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J Pediatr Hematol Oncol ; 43(4): e561-e563, 2021 05 01.
Artigo em Inglês | MEDLINE | ID: mdl-32769563

RESUMO

A 16-year-old boy with severe hemophilia B and minimal bleeding manifestations in his early childhood presented with gastrointestinal bleeding at 11 years of age. Following administration of prothrombin complex concentrate, he developed peripheral venous thrombosis and cerebral sinovenous thrombosis, posing a management dilemma. His cerebral sinovenous thrombosis resolved spontaneously, proving watchful waiting to be a useful strategy. He developed spontaneous intracranial bleed at 14 years of age for which he was treated with factor IX concentrate and commenced on prophylaxis. We discuss the factors contributing to genotype-phenotype dissonance in severe hemophilia and considerations before commencing prophylaxis in such cases.


Assuntos
Fatores de Coagulação Sanguínea/uso terapêutico , Fator IX/uso terapêutico , Hemofilia B/terapia , Hemorragia/terapia , Trombose/etiologia , Adolescente , Fatores de Coagulação Sanguínea/efeitos adversos , Humanos , Masculino
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