里反复出现严重的播散性血管内凝血病变。该患者梅毒血清学检测和抗心磷脂抗体检测均呈阳性。与凝血病相关的是同时出现的肝病发作,最终发展为暴发性肝衰竭。尸检时的特征符合布加综合征。这是第一份记录消耗性凝血病如何可能作为抗磷脂综合征的主要特征出现的报告。它还清楚地描述了一种免疫介导的血栓形成机制作为肝静脉闭塞性疾病的病因。此外,该病例突出了抗磷脂综合征多样的临床谱,并表明需要高度怀疑才能确保其诊断。

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