Juvenile nasopharyngeal angiofibroma

被引:0
|
作者
Tewfik, TL [1 ]
Tan, AKW [1 ]
Al Noury, K [1 ]
Chowdhury, K [1 ]
Tampieri, D [1 ]
Raymond, J [1 ]
Vuong, T [1 ]
机构
[1] McGill Univ, Dept Otolaryngol, Montreal, PQ, Canada
来源
JOURNAL OF OTOLARYNGOLOGY | 1999年 / 28卷 / 03期
关键词
angiofibroma; juvenile; nasopharyngeal;
D O I
暂无
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
This is a retrospective study of 17 patients with juvenile nasopharyngeal angiofibroma treated from 1983 to 1996. Patients with Stage I or II disease according to the Fisch classification system were treated surgically by a transpalatal approach. One patient underwent a Le Fort I osteotomy and down-fracture approach for access. Three patients underwent combined transpalatal and lateral rhinotomy far access, whereas one underwent a transcervical double mandibular osteotomy to facilitate the exposure. A patient with Stage IV disease underwent a combined subcranial frontonasal osteotomy plus a Le Fort I osteotomy for access to a massive angiofibroma. Initial surgical management prevented recurrence in 79% of patients. Two patients with intracranial extension were treated with primary irradiation therapy; their tumours became asymptomatic. Preoperative angiography and embolization were used to treat all surgical candidates. The use of newer craniofacial or subcranial techniques and infratemporal fossa approaches with osteotomies can provide access to large angiofibromas even when there is skull base or intracranial involvement. Surgical exposure may also be enhanced by the use of the Le Fort I osteotomy and down-fracture approaches.
引用
收藏
页码:145 / 151
页数:7
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