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1
Bernard-Soulier syndrome in pregnancy with retinal detachment: a rare phenomenon.妊娠合并伯纳德-苏利耶综合征伴视网膜脱离:罕见现象。
BMJ Case Rep. 2022 Aug 31;15(8):e250405. doi: 10.1136/bcr-2022-250405.
2
Use of recombinant factor VIIa in the management of severe bleeding episodes in patients with Bernard-Soulier syndrome.重组凝血因子VIIa在伯纳德-索利尔综合征患者严重出血发作管理中的应用。
Ann Hematol. 2005 Nov;84(12):816-22. doi: 10.1007/s00277-005-1080-y. Epub 2005 Nov 12.
3
Bernard Soulier syndrome in pregnancy: a systematic review.妊娠伯纳德-苏利耶综合征:系统评价。
Haemophilia. 2010 Jul 1;16(4):584-91. doi: 10.1111/j.1365-2516.2009.02137.x. Epub 2010 Jan 12.
4
Bernard-Soulier Syndrome from the Perspective of the Obstetrician: A Case Report with a Review of the Literature.伯纳德-苏利耶综合征的产科视角:病例报告并文献复习。
Z Geburtshilfe Neonatol. 2023 Jun;227(3):168-178. doi: 10.1055/a-2024-0819. Epub 2023 Mar 8.
5
Course of pregnancy and birth in a patient with Bernard-Soulier syndrome--a case report.一名患有伯纳德-索利尔综合征患者的妊娠及分娩过程——病例报告
J Perinat Med. 2005;33(3):264-6. doi: 10.1515/JPM.2005.050.
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The genetic defect in two well-studied cases of Bernard-Soulier syndrome: a point mutation in the fifth leucine-rich repeat of platelet glycoprotein Ib alpha.两例经过充分研究的伯纳德-索利尔综合征的基因缺陷:血小板糖蛋白 Ibα 富含亮氨酸的重复序列 5 中的一个点突变。
Blood. 1995 Nov 15;86(10):3805-14.
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Bernard-Soulier syndrome with severe bleeding: absent platelet glycoprotein Ib alpha due to a homozygous one-base deletion.伴有严重出血的伯纳德-索利尔综合征:由于纯合单碱基缺失导致血小板糖蛋白 Ibα 缺失。
Thromb Haemost. 1996 Nov;76(5):670-4.
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[Obstetric and gynecological intervention in women with Bernard-Soulier syndrome: report of two cases].[Bernard-Soulier综合征女性的妇产科干预:两例报告]
Srp Arh Celok Lek. 2014 May-Jun;142(5-6):351-5. doi: 10.2298/sarh1406351m.
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Genetic abnormalities of Bernard-Soulier syndrome.伯纳德-索利尔综合征的基因异常。
Int J Hematol. 2002 Nov;76(4):319-27. doi: 10.1007/BF02982690.
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Coincidence of familial platelet glycoprotein Ib/IX deficiency (Bernard-Soulier syndrome), idiopathic autoantibody against platelet glycoprotein Ib/IX, familial appearance of antiphospholipid antibodies, and familial factor XII deficiency.
Ann Hematol. 1994 Feb;68(2):101-4. doi: 10.1007/BF01715142.

