Literature DB >> 19412729

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

Antonio Girolami1, Nicole Candeo, Silvia Vettore, Anna Maria Lombardi, Bruno Girolami.   

Abstract

Several reports have dealt with the occurrence of both arterial and venous thrombosis in patients with haemophilia A, haemophilia B, and von Willebrand disease. Similar thrombotic events have been occasionally reported also in rare congenital coagulation disorders, particularly in fibrinogen or FVII deficiencies. On the contrary no sure venous or arterial thrombotic event has ever been reported in congenital prothrombin or Factor X deficiency. The significance of this observation is discussed. This discrepancy cannot be explained on the basis of the rarity of the two conditions, since in similarly rare congenital bleeding disorders such as FV or FXIII deficiency a few patients with thrombosis have been described. It appears that only these two defects are able to allow a sure protection from thrombosis. These observations may indirectly support the rationale for the use of direct thrombin or Factor X inhibitors in the prophylaxis and/or therapy of thrombotic manifestations.

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Year:  2010        PMID: 19412729     DOI: 10.1007/s11239-009-0342-2

Source DB:  PubMed          Journal:  J Thromb Thrombolysis        ISSN: 0929-5305            Impact factor:   2.300


  31 in total

1.  [BILATERAL ISCHEMIC NECROSIS IN A CASE OF SEVERE CONGENITAL HYPOFIBRINOGENEMIA].

Authors:  J CAEN; Y FAUR; S INCEMAN; J CHASSIGNEUX; M SELIGMANN; T ANAGNOSTOPOULOS; J BERNARD
Journal:  Nouv Rev Fr Hematol       Date:  1964 Mar-Apr

Review 2.  Arterial and venous thrombosis in patients with von Willebrand's disease: a critical review of the literature.

Authors:  A Girolami; F Tezza; M Scapin; S Vettore; A Casonato
Journal:  J Thromb Thrombolysis       Date:  2006-04       Impact factor: 2.300

3.  Budd-Chiari syndrome in an afibrinogenemic patient: a paradoxical complication.

Authors:  Nevin Oruc; Yaman Tokat; Refik Killi; Murat Tombuloglu; Tankut Ilter
Journal:  Dig Dis Sci       Date:  2006-02       Impact factor: 3.199

4.  Clinical management of thrombosis in inherited factor VII deficiency: a description of two cases.

Authors:  Eduardo Arellano-Rodrigo; Mercedes Gironella; Inmaculada Nicolau; Miquel Vila
Journal:  Thromb Haemost       Date:  2009-02       Impact factor: 5.249

5.  New perspectives in hemophilia treatment.

Authors:  Craig M Kessler
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2005

Review 6.  Myocardial infarction and other arterial occlusions in hemophilia a patients. A cardiological evaluation of all 42 cases reported in the literature.

Authors:  A Girolami; E Ruzzon; F Fabris; C Varvarikis; R Sartori; B Girolami
Journal:  Acta Haematol       Date:  2006       Impact factor: 2.195

7.  Reevaluation of the incidence of thromboembolic complications in congenital factor XII deficiency--a study on 73 subjects from 14 Swiss families.

Authors:  S Zeerleder; M Schloesser; M Redondo; W A Wuillemin; W Engel; M Furlan; B Lämmle
Journal:  Thromb Haemost       Date:  1999-10       Impact factor: 5.249

8.  Danazol therapy in factor X deficiency.

Authors:  S Mukhopadhyay; R Saxena; R Kashyap; V P Choudhry
Journal:  Haemophilia       Date:  2001-09       Impact factor: 4.287

9.  Experience with recombinant-activated factor VII in 30 patients with congenital factor VII deficiency.

Authors:  Benjamin Brenner; Jørgen Wiis
Journal:  Hematology       Date:  2007-02       Impact factor: 2.269

Review 10.  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.

Authors:  A Girolami; M L Randi; S Gavasso; A M Lombardi; F Spiezia
Journal:  J Thromb Thrombolysis       Date:  2004-04       Impact factor: 2.300

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  7 in total

Review 1.  Thrombotic and Hemorrhagic Conditions Due to a Gain of Function of Coagulation Proteins: A Special Type of Clotting Disorders.

Authors:  Antonio Girolami; Elisabetta Cosi; Silvia Ferrari; Annamaria Lombardi; Fabrizio Fabris
Journal:  Clin Appl Thromb Hemost       Date:  2017-08-04       Impact factor: 2.389

2.  Myocardial infarction in two cousins heterozygous for ASN41HIS autosomal dominant variant of Bernard-Soulier syndrome.

Authors:  Antonio Girolami; Silvia Vettore; Fabrizio Vianello; Giulia Berti de Marinis; Fabrizio Fabris
Journal:  J Thromb Thrombolysis       Date:  2012-11       Impact factor: 2.300

3.  Comparative incidence of thrombosis in reported cases of deficiencies of factors of the contact phase of blood coagulation.

Authors:  A Girolami; N Candeo; G Berti De Marinis; E Bonamigo; B Girolami
Journal:  J Thromb Thrombolysis       Date:  2011-01       Impact factor: 2.300

Review 4.  Heparin, coumarin, protein C, antithrombin, fibrinolysis and other clotting related resistances: old and new concepts in blood coagulation.

Authors:  A Girolami; E Cosi; S Ferrari; B Girolami
Journal:  J Thromb Thrombolysis       Date:  2018-01       Impact factor: 2.300

Review 5.  New clotting disorders that cast new light on blood coagulation and may play a role in clinical practice.

Authors:  A Girolami; E Cosi; S Ferrari; A M Lombardi; B Girolami
Journal:  J Thromb Thrombolysis       Date:  2017-07       Impact factor: 2.300

Review 6.  Associated prothrombotic conditions are probably responsible for the occurrence of thrombosis in almost all patients with congenital FVII deficiency. Critical review of the literature.

Authors:  A Girolami; F Tezza; R Scandellari; S Vettore; B Girolami
Journal:  J Thromb Thrombolysis       Date:  2010-08       Impact factor: 2.300

7.  Prekallikrein deficiency presenting as recurrent cerebrovascular accident: case report and review of the literature.

Authors:  Esteban Uribe Bojanini; Arturo Loaiza-Bonilla; Agustin Pimentel
Journal:  Case Rep Hematol       Date:  2012-08-16
  7 in total

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