The circumstances of diagnosis of occult haemophilia B in a patient with severe maxillofacial injuries

Autor

  • Joanna Wojnar Clinical Ward of Maxillofacial Surgery, Provincial Specialist Hospital in Rzeszow, Poland Autor
  • Bogumił Lewandowski Clinical Ward of Maxillofacial Surgery, Provincial Specialist Hospital in Rzeszow, Poland; Chair of Emergency Medicine, Faculty of Medicine Rzeszow University, Poland Autor
  • Mateusz Dymek Clinical Ward of Maxillofacial Surgery, Provincial Specialist Hospital in Rzeszow, Poland Autor
  • Dorota Ozga Chair of Emergency Medicine, Faculty of Medicine Rzeszow University, Poland Autor
  • Małgorzata Migut Clinical Ward of Maxillofacial Surgery, Provincial Specialist Hospital in Rzeszow, Poland Autor

DOI:

https://doi.org/10.12923/j.2084-980X/26.1/a.21

Słowa kluczowe:

fractures, maxillofacial injury, inherited bleeding discorders, haemophilia B

Abstrakt

The most common haemostasis disorders are haemophilia A, B and von Willebrand disease. Symptoms of congenital bleeding diathesis can be observed in early childhood, and are easy to recognize. Medical literature describes cases of late diagnosis of haemostasis disorders. These cases are usually detected accidentally, and they can present a serious diagnostic and therapeutic problem. In this article, the authors describe a patient with massive maxillofacial trauma in whom a haemostasis disorder was detected and diagnosed as haemophilia B. Detection of this disorder was of significant importance for the treatment of the primary disease, i.e. maxillofacial injuries.

Bibliografia

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Opublikowane

2013-03-29

Jak cytować

Wojnar, J., Lewandowski, B., Dymek, M., Ozga, D., & Migut, M. (2013). The circumstances of diagnosis of occult haemophilia B in a patient with severe maxillofacial injuries. Current Issues in Pharmacy and Medical Sciences, 26(1), 99-101. https://doi.org/10.12923/j.2084-980X/26.1/a.21