Menius J W, Webster W P
Oral Surg Oral Med Oral Pathol. 1978 May;45(5):714-20. doi: 10.1016/0030-4220(78)90146-9.
Classic hemophilia (hemophilia A. Factor VIII deficiency, antihemophilic factor deficiency) and polycythemia vera were diagnosed in a patient who presented for management of his dental disease. This case report summarizes the history, laboratory findings, and clinical course and discusses the various diagnostic considerations in the management of two rare disorders. A review of current concepts of hemophilia and polycythemia vera is presented.
一名因牙科疾病前来治疗的患者被诊断出患有典型血友病(血友病A、凝血因子VIII缺乏症、抗血友病因子缺乏症)和真性红细胞增多症。本病例报告总结了病史、实验室检查结果和临床病程,并讨论了这两种罕见疾病治疗中的各种诊断考量因素。文中还介绍了血友病和真性红细胞增多症的当前概念。