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临床资料 一般资料 男2例,女5例。年龄9～62岁,平均39岁。病程7月至7年,平均27.3月。 临床表现 头痛6例,视力减退5例(为首发症状),视乳头水肿6例,眼球突出伴Ⅲ、Ⅳ、Ⅵ颅神经损害1例,偏瘫2例,癫痫发作2例(1例首发症状),面部感觉减退1例,幻嗅1例,表情淡漠1例,记忆力减退3例。 辅助检查 7例均行头颅正侧位片,发现骨质增生、破坏、吸收6例,分别有不同程度蝶骨嵴、岩骨尖、颞骨、蝶鞍区及前、中颅底骨质浸润。7例均行CT扫描示:蝶骨嵴部边界清楚,高密度、不同程度增强的占位病变。其中1例向中线对侧生
General information on clinical data 2 males and 5 females. Aged 9 to 62 years old, average 39 years old. Duration of July to 7 years, an average of 27.3 months. Clinical manifestations of headache in 6 cases, 5 cases of vision loss (as the first symptom), papilledema in 6 cases, prominent with Ⅲ, Ⅳ, Ⅵ cranial nerve injury in 1 case, 2 cases of hemiplegia, epileptic seizures in 2 cases (1 case of first symptom) , Facial sensation in 1 case, phantom sniff in 1 case, apathy in 1 case, memory loss in 3 cases. Auxiliary examination of 7 cases were performed cephalometric films and found bone hyperplasia, destruction, absorption in 6 cases, respectively, with varying degrees of sphenoid ridge, petrous apex, temporal bone, sella region and anterior and middle skull base bone infiltration. Seven cases of CT scan showed: sphenoid ridge border clear, high density, varying degrees of enhanced space-occupying lesions. One case of midline contralateral students