The clinical significance of the lack of arterial or venous thrombosis in patients with congenital prothrombin or FX deficiency

Journal of Thrombosis and Thrombolysis

Volumn 29, Issue 3, 2010, Pages 299-302

  Girolami, Antonio ^a   Candeo, Nicole ^a   Vettore, Silvia ^a   Lombardi, Anna Maria ^a   Girolami, Bruno ^a  

^a UNIVERSITY OF PADOVA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

PROTHROMBIN COMPLEX;

AFIBRINOGENEMIA; ARTERY THROMBOSIS; ARTICLE; BLOOD CLOTTING FACTOR 10 DEFICIENCY; BLOOD CLOTTING FACTOR 11 DEFICIENCY; BLOOD CLOTTING FACTOR 5 DEFICIENCY; BLOOD CLOTTING FACTOR 7 DEFICIENCY; CLINICAL ARTICLE; DEEP VEIN THROMBOSIS; DISEASE ASSOCIATION; DISSEMINATED INTRAVASCULAR CLOTTING; DRUG MEGADOSE; FEMALE; HEMOPHILIA A; HUMAN; LUNG EMBOLISM; MALE; PRIORITY JOURNAL; PROTHROMBIN DEFICIENCY; VEIN THROMBOSIS; ARTERIOSCLEROSIS; BLOOD; BLOOD COAGULATION DISORDERS, INHERITED; FACTOR X DEFICIENCY; GENETICS; HYPOPROTHROMBINEMIAS; VENOUS THROMBOSIS;

ARTERIOSCLEROSIS; BLOOD COAGULATION DISORDERS, INHERITED; FACTOR X DEFICIENCY; HUMANS; HYPOPROTHROMBINEMIAS; VENOUS THROMBOSIS;

EID: 77957938334     PISSN: 09295305     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11239-009-0342-2     Document Type: Article

References (32)

