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子宫压迫法成功治疗Glanzmann血小板无力症所致急性灾难性青少年阴道出血:一例报告并文献复习

Successful Management of Acute Catastrophic Juvenile Vaginal Bleeding in Glanzmann's Thromboasthenia by Uterine Tamponade: A Case Report and Review of The Literature.

作者信息

Hossain Nazli, Shamsi Tahir S, Feroz Adeel

机构信息

Department of Obstetrics & Gynecology Unit 3, Dow University of Health Sciences, Baba-e-Urdu Road, Karachi 74200, Pakistan.

出版信息

Case Rep Hematol. 2012;2012:530908. doi: 10.1155/2012/530908. Epub 2012 Mar 20.

DOI:10.1155/2012/530908
PMID:22928124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3420404/
Abstract

Glanzmann's thromboasthenia (GT) is a rare platelet disorder, due to membrane defects involving glycoprotein GP IIb/IIIa complex. Symptoms appear in infancy with episodes of bruising, gingival bleeding, epistaxis, or at the time of menarche acute episode of uterine bleeding. Hormonal therapy and antifibrinolytic agents are first-line treatment. Platelet transfusion is given to control hemorrhage when medical treatment fails. However, repeated transfusions may result in development of platelet refractioness, due to development of antibodies against membrane glycoprotein. Activated recombinant FVII is licensed for use in acute control of bleeding in GT. Here we report a case of acute juvenile uterine bleeding at menarche, which responded successfully to uterine tamponade. To our knowledge, this is the first case report on use of balloon tamponade for control of acute catastrophic juvenile bleeding at menarche.

摘要

Glanzmann血小板无力症(GT)是一种罕见的血小板疾病,由涉及糖蛋白GP IIb/IIIa复合物的膜缺陷引起。症状在婴儿期出现,表现为瘀伤、牙龈出血、鼻出血,或在初潮时出现子宫急性出血。激素治疗和抗纤维蛋白溶解剂是一线治疗方法。当药物治疗无效时,给予血小板输注以控制出血。然而,由于针对膜糖蛋白的抗体产生,反复输血可能导致血小板输注无效。活化重组FVII已获许可用于GT出血的急性控制。在此,我们报告一例初潮时急性青少年子宫出血病例,该病例成功通过子宫压迫止血。据我们所知,这是首例关于使用球囊压迫控制初潮时急性灾难性青少年出血的病例报告。

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本文引用的文献

1
Management of abnormal uterine bleeding in adolescents.青少年异常子宫出血的管理
J Pediatr Adolesc Gynecol. 2010 Dec;23(6 Suppl):S22-30. doi: 10.1016/j.jpag.2010.08.007. Epub 2010 Sep 24.
2
Bleeding disorders in the tribe: result of consanguineous in breeding.部落中的出血性疾病:近亲繁殖的结果。
Orphanet J Rare Dis. 2010 Sep 7;5:23. doi: 10.1186/1750-1172-5-23.
3
Control of severe bleeding episode in case of Glanzmann's thrombasthenia refractory to platelet transfusion therapy by administering recombinant factor VIIa.通过给予重组凝血因子VIIa来控制对血小板输注治疗难治的Glanzmann血小板无力症患者的严重出血发作。
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Adolescent menorrhagia due to platelet function disorder.血小板功能障碍所致青春期月经过多
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Allogeneic stem cell transplantation for Glanzmann thrombasthenia.用于治疗Glanzmann血小板无力症的异基因干细胞移植。
Pediatr Blood Cancer. 2009 May;52(5):682-3. doi: 10.1002/pbc.21888.
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Congenital disorders associated with platelet dysfunctions.与血小板功能障碍相关的先天性疾病。
Thromb Haemost. 2008 Feb;99(2):253-63. doi: 10.1160/TH07-09-0568.
7
The prevalence of disorders of haemostasis in adolescents with menorrhagia referred to a haemophilia treatment centre.因月经过多而转诊至血友病治疗中心的青少年中止血障碍的患病率。
Haemophilia. 2007 Sep;13(5):627-32. doi: 10.1111/j.1365-2516.2007.01496.x.
8
Uterine artery embolization for control of life-threatening hemorrhage at menarche: brief report.子宫动脉栓塞术用于控制初潮时危及生命的出血:简要报告。
J Vasc Interv Radiol. 2007 Jan;18(1 Pt 1):127-31. doi: 10.1016/j.jvir.2006.10.015.
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Menorrhagia due to abnormalities of the platelet function: evaluation of two young patients.血小板功能异常所致月经过多:两名年轻患者的评估
Pediatr Int. 2007 Feb;49(1):106-8. doi: 10.1111/j.1442-200X.2007.02304.x.
10
Glanzmann thrombasthenia.血小板无力症
Orphanet J Rare Dis. 2006 Apr 6;1:10. doi: 10.1186/1750-1172-1-10.