Hemophilia C in maxillofacial surgery – A rare finding

S. Vasudev, Shreya Singh, M. Sahana, J. K. Jacob
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Abstract

Factor XI (FXI) deficiency or hemophilia C is a very rare, autosomal recessive bleeding disorder. Patients with this deficiency do not typically show spontaneous bleeding or any specific symptoms. Those who have this disorder are seldom identified during situations such as trauma or surgery or during pre-surgical workups. Hence, operating on such patients, especially those with intraoral or vascular tumors, is particularly associated with a high bleeding risk. Therefore, great care must be taken when treating patients with disorders such as FXI deficiency. There are very few reports that address the management of patients with bleeding disorders in maxillofacial vascular lesions. Here, we report a patient with FXI deficiency, who underwent surgical excision of pyogenic granuloma of her upper right alveolus under general anesthesia and describe all the measures taken to reduce the chances of excessive bleeding.
颌面部外科血友病C -一个罕见的发现
这种缺乏症的患者通常不会出现自发性出血或任何特殊症状。那些患有这种疾病的人很少在创伤或手术或术前检查等情况下被发现。因此,对这类患者进行手术,特别是那些有口腔内或血管肿瘤的患者,尤其与出血的高风险相关。因此,在治疗FXI缺乏症等疾病的患者时,必须非常小心。关于颌面部血管病变并发出血性疾病的处理报道很少。在这里,我们报告了一位FXI缺乏的患者,她在全身麻醉下接受了右上肺泡化脓性肉芽肿的手术切除,并描述了所有采取的措施来减少出血的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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