Associated prothrombotic conditions are probably responsible for the occurrence of thrombosis in almost all patients with congenital FVII deficiency. Critical review of the literature

Journal of Thrombosis and Thrombolysis

Volumn 30, Issue 2, 2010, Pages 172-178

  Girolami, A ^a   Tezza, F ^a   Scandellari, R ^a   Vettore, S ^a   Girolami, B ^b  

^a UNIVERSITY OF PADOVA   (Italy)

^b Padua City Hospital   (Italy)

Author keywords

Associated prothrombotic risks; Factor VII deficiency; Thrombosis

Indexed keywords

ACETYLSALICYLIC ACID; BLOOD CLOTTING FACTOR 7; COUMARIN; DIPYRIDAMOLE; HEPARIN; LOW MOLECULAR WEIGHT HEPARIN; PROTHROMBIN COMPLEX;

ADOLESCENT; ADULT; AGED; ANTICOAGULANT THERAPY; ARTICLE; BLOOD CLOTTING FACTOR 7 DEFICIENCY; CENTRAL RETINA VEIN OCCLUSION; CEREBRAL SINUS THROMBOSIS; CEREBROVASCULAR ACCIDENT; CHILD; CLINICAL ARTICLE; DEEP VEIN THROMBOSIS; DISEASE ASSOCIATION; DISEASE SEVERITY; DISSEMINATED INTRAVASCULAR CLOTTING; FEMALE; HEART INFARCTION; HUMAN; LERICHE SYNDROME; LUNG EMBOLISM; MALE; MEDICAL LITERATURE; PERIPHERAL VEIN; PRIORITY JOURNAL; RISK ASSESSMENT; RISK FACTOR; SCHOOL CHILD; SPLANCHNIC BLOOD FLOW; SUBSTITUTION THERAPY; THROMBOSIS; TREATMENT RESPONSE; BLOOD; COMPLICATION; EVIDENCE BASED MEDICINE; GENETIC PREDISPOSITION; GENETICS; MIDDLE AGED; VERY ELDERLY; YOUNG ADULT;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CHILD; EVIDENCE-BASED MEDICINE; FACTOR VII DEFICIENCY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; RISK ASSESSMENT; RISK FACTORS; THROMBOSIS; YOUNG ADULT;

EID: 77957936876     PISSN: 09295305     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11239-009-0435-y     Document Type: Article

References (35)

