1型神经纤维瘤病伴面神经纤维瘤的颅内异常。

Neurofibromatosis Pub Date : 1989-01-01
E Boltshauser, H Stocker, H Sailer, A Valavanis
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引用次数: 0

摘要

从1975年到1988年,我们研究了17例1型神经纤维瘤病和毁容性面神经纤维瘤(FPN)。13例患者FPN偏左。4人是眼眶/眶周,7人是下面部6人是整张脸。神经影像学(n = 13)显示8例为肿瘤(视神经通路或基底神经节),2例为同侧颅中窝蛛网膜囊肿,1例为多发高信号区(t2加权磁共振成像),2例为正常。NF-1合并FPN的患者颅内肿瘤和蛛网膜囊肿的发生率似乎很高。我们的观察结果必须在更大的患者系列中得到证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intracranial abnormalities associated with facial plexiform neurofibromas in neurofibromatosis type 1.

From 1975 to 1988 seventeen patients with neurofibromatosis type 1 and a disfiguring facial plexiform neurofibroma (FPN) were investigated. The FPN was left-sided in 13 patients. It was orbital/periorbital in 4, lower facial in 7 and involved the whole face in 6 subjects. Neuroimaging (n = 13) revealed a tumor (of optic pathways or basal ganglia) in 8, an ipsilateral middle cranial fossa arachnoid cyst in 2, multiple areas of high signal intensity (in T2-weighted magnetic resonance imaging) in 1, and normal findings in 2 patients. In NF-1 patients with FPN there seems to be a high incidence of intracranial tumors and possibly of arachnoid cysts. Our observation has to be confirmed in a larger patient series.

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