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How do we encounter rare factor deficiencies in children? Single-centre results from Turkey.
Tugcu, Deniz; Salcioglu, Zafer; Akcay, Arzu; Sen, Hülya S; Aydogan, Gönül; Akici, Ferhan; Keskindemirci, Gonca; Ayaz, Nuray A; Baslar, Zafer.
Afiliação
  • Tugcu D; aDepartment of Pediatric Hematology and Oncology, Istanbul Kanuni Sultan Suleyman Education and Research Hospital bDepartment of Internal Medicine, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey.
Blood Coagul Fibrinolysis ; 26(2): 145-51, 2015 Mar.
Article em En | MEDLINE | ID: mdl-25390505
ABSTRACT

BACKGROUND:

Rare factor deficiencies (RFDs) are autosomal recessively inherited coagulation factor deficiencies encountered at a frequency of between one in 500, 000 and one in two million. MATERIALS AND

METHODS:

One hundred and ninety-two patients, diagnosed as having RFD, followed and treated in our clinic between 1990 and 2013 were retrospectively evaluated in this study.

RESULTS:

From the 192 patients, 142 had FVII, 15 had FX, 14 had FXI, 10 had fibrinogen, six had FV, two had FXIII, two had FV + FVIII and one had FII deficiency. One hundred and thirty of the cases were boys and 62 were girls. The age range was 2 weeks to 24 years and the ages at the admission were between 2 weeks and 16 years. The rate of consanguinity was 49.4%. Eighty-eight of our patients were asymptomatic (45.8%) and 104 were symptomatic (54.2%). Asymptomatic patients were diagnosed by family histories (39.8%), preoperative laboratory studies (54.6%) and operational bleeding (5.6%). Sixty-eight of our symptomatic patients displayed grade II (65.4%) and 36 displayed grade III bleeding symptoms (34.6%). First bleeding regions were skin (33%), nose (28%), central nervous system (CNS) (15.5%), oral cavity (10.5%), soft tissue (6%), joint (3%), urinary system (2%) and gastrointestinal system (GIS) (2%), respectively. The bleeding prevalence rates of our symptomatic patients are listed as epistaxis 62.5%, skin bleedings 53%, oral cavity bleeding 28.8%, haematomas 18.3%, CNS bleedings 17.3%, haemarthrosis 14.4%, GIS bleedings 3.8%, menorrhagia 2.9%, haematuria 1.9%, bleeding because of operations 1.9% and iliopsoas bleedings 1.9%. CNS bleedings (41%) take the first place among the serious bleedings of our cases, followed by haemarthrosis (36.4%), GIS bleedings (18.1%) and iliopsoas bleedings (4.5%). Prophylaxy was applied to nine patients (five patients with FVII, two patients with fibrinogen and one each with FV and FX deficiency).

CONCLUSIONS:

The characteristics of clinical presentations, first bleeding attacks, bleeding prevalence and severe bleedings as well as prophylactic approaches are discussed in this article.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos de Proteínas de Coagulação Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male / Newborn País como assunto: Asia Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transtornos de Proteínas de Coagulação Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male / Newborn País como assunto: Asia Idioma: En Ano de publicação: 2015 Tipo de documento: Article