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1.
Tunis Med ; 100(1): 60-65, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35822334

RESUMO

INTRODUCTION: Factor XI deficiency is a rare coagulation disorder with variable bleeding manifestations. AIM: To evaluate the correlation between the degree of factorXI deficiency and the clinical expression of the disease. METHODS: Retrospective study, spanning 10 years from January 1, 2010 to December 31, 2019, concerning patients followed at the Hemophilia Center at Aziza Othmana Hospital in Tunis. The data were collected from the medical records. The determination of PT, APTT, fibrinogen level and coagulation factors are performed by coagulometric technique on STA® compact / ACL TOP®. FactorXI deficiency was confirmed on two different samples. Statistical analysis of the clinical-biological correlation was performed using the chi-square test. The significance level was 0.05. RESULTS: Twenty patients were collected. The mean age of discovery was 25 years with a sex ratio (M/F) =0.33. The circumstances of discovery were incidental in 14 patients. A family history of bleeding was reported in 30% of cases. Eight patients underwent surgery, six of whom had a simple postoperative course. The APTT was prolonged and isolated in 75% of cases. The hemostasis test was normal in 5 cases. The average FactorXI level was 24%. The tendency to bleed did not seem to be correlated with FactorXI levels. CONCLUSION: Prospective multicenter studies including molecular study would be necessary to better elucidate this rare disorder.


Assuntos
Deficiência do Fator XI , Adulto , Deficiência do Fator XI/complicações , Deficiência do Fator XI/diagnóstico , Deficiência do Fator XI/epidemiologia , Hemorragia , Humanos , Prontuários Médicos , Estudos Prospectivos , Estudos Retrospectivos
4.
Ann Biol Clin (Paris) ; 78(2): 206-209, 2020 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-32319951

RESUMO

Factor V deficiency is a rare hemostatic disorder. It may present with a diverse spectrum of symptoms due to a variety of mechanisms including development of autoantibodies associated with a number of conditions. We report a first case of factor V deficiency in Tunisian hemodialysis patient due to an autoantibody most likely secondary to antibiotic exposure responsible for an arteriovenous shunt thrombosis rather than bleeding. We discuss here the clinical and biological features of acquired factor V inhibitor and provide a short review of the current literature.


Assuntos
Derivação Arteriovenosa Cirúrgica/efeitos adversos , Autoanticorpos/sangue , Transtornos da Coagulação Sanguínea/etiologia , Fator V/imunologia , Diálise Renal , Trombose/etiologia , Idoso , Transtornos da Coagulação Sanguínea/sangue , Transtornos da Coagulação Sanguínea/diagnóstico , Fator V/antagonistas & inibidores , Humanos , Masculino , Complicações Pós-Operatórias/sangue , Complicações Pós-Operatórias/diagnóstico , Insuficiência Renal Crônica/sangue , Insuficiência Renal Crônica/complicações , Insuficiência Renal Crônica/terapia , Trombose/sangue , Trombose/diagnóstico , Tunísia
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