本文引用的文献

1
Management of Retinal Diseases in Pregnant Patients.妊娠患者视网膜疾病的管理
J Ophthalmic Vis Res. 2018 Jan-Mar;13(1):62-65. doi: 10.4103/jovr.jovr_195_17.
2
Management of Inherited Bleeding Disorders in Pregnancy: Green-top Guideline No. 71 (joint with UKHCDO).妊娠期遗传性出血性疾病的管理:第71号绿帽指南(与英国血液学临床医师协会联合发布)
BJOG. 2017 Jul;124(8):e193-e263. doi: 10.1111/1471-0528.14592. Epub 2017 Apr 27.
3
Glanzmann's thrombasthenia: pathogenesis, diagnosis, and current and emerging treatment options.血小板无力症:发病机制、诊断以及当前和新兴的治疗选择。
J Blood Med. 2015 Jul 8;6:219-27. doi: 10.2147/JBM.S71319. eCollection 2015.
4
Primigravida with Bernard-Soulier Syndrome: a case report.初产妇合并伯纳德-索利尔综合征:一例报告
BMC Res Notes. 2015 May 1;8:178. doi: 10.1186/s13104-015-1145-5.
5
Bilateral retinal detachment in a case of preeclampsia.子痫前期致双侧视网膜脱离。
Bosn J Basic Med Sci. 2011 May;11(2):129-31. doi: 10.17305/bjbms.2011.2598.
6
Bernard Soulier syndrome in pregnancy: a systematic review.妊娠伯纳德-苏利耶综合征:系统评价。
Haemophilia. 2010 Jul 1;16(4):584-91. doi: 10.1111/j.1365-2516.2009.02137.x. Epub 2010 Jan 12.
7
Fetomaternal platelet immunization associated with maternal Bernard-Soulier syndrome.与母亲伯纳德-索利尔综合征相关的母胎血小板免疫
Am J Perinatol. 2008 Apr;25(4):219-23. doi: 10.1055/s-2008-1064932.
8
Successful pregnancy outcome in Bernard-Soulier syndrome.Bernard-Soulier综合征患者成功的妊娠结局。
J Obstet Gynaecol Res. 2005 Feb;31(1):52-6. doi: 10.1111/j.1447-0756.2005.00240.x.
9
The PFA-100: a potential rapid screening tool for the assessment of platelet dysfunction.PFA-100:一种用于评估血小板功能障碍的潜在快速筛查工具。
Clin Lab Haematol. 2002 Aug;24(4):225-32. doi: 10.1046/j.1365-2257.2002.00451.x.
10
Inherited defects of platelet function.血小板功能的遗传性缺陷。
Rev Clin Exp Hematol. 2001 Dec;5(4):314-34; quiz following 431. doi: 10.1046/j.1468-0734.2001.00052.x.

妊娠合并伯纳德-苏利耶综合征伴视网膜脱离:罕见现象。

Bernard-Soulier syndrome in pregnancy with retinal detachment: a rare phenomenon.

机构信息

Centre for Reproductive Medicine and Surgery, St Bartholomew's Hospital, London, UK

Haemophilia and Thrombosis Centre, Belfast City Hospital Health and Social Services Trust, Belfast, UK.

出版信息

BMJ Case Rep. 2022 Aug 31;15(8):e250405. doi: 10.1136/bcr-2022-250405.

DOI:10.1136/bcr-2022-250405
PMID:36129357
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9438107/
Abstract

Bernard-Soulier syndrome (BSS) is a rare congenital bleeding disorder of the platelet, and it is mainly inherited as an autosomal recessive trait. It is caused by both qualitative and quantitative deficiency of the platelet membrane glycoprotein (GP) Ib-IX-V receptor complex, thereby causing abnormal platelets adhesion.We report a case of a primigravida in her 20s with history of BSS diagnosed in childhood due to family history. Her preconception period was challenging as she suffered from severe menorrhagia often requiring hospital admission, blood and platelet transfusions.At 35 weeks gestation, she developed temporal crowded retinal detachment of the left eye and had a successful left scleral buckling surgery under general anaesthesia (GA).She had a multidisciplinary team care with a successful elective GA caesarean section at 39+3 weeks gestation with peridelivery platelet transfusion and intravenous recombinant factor VIIa. Regional anaesthesia, intramuscular injections and anticoagulation were avoided.

摘要

伯纳德-苏利耶综合征(BSS)是一种罕见的血小板先天性出血性疾病,主要遗传方式为常染色体隐性遗传。其病因是血小板膜糖蛋白(GP)Ib-IX-V 受体复合物的质和量均有缺陷,导致血小板黏附异常。我们报告了一例 20 多岁的初产妇,她因家族史在儿童时期被诊断为 BSS。她的孕前阶段充满挑战,经常因严重月经过多而需要住院,接受输血和血小板输注。在 35 周妊娠时,她左眼发生短暂性视网膜脱离,在全身麻醉(GA)下成功进行了左眼巩膜扣带术。她接受了多学科团队的治疗,在 39+3 周妊娠时成功进行了选择性 GA 剖宫产术,分娩期间输注血小板和静脉内重组因子 VIIa。避免了区域麻醉、肌肉注射和抗凝治疗。