1. Goodnough LT, Saito H, Ratnoff OD (1983) Thrombosis or myocardial infarction in congenital clotting factor abnormalities and chronic thrombocytopenias: a report of 21 patients and a review of 50 previously reported cases. Medicine (Baltimore) 62:248-255. doi:10.1097/00005792-198307000- 00004
2. Girolami A, Randi ML, Ruzzon E, Zanon E, Girolami B (2005) Myocardial infarction, other arterial thrombosis and invasive coronary procedures, in hemophilia B: a critical evaluation of reported cases. J Thromb Thrombolysis 20:43-46. doi:10.1007/s11239-005-2227-3 (Pubitemid 41300621)
3. Girolami A, Tezza F, Scapin M, Vettore S, Casonato A (2006) Arterial and venous thrombosis in patients with von Willebrand's disease: a critical review of the literature. J Thromb Thrombolysis 21:175-178. doi:10.1007/s11239-006- 5732-0
4. Girolami A, Scandellari R, Zanon E, Sartori R, Girolami B (2006) Non-catheter associated venous thrombosis in hemophilia A and B. A critical review of all reported cases. J Thromb Thrombolysis 21:279-284. doi:10.1007/s11239-006-6556-7 (Pubitemid 43676787)
5. Girolami A, Ruzzon E, Fabris F, Varvarikis C, Sartori R, Girolami B (2006) Myocardial infarction and other arterial occlusions in hemophilia a patients. A cardiological evaluation of all 42 cases reported in the literature. Acta Haematol 116:120-125. doi: 10.1159/000093642 (Pubitemid 44252768)
6. Caen J, Faur Y, Inceman S, Chassigneux J, Seligmann M, Anagnostopoulos T, Bernard J (1964) Ischemie bilaterale necrotic chez un cas de hypofibrinogenemie congenitale grave. Nouv Rev Fr Hematol 72:321-324
7. Marchal G, Duhamel G, Samama M, Flandrin G (1964) Thrombose massive des vaisseaux de une extremitè chez un cas de hypofibrinogenemie congenitale. Hemostase 4:81-89
8. De Mattia D, Regina G, Giordano P, Del Vecchio GC, Altomare M, Schettini F (1993) Association of congenital afibrinogenemia and K-dependent protein C deficiency-a case report. Angiology 44:745-749. doi:10.1177/000331979304400913
9. Oruc N, Tokat Y, Killi R, Tombuloglu M, Ilter T (2006) Budd-Chiari syndrome in an afibrinogenemic patient: a paradoxical complication. Dig Dis Sci 51:378-380. doi:10.1007/s10620-006-3141-z
10. Roqué H, Stephenson C, Lee MJ, Funai EF, Popiolek D, Kim E, Hart D (2004) Pregnancy-related thrombosis in a woman with congenital afibrinogenemia: a report of two successful pregnancies. Am J Hematol 76:267-270. doi:10.1002/ajh.20110 (Pubitemid 38828848)
11. Hanano M, Takahashi H, Itoh M, Shibata A (1992) Coexistence of congenital afibrinogenemia and protein C deficiency in a patient. Am J Hematol 41:57-60. doi:10.1002/ajh.2830410111
12. Brenner B, Wiis J (2007) Experience with recombinant-activated factor VII in 30 patients with congenital factor VII deficiency. Hematology 12:55-62. doi:10.1080/10245330601111573 (Pubitemid 46394871)
13. Simsek I, de Mazancourt P, Horellou MH, Erdem H, Pay S, Dinc A, Samama MM (2008) Afibrinogenemia resulting from homozygous nonsense mutation in A alpha chain gene associated with multiple thrombotic episodes. Blood Coagul Fibrinolysis 19:247-253. doi:10.1097/MBC.0b013e3282f564fd (Pubitemid 351498732)
14. Linenberger ML, Kindelan J, Bennett RL, Reiner AP, Côté HC (2000) Fibrinogen bellingham: a gamma-chain R275C substitution and a beta-promoter polymorphism in a thrombotic member of an asymptomatic family. Am J Hematol 64:242-250. doi: 10.1002/1096-8652 (200008) 64:4<242::AID- AJH2>3.0. CO;2-O
15. Girolami A, Ruzzon E, Tezza F, Scandellari R, Vettore S, Girolami B (2006) Arterial and venous thrombosis in rare congenital bleeding disorders: a critical review. Haemophilia 12:345-351. doi:10.1111/j.1365-2516.2006.01299.x
16. Akbalik M, Duru F, Fisgin T, Tasdemir HA, Incesu L, Albayrak D, Ozyurek E (2007) Cerebral thrombosis associated with heterozygous factor V Leiden mutation and high lipoprotein (a) level in a girl with factor XIII deficiency. Blood Coagul Fibrinolysis 18:371-374
17. Almeida A, Khair K, Hann I, Liesner R (2002) Unusual presentation of factor XIII deficiency. Haemophilia 8:703-705. doi: 10.1046/j.1365-2516.2002. 00658.x
18. García-Noblejas A, Osorio S, Durán AI, Córdoba R, Nistal S, Aguado B, Loscertales J, Gómez N (2005) Pulmonary embolism in a patient with severe congenital deficiency for factor V during treatment with fresh frozen plasma. Haemophilia 11:276-279. doi:10.1111/j.1365-2516.2005.01091. x (Pubitemid 40723804)
19. Marty S, Barro C, Chatelain B, Fimbel B, Tribout B, Reynaud J, Schved JF, Giansily-Blaizot M (2008) The paradoxical association between inherited factor VII deficiency and venous thrombosis. Haemophilia 14:564-570. doi:10.1111/j.1365-2516.2007. 01647.x
20. Arellano-Rodrigo E, Gironella M, Nicolau I, Vila M (2009) Clinical management of thrombosis in inherited factor VII deficiency: a description of two cases. Thromb Haemost 101:402-404
21. Lietz K, Kuehling SE, Parkhurst JB (2005) Hemorrhagic stroke in a child with protein S and factor VII deficiencies. Pediatr Neurol 32:208-210. doi:10.1016/j.pediatrneurol.2004.08.008 (Pubitemid 40269706)
22. Blatt PM, Lundblad RL, Kingdon HS, McLean G, Roberts HR (1974) Thrombogenic materials in prothrombin complex concentrates. Ann Intern Med 81:766-770
23. Kasper CK (1974) Postoperative thromboses in hemophilia B. N Engl J Med 289:160
24. Kessler CM (2005) New perspectives in hemophilia treatment. Am Soc Hematol Educ Program 1:429-435
25. Mukhopadhyay S, Saxena R, Kashyap R, Choudhry VP (2001) Danazol therapy in factor X deficiency. Haemophilia 7:504-506. doi:10.1046/j.1365-2516.2001. 00541.x (Pubitemid 32923257)
26. Lohrmann J, Becker RC (2008) New anticoagulants-the path from discovery to clinical practice. N Engl J Med 358:2827-2828. doi:10.1056/NEJMe0804291 (Pubitemid 351930860)
27. Alban S (2008) Pharmacological Strategies for inhibition of thrombin activity. Curr Pharm Des 14:1152-1175. doi:10.2174/138161208784246135 (Pubitemid 351997828)
28. Harenberg J, Wehling M (2008) Current and future prospects for anticoagulant therapy: inhibitors of factor Xa and factor IIa. Semin Thromb Hemost 34:39-57. doi:10.1055/s-2008-1066023 (Pubitemid 351640881)
29. Ratnoff O (1968) The demise of Mr Hageman. New Eng J Med 279:760-761
30. Harris MG, Exner T, Rickard KA, Kronenberg H (1985) Multiple cerebral thrombosis in Fletcher factor (prekallikrein) deficiency: a case report. Am J Hematol 19:387-393. doi:10.1002/ajh.2830 190409
31. Girolami A, Randi ML, Gavasso S, Lombardi AM, Spiezia F (2004) The occasional venous thromboses seen in patients with severe (homozygous) FXII deficiency are probably due to associated risk factors: a study of prevalence in 21 patients and review of the literature. J Thromb Thrombolysis 17:139-143. doi:10.1023/B:THRO.0000037670.42776.cd (Pubitemid 39157964)
32. Zeerleder S, Schloesser M, Redondo M, Wuillemin WA, Engel W, Furlan M, Lämmle B (1999) Reevaluation of the incidence of thromboembolic complications in congenital factor XII deficiency-a study on 73 subjects from 14 Swiss families. Thromb Haemost 82:1240-1246