1. Girolami A, Ruzzon E, Fabris F et al (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
2. Girolami A, Scandellari R, Zanon E et al (2006) Non-catheter associated venous thrombosis in hemophilia A and B. A critical review of all reported cases. J Thromb Thrombolysis 2:279-284
3. Franchini M (2004) Thrombotic complications in patients with hereditary bleeding disorders. Thromb Haemost 92:298-304 (Pubitemid 39172310)
4. 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 (Baltim) 62:248-255
5. Girolami A, Tezza F, Scapin M et al (2006) Arterial and venous thrombosis in patients with von Willebrand's disease: a critical review of the literature. J Thromb Thrombolysis 21:175-178
6. Girolami A, Randi ML, Ruzzon E et al (2005) Myocardial infarction, other arterial thrombosis and invasive coronary procedures, in hemaophilia B: a critical evaluation of reported cases. J Thromb Thrombolysis 20:43-46
7. Girolami A, Ruzzon E, Tezza F et al (2006) Arterial and venous thrombosis in rare congenital bleeding disorders: a critical review. Haemophilia 12:345-351
8. Solanki DL, Corn M (1980) Thromboembolism in patient with hereditary deficiency of coagulation factors. South Med J 73:944-946
9. Hall CA, Rapaport SI, Ames SB, Degroot JA (1964) A clinical and family study of hereditary proconvertin (factor VII) deficiency. Am J Med 37:172-181
10. Heikinheimo R, Reinikainen M (1969) Congenital factor VII deficiency. Two cases in children of cousins. Thromb Diath Haemorrh 21:245-248
11. Godal HC, Madsen K, Meyer RN (1962) Thrombo-embolism in patients with total proconvertin (factor VII) deficency. A report on two cases. Acta Med Scand 171:325-327
12. Kang HS, Kim DG, Yoon BW (1998) Superior sagittal sinus thrombosis with homocystinuria and deficiency of antithrombin III and factor VII: case report. Acta Neurochir (Wien) 140:196-198
13. Lefrere JJ, Chaunu MP, Canard J et al (1985) Congenital factor VII deficiency and cerebrovascular stroke. Lancet 2:1006-1007
14. Lietz K, Kuehling SE, Parkhurst JB (2005) Hemorrhagic stroke in a child with protein S and factor VII deficiencies. Pediatr Neurol 32:208-210
15. Nakagawa K, Furusawa A, Momono S et al (1990) Gastrectomy for a patient with congenital factor VII deficiency: a case report. Nippon Geka Gakkai Zasshi 91:771-773
16. Mariani G, Herrmann FH, Schulman S et al (2003) International Factor VII Deficiency Study Group. Thrombosis in inherited factor VII deficiency. J Thromb Haemost 1:2153-2158
17. Marty S, Barro C, Chatelain B et al (2008) The paradoxical association between inherited factor VII deficiency and venous thrombosis. Haemophilia 14:564-570
18. Bernardi F, Castaman G, Pinotti M et al (1996) Mutation pattern in clinically asymptomatic coagulation factor VII deficiency. Hum Mutat 8:108-115
19. 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
20. Cooke WL (1968) Acute myocardial infarction with decreased factor VII. W Va Med J 64:248-249
21. Ben Dridi MF, Karoui S, Kastally R et al (1986) L'homocystinuria. Forme avec thrombose vasculaire et deficit en facteur VII (Homocystinuria. A type with vascular thrombosis and factor VII deficiency). Arch Fr Pediatr 43:41-44
22. Escoffre M, Zini JM, Schliamser L, Mazoyer E, Soria C, Tobelem G, Dupuy E (1995) Severe arterial thrombosis in a congenitally factor VII deficient patient. Br J Haematol 91:739-741
23. Gershwin ME, Gude JK (1973) Deep vein thrombosis and pulmonary embolism in congenital factor VII deficiency. N Engl J Med 288:141-142
24. Girolami A, Fabris F, Dal Bo Zanon R et al (1978) Factor VII Padua: a congenital coagulation disorder due to an abnormal factor VII with a peculiar activation pattern. J Lab Clin Med 91:387-395
25. Shifter T, Machtey I, Creter D (1984) Thromboembolism in congenital factor VII deficiency. Acta Haematol 71:60-62
26. Sabharwal A, Kuppusiwamy M, Foster D et al (1992) Factor VII deficiency (FVII Richmond mutant R304A) associated with thrombosis. Circulation 86:679 (abstract)
27. Schulman S, Johnsson H, Lindmarker P (1991) Thrombotic complications after substitution with a FVII concentrate. Thromb Haemost 66:619
28. Ragni MV, Lewis JH, Spero JA, Hasiba U (1981) Factor VII deficicency. Am J Hematol 10:79-88
29. Worth LL, Hoots WK (1998) Development of a subdural vein thrombosis following aggressive factor VII replacement for postnatal intracranial haemorrhage in a homozygous factor VII-deficient infant. Haemophilia 4:757-761
30. Girolami A, Cattarozzi G, Dal Bo Zanon R, Toffanin F (1979) Factor VII Padua 2: another factor VII abnormality with defective ox brain thromboplastin activation and a complex hereditary pattern. Blood 54:46-53
31. Triplett DA, Brandt JT, Batard MA et al (1985) Hereditary factor VII deficiency: heterogeneity defined by combined functional and immunochemical analysis. Blood 66:1284-1287
32. Doshi SN, Marmur JD (2002) Evolving role of tissue factor and its pathway inhibitor. Crit Care Med 30 (Suppl): S241-S250
33. Piccioli A, Lensing AW, Prins MH, SOMIT Investigators Group et al (2004) Extensive screening for occult malignant disease in idiopathic venous thromboembolism: a prospective randomized clinical trial. J Thromb Haemost 2:884-889
34. Ratnoff OD, Busse RJ, Sheen RP (1968) The demise of Mr. Hageman. N Engl J Med 279:260-261
35. Girolami A, Candeo N, Vettore S et al (2009) The clinical significance of the lack of arterial or venous thrombosis in patients with congenital prothrombin or FX deficiency. J Thromb Thrombolysis. doi:10.1007/s11239-009- 0342-2