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本文引用的文献

1
Resolution of Hypoprothrombinemia-Lupus Anticoagulant Syndrome (HLAS) after multidrug therapy with rituximab: a case report and review of the literature.利妥昔单抗多药治疗后低凝血酶原血症-狼疮抗凝物综合征(HLAS)的缓解:病例报告及文献复习。
Haemophilia. 2013 Mar;19(2):e62-5. doi: 10.1111/hae.12027. Epub 2012 Sep 19.
2
Lupus anticoagulant-hypoprothrombinemia syndrome: report of 8 cases and review of the literature.狼疮抗凝物-低凝血酶原血症综合征:8例报告及文献复习
Medicine (Baltimore). 2012 Sep;91(5):251-260. doi: 10.1097/MD.0b013e31826b971f.
3
Lupus anticoagulants in two children--bleeding due to nonphospholipid-dependent antiprothrombin antibodies.两例儿童狼疮抗凝物:非磷脂依赖性抗凝血酶原抗体导致的出血。
Eur J Pediatr. 2012 Sep;171(9):1383-7. doi: 10.1007/s00431-012-1737-1. Epub 2012 Apr 19.
4
Lupus Anticoagulant-Hypoprothrombinemia syndrome (HLAS): report of one case in a familial infectious context.
Thromb Res. 2010 Aug;126(2):e139-40. doi: 10.1016/j.thromres.2009.11.025. Epub 2009 Dec 16.

获得性抗凝血酶原抗体:一种不常见的出血原因。

Acquired antiprothrombin antibodies: an unusual cause of bleeding.

作者信息

Carvalho Cristiana, Viveiro Carolina, Maia Paulo, Rezende Teresa

机构信息

Department of Pediatria, Centro Hospitalar de Leiria-Pombal, Leiria, Portugal.

出版信息

BMJ Case Rep. 2013 Jan 7;2013:bcr2012007948. doi: 10.1136/bcr-2012-007948.

DOI:10.1136/bcr-2012-007948
PMID:23299692
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3603953/
Abstract

Acquired inhibitors of coagulation causing bleeding manifestations are rare in children. They emerge, normally in the context of autoimmune diseases or drug ingestion, but transient and self-limiting cases can occur after viral infection. We describe, an otherwise healthy, 7-year-old girl who had gingival bleeding after a tooth extraction. The prothrombin time (PT) and the activated partial thromboplastin time (APTT) were both prolonged with evidence of an immediate acting inhibitor (lupic anticoagulant). Further coagulation studies demonstrated prothrombin (FII) deficiency and prothrombin directed (FII) antibodies. The serological tests to detect an underlying autoimmune disease were all negative. The coagulation studies normalised alongside the disappearance of the antibody. This article presents lupus anticoagulant hypoprothrombinaemia syndrome (LAHS) as a rare case of acquired bleeding diathesis in childhood.

摘要

获得性凝血抑制物导致出血表现的情况在儿童中很少见。它们通常在自身免疫性疾病或药物摄入的背景下出现,但病毒感染后也可能发生短暂和自限性的病例。我们描述了一名原本健康的7岁女孩,她在拔牙后出现牙龈出血。凝血酶原时间(PT)和活化部分凝血活酶时间(APTT)均延长,有即时作用抑制剂(狼疮抗凝物)的证据。进一步的凝血研究显示凝血酶原(FII)缺乏和凝血酶原定向(FII)抗体。检测潜在自身免疫性疾病的血清学检查均为阴性。随着抗体的消失,凝血研究恢复正常。本文介绍了狼疮抗凝物低凝血酶原血症综合征(LAHS),这是儿童期获得性出血素质的罕见病例。