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1型神经纤维瘤病患者视交叉前胶质瘤表现的特异性:眼科和神经影像学方面

[Specific features of manifestation of anterior optic tract gliomas in patients with type 1 neurofibromatosis: ophthalmological and neurovisualizational aspects].

作者信息

Serova N K, Lazareva L A, Ozerova V I, Pronin I N, Gorelychev S K

出版信息

Vestn Oftalmol. 2006 Nov-Dec;122(6):36-9.

Abstract

Gliomas of the anterior optic tract (AOT) (optic nerves, chiasms, and visual tracts) are benign slowly growing tumors usually detectable in childhood. These are a rather heterogenic group of