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神经纤维瘤病。第1部分:NF1

The Neurofibromatoses. Part 1: NF1.

作者信息

Lu-Emerson Christine, Plotkin Scott R

机构信息

Department of Neurology, University of Washington, Seattle, WA, USA.

出版信息

Rev Neurol Dis. 2009 Spring;6(2):E47-53.

Abstract

The neurofibromatoses, including neurofibromatosis 1 (NF1), neurofibromatosis 2 (NF2), and schwannomatosis, comprise a group of genetically distinct disorders of the nervous system unified by the predisposition to nerve sheath tumors. NF1 is the most common neurogenetic disorder, with a birth incidence of 1 in 3000. NF1 is inherited in auto-somal dominant fashion with full penetrance and variable expressivity. The hallmark lesion of NF1 is the neurofibroma, a benign tumor derived from the nerve sheath and composed of a mixture of proliferating Schwann cells, fibroblasts, mast cells, and pericytes. Other findings include gliomas, learning disability, vasculopathy, and bony abnormalities. Café au lait macules are typically the initial clinical manifestation of NF1 and tend to increase in size and number throughout childhood and puberty. Current treatment of patients with NF1 remains primarily surgical. Genetic counseling is essential for adult patients because molecular diagnostic testing can minimize the risk of transmission to children.

摘要

神经纤维瘤病,包括神经纤维瘤病1型(NF1)、神经纤维瘤病2型(NF2)和施万细胞瘤病,是一组由神经系统遗传特征不同的疾病组成的疾病,其共同特点是易患神经鞘瘤。NF1是最常见的神经遗传性疾病,出生发病率为1/3000。NF1以常染色体显性方式遗传,具有完全外显率和可变表达性。NF1的标志性病变是神经纤维瘤,这是一种起源于神经鞘的良性肿瘤,由增殖的施万细胞、成纤维细胞、肥大细胞和周细胞混合组成。其他表现包括胶质瘤、学习障碍、血管病变和骨骼异常。牛奶咖啡斑通常是NF1的初始临床表现,在整个儿童期和青春期往往会增大且数量增多。目前NF1患者的治疗主要仍是手术治疗。对于成年患者,遗传咨询至关重要,因为分子诊断检测可以将遗传给儿童的风险降至最低。

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