AAssar O S, Friedman C M, White R I
Department of Diagnostic Radiology, Yale University School of Medicine, New Haven, Conn.
Laryngoscope. 1991 Sep;101(9):977-80. doi: 10.1288/00005537-199109000-00008.
The purpose of this retrospective study is to document the natural history of epistaxis in patients with hereditary hemorrhagic telangiectasia. A telephone questionnaire was administered to 73 patients who had been previously screened for pulmonary arteriovenous malformations (PAVMs). The incidence of epistaxis in this population was 93%, with a mean onset age of epistaxis of 12 years, a mean frequency of bleeding of 18 episodes per month, and a mean duration of bleeding of 7.5 minutes. More than 90% of patients experienced the onset of epistaxis before the age of 21 and symptoms were progressive with age. There were no differences in the age of onset, frequency of epistaxis, or duration of epistaxis between patients with PAVMs versus those without PAVMs. Although the natural history of epistaxis does not predict the presence or absence of pulmonary arteriovenous malformations, epistaxis is an early marker of the disease, hereditary hemorrhagic telangiectasia, and might guide screening for pulmonary and cerebral arteriovenous malformations in children of affected parents.
这项回顾性研究的目的是记录遗传性出血性毛细血管扩张症患者鼻出血的自然病史。对73名先前已接受肺动静脉畸形(PAVM)筛查的患者进行了电话问卷调查。该人群中鼻出血的发生率为93%,鼻出血的平均发病年龄为12岁,平均出血频率为每月18次,平均出血持续时间为7.5分钟。超过90%的患者在21岁之前出现鼻出血,且症状随年龄增长而加重。有PAVM的患者与无PAVM的患者在鼻出血的发病年龄、频率或持续时间方面没有差异。虽然鼻出血的自然病史不能预测肺动静脉畸形的有无,但鼻出血是该疾病——遗传性出血性毛细血管扩张症的早期标志,可能有助于指导对患病父母的子女进行肺和脑动静脉畸形的筛查。