Oral surgery for combined haemophilia A and B. The dos and don’ts presented in a clinical scenario

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Madalina Anca Lazar
Ovidiu Muresan
Calin Rares Roman
Delia Dima
Mihai Stefan Muresan
Gabriel Armencea
Ciprian Tomuleasa
Horatiu Rotaru

Abstract





BACKGROUND: Haemophilia A (factor VIII deficiency), B (factor IX deficiency) and C (factor XI deficiency) are com- mon genetic bleeding disorders. Most often they are caused by the absence or defective function of coagulation factors, causing inefficient blood clots.


CASE REPORT: The present manuscript describes a rare case of a combined haemophilia A and B patient, who under- went several extractions. The therapy and clinical management is presented, in the view of surgeon as well as haema- tologist.


CONCLUSION: These patients are a serious challenge for the oral surgeons due to an increased number of accidents and complications. Scarce literature covering this topic contributes, as well, to the difficult management. Thus, several prin- ciples must be considered when diagnosing and treating haemophilia patients.





Article Details

How to Cite
Madalina Anca Lazar, et al. “Oral Surgery for Combined Haemophilia A and B. The Dos and don’ts Presented in a Clinical Scenario”. Annali Italiani Di Chirurgia, vol. 89, no. 5, Sept. 2018, pp. 374-8, https://annaliitalianidichirurgia.it/index.php/aic/article/view/1124.
Section
Case Report