青少年鼻咽血管纤维瘤——原发性眼眶发育的罕见病例。
Juvenile nasopharyngeal angiofibroma--a rare case of primary orbital development.
作者信息
Moschos M, Demetra A, Kontogeorgos G
机构信息
Ophthalmology Department, University of Athens, Greece.
出版信息
Acta Ophthalmol Scand. 1998 Aug;76(4):506-8. doi: 10.1034/j.1600-0420.1998.760423.x.
PURPOSE
To present a rare case of juvenile nasopharyngeal angiofibroma invading the ophthalmic orbit.
METHODS
The CT scan examination and the ultrasound tomography revealed the existence of a homogeneous solid mass causing distention and erosion of the nasal wall as well as dislocation of the ocular bulbus.
RESULT
The patient was operated, the mass was carefully liberated from its synechiae and it was totally excised with its capsule.
CONCLUSION
A rare case of juvenile nasopharyngeal angiofibroma invading the orbit is presented. The tumor was totally excized and the patient is five years after the operation in good general health without recurrence of the tumor.
目的
报告1例罕见的侵犯眼眶的青少年鼻咽血管纤维瘤病例。
方法
CT扫描检查和超声断层扫描显示存在一个均匀的实性肿块，导致鼻壁膨隆和侵蚀以及眼球移位。
结果
患者接受了手术，肿块从粘连处小心分离，并连同包膜一起完整切除。
结论
报告了1例罕见的侵犯眼眶的青少年鼻咽血管纤维瘤病例。肿瘤被完整切除，患者术后5年总体健康状况良好，肿瘤无复发。
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