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Acquired haemophilia: Epidemiology, clinical presentation, diagnosis and treatment
被引:23
|作者:
Eva Mingot-Castellano, Maria
[1
]
Nunez, Ramiro
[2
,3
]
Javier Rodriguez-Martorell, Francisco
[2
,3
]
机构:
[1] Hosp Reg Univ Malaga, Unidad Gest Clin Interctr Hematol, Malaga, Spain
[2] Hosp Univ Virgen Macarena, Unidad Gest Clin Interctr Hematol, Seville, Spain
[3] Hosp Univ Virgen Rocio, IBIS, Seville, Spain
来源:
MEDICINA CLINICA
|
2017年
/
148卷
/
07期
关键词:
Acquired haemophilia;
Factor VIII;
Factor VIII Inhibitor;
Anti-Factor VIII autoantibodies;
Antihaemorragic treatment;
Eradication of factor VIII Inhibitor;
RECOMBINANT FACTOR VIIA;
ACTIVATED FACTOR-VII;
INHIBITOR DEVELOPMENT;
BETHESDA ASSAY;
MANAGEMENT;
RITUXIMAB;
ANTIBODIES;
POLYMORPHISMS;
SURVEILLANCE;
THERAPY;
D O I:
10.1016/j.medcli.2016.11.030
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
The development of circulating autoantibodies able to inhibit some coagulation proteins induces severe or even life-threatening bleeding. This disorder is called acquired haemophilia. This is a rare disease, although its impact may be underestimated because of the lack of records, the lack of knowledge by many specialists, the complexity of the laboratory diagnosis and, finally, because of the fulminant clinical presentation that often precludes diagnosis. Several studies established that mortality ranges between 9 and 33%. Not only haematologists but all physicians should be trained to follow the right steps to diagnose these patients as soon as possible in order to reduce such mortality rates. This review approaches the basic concepts dealing with the diagnosis and management of these patients and intends to assist physicians in identifying patients under suspicion of acquired haemophilia to correctly manage them and refer them to the appropriate Haemostasis Unit. (C) 2016 Elsevier Espana, S.L.U. All rights reserved.
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页码:314 / 322
页数:9
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