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Female case with misdiagnosis of hemophilia A who underwent total knee arthroplasty: A case report.1例误诊为甲型血友病的女性患者行全膝关节置换术：病例报告
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2
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Evaluation of von Willebrand factor phenotypes and genotypes in Hemophilia A patients with and without identified F8 mutations.对有无已鉴定出F8突变的A型血友病患者血管性血友病因子表型和基因型的评估。
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Postoperative bleeding adversely affects total knee arthroplasty outcomes in hemophilia.术后出血对血友病患者全膝关节置换术的预后产生不利影响。
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本文引用的文献

1
Successful Surgical Removal of A Massive Iliopsoas Pseudotumor in a Boy With Mild Hemophilia A.成功手术切除一名患有轻度甲型血友病男孩的巨大髂腰肌假肿瘤。
Klin Padiatr. 2018 Oct;230(6):333-335. doi: 10.1055/a-0586-4514. Epub 2018 Mar 27.
2
Clinical and laboratory approaches to hemophilia a.甲型血友病的临床与实验室研究方法
Iran J Med Sci. 2015 May;40(3):194-205.
3
Investigation of inflicted injury in a young girl reveals mild haemophilia A and Turner's syndrome.对一名年轻女孩遭受的伤害进行调查，结果显示她患有轻度血友病 A 和特纳综合征。
Int J Lab Hematol. 2012 Feb;34(1):98-101. doi: 10.1111/j.1751-553X.2011.01347.x. Epub 2011 Jun 27.
4
Phenotypic heterogeneity in severe hemophilia.重度血友病的表型异质性。
J Thromb Haemost. 2007 Jul;5 Suppl 1:151-6. doi: 10.1111/j.1538-7836.2007.02503.x.
5
A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD).1型血管性血友病出血症状的定量分析：一项欧洲多中心研究（MCMDM-1 VWD）的结果
J Thromb Haemost. 2006 Apr;4(4):766-73. doi: 10.1111/j.1538-7836.2006.01847.x.
6
Haemophilias A and B.血友病A和B。
Lancet. 2003 May 24;361(9371):1801-9. doi: 10.1016/S0140-6736(03)13405-8.
7
Impact, diagnosis and treatment of von Willebrand disease.血管性血友病的影响、诊断及治疗
Thromb Haemost. 2000 Aug;84(2):160-74.
8
Biochemistry and genetics of von Willebrand factor.血管性血友病因子的生物化学与遗传学
Annu Rev Biochem. 1998;67:395-424. doi: 10.1146/annurev.biochem.67.1.395.
9
A revised classification of von Willebrand disease. For the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.血管性血友病的修订分类。国际血栓与止血协会科学和标准化委员会血管性血友病因子小组委员会制定。
Thromb Haemost. 1994 Apr;71(4):520-5.

1例误诊为甲型血友病的女性患者行全膝关节置换术：病例报告

Female case with misdiagnosis of hemophilia A who underwent total knee arthroplasty: A case report.

作者信息

Bari Alireza, Mansouritorghabeh Hassan

机构信息

Department of Hematology Ghaem Hospital Mashhad University of Medical Sciences Mashhad Iran.

Central Diagnostic Laboratories Ghaem Hospital Mashhad University of Medical Sciences Mashhad Iran.

出版信息

Clin Case Rep. 2022 Mar 14;10(3):e05558. doi: 10.1002/ccr3.5558. eCollection 2022 Mar.

DOI:10.1002/ccr3.5558
PMID:35310320
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8919699/
Abstract

A female was diagnosed with hemophilia A. She had undergone bilateral total knee arthroplasty. She had a history of numerous hemorrhages including hemarthrosis. After further investigations, the diagnosis of von Willebrand disease type 2N was confirmed. The differential diagnoses for hemophilia A include von Willebrand disease, rare bleeding disorders, and severe platelet disorders.

摘要

一名女性被诊断为甲型血友病。她接受了双侧全膝关节置换术。她有多次出血史，包括关节积血。经过进一步检查，确诊为2N型血管性血友病。甲型血友病的鉴别诊断包括血管性血友病、罕见的出血性疾病和严重的血小板疾病。