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伴有双侧听神经瘤的中枢性神经纤维瘤病:与周围性神经纤维瘤病在遗传、临床及生化方面的差异

Central neurofibromatosis with bilateral acoustic neuroma: genetic, clinical and biochemical distinctions from peripheral neurofibromatosis.

作者信息

Kanter W R, Eldridge R, Fabricant R, Allen J C, Koerber T

出版信息

Neurology. 1980 Aug;30(8):851-9. doi: 10.1212/wnl.30.8.851.

Abstract

Neurofibromatosis includes the common "peripheral" form and a recently documented "central" form. We describe the central form in 130 cases from 9 kindreds personally studied and 15 reported kindreds. Central neurofibromatosis with bilateral acoustic neuroma is an autosomal dominant disorder beginning about 20 years of age, accompanied by mild skin changes. In three kindreds with central neurofibromatosis, we measured nerve growth factor in serum by radioimmunoassay and radioreceptor assay. Only the antigenic activity of nerve growth factor was increased. In contrast, in peripheral neurofibromatosis, only the functional activity of nerve growth factor has been reported increased. Central and peripheral forms of neurofibromatosis are closely related but discrete diseases which appear to have separate alterations in nerve growth factor activity.

摘要

神经纤维瘤病包括常见的“外周型”和最近记录的“中枢型”。我们描述了来自9个家系的130例个人研究病例和15个已报道家系中的中枢型。双侧听神经瘤的中枢神经纤维瘤病是一种常染色体显性疾病,发病年龄约为20岁,伴有轻度皮肤改变。在三个患有中枢神经纤维瘤病的家系中,我们通过放射免疫测定和放射受体测定法测量了血清中的神经生长因子。仅神经生长因子的抗原活性增加。相比之下,在外周神经纤维瘤病中,仅报道神经生长因子的功能活性增加。神经纤维瘤病的中枢型和外周型密切相关但却是不同的疾病,它们在神经生长因子活性方面似乎有不同的改变。

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