Myocardial infarction and pulmonary embolism in a 45 year-old woman with the prothrombin 20210A mutation - a case report

被引:0
作者
Wozakowska-Kaplon, Beata [1 ,2 ]
Szydziak-Zwierzynska, Kinga [1 ]
机构
[1] Swietokrzyskie Ctr Kardiol, Oddzial Kardiol 1, PL-25736 Kielce, Poland
[2] Uniwersytet Humanistyczno Przyrodn Jana Kochanows, Wydzial Nauk Zdrowiu, Kielce, Poland
关键词
prothrombin muation G20210A; myocardial infarction; pulmonary embolism; FACTOR-V-LEIDEN; DEEP VENOUS THROMBOSIS; G20210A MUTATION; RISK-FACTORS; HETEROZYGOUS CARRIERS; GENETIC-VARIATION; VARIANT; PREVALENCE; THROMBOEMBOLISM; COAGULATION;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We present a case of a 45-year-old-female who developed myocardial infarction and 6 weeks following first hospitalisation - pulmonary embolism. The disease was probably triggered by hormone replacement therapy. Coronary angioplasty and anticoagulant therapy with unfractioned heparin and acenokumarol were used with success. The woman and her 17-year-old daughter were shown to be heterozygous for prothrombin mutation G20210A This case shows that trombophilia should be considered in young women with deep venous thrombosis, pulmonary embolism, venous thromboembolism or with myocardial infarction especially in women with high-risk factors.
引用
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页码:162 / 167
页数:6
相关论文
共 33 条
[1]  
Ardissino D, 1999, BLOOD, V94, P46
[2]  
Aznar J, 2000, HAEMATOLOGICA, V85, P1271
[3]   Genetic variation in coagulation and fibrinolytic proteins and their relation with acute myocardial infarction [J].
Boekholdt, SM ;
Bijsterveld, NR ;
Moons, AHM ;
Levi, M ;
Büller, HR ;
Peters, RJG .
CIRCULATION, 2001, 104 (25) :3063-3068
[4]   Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease [J].
Burzotta, F ;
Paciaroni, K ;
De Stefano, V ;
Chiusolo, P ;
Manzoli, A ;
Casorelli, I ;
Leone, AM ;
Rossi, E ;
Leone, G ;
Maseri, A ;
Andreotti, F .
EUROPEAN HEART JOURNAL, 2002, 23 (01) :26-30
[5]   G20210A prothrombin gene polymorphism and coronary ischaemic syndromes: a phenotype-specific meta-analysis of 12 034 subjects [J].
Burzotta, F ;
Paciaroni, K ;
De Stefano, V ;
Crea, F ;
Maseri, A ;
Leone, G ;
Andreotti, F .
HEART, 2004, 90 (01) :82-86
[6]   Prevalence of factor V Leiden and prothrombin G20210A mutations in unselected patients with venous thromboembolism [J].
de Moerloose, P ;
Reber, G ;
Perrier, A ;
Perneger, T ;
Bounameaux, H .
BRITISH JOURNAL OF HAEMATOLOGY, 2000, 110 (01) :125-129
[7]   The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation [J].
De Stefano, V ;
Martinelli, I ;
Mannucci, PM ;
Paciaroni, K ;
Chiusolo, P ;
Casorelli, I ;
Rossi, E ;
Leone, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (11) :801-806
[8]   The risk of recurrent venous thromboembolism among heterozygous carriers of the G20210A prothrombin gene mutation [J].
De Stefano, V ;
Martinelli, I ;
Mannucci, PM ;
Paciaroni, K ;
Rossi, E ;
Chiusolo, P ;
Casorelli, I ;
Leone, G .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 113 (03) :630-635
[9]   Prothrombin 20210GA and factor V Leiden mutations in patients less than 55 years old with myocardial infarction [J].
Dönmez, Y ;
Kanadasi, M ;
Tanriverdi, K ;
Demir, M ;
Demirtas, M ;
Çayli, M ;
Alhan, C ;
Baslamisli, F .
JAPANESE HEART JOURNAL, 2004, 45 (03) :505-512
[10]   The prothrombin G20210A polymorphism in patients with myocardial infarction [J].
Durante-Mangoni, E ;
Davies, GJ ;
Ahmed, N ;
Ruggiero, G ;
Michaelides, K .
BLOOD COAGULATION & FIBRINOLYSIS, 2002, 13 (07) :603-608