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小儿原发性抗磷脂综合征合并凝血因子Ⅱ缺乏症患者的灾难性出血

Catastrophic haemorrhage in a case of paediatric primary antiphospholipid syndrome and factor II deficiency.

作者信息

Hudson N, Duffy C M, Rauch J, Paquin J D, Esdaile J M

机构信息

Division of Rheumatology, Montreal General Hospital, PQ, Canada.

出版信息

Lupus. 1997;6(1):68-71. doi: 10.1177/096120339700600110.

DOI:10.1177/096120339700600110
PMID:9116722
Abstract

The first case of primary antiphospholipid syndrome associated with recurrent life-threatening haemorrhages, due to the coexistence of acquired prothrombin deficiency, is described. Attention is drawn to the difficulty in diagnosing this situation, and therapeutic options are reviewed. Evidence is presented that implicates prothrombin as the protein cofactor for this lupus anticoagulant.

摘要

本文描述了首例因获得性凝血酶原缺乏共存而导致复发性危及生命出血的原发性抗磷脂综合征病例。文中提请注意诊断这种情况的困难,并回顾了治疗选择。有证据表明凝血酶原是这种狼疮抗凝物的蛋白辅因子。

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引用本文的文献

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Pediatric APS: State of the Art.儿科抗磷脂综合征:现状。
Curr Rheumatol Rep. 2020 Mar 3;22(3):9. doi: 10.1007/s11926-020-0887-9.
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Lupus anticoagulant-hypoprothrombinemia syndrome and immunoglobulin-A vasculitis: a report of Japanese sibling cases and review of the literature.狼疮抗凝物-低凝血酶原血症综合征和免疫球蛋白 A 血管炎:日本同胞病例报告及文献复习。
Rheumatol Int. 2019 Oct;39(10):1811-1819. doi: 10.1007/s00296-019-04404-7. Epub 2019 Aug 7.
3
Transient antiphospholipid antibodies associated with acute infections in children: a report of three cases and a review of the literature.
Eur J Pediatr. 2006 Jul;165(7):484-8. doi: 10.1007/s00431-006-0117-0. Epub 2006 Mar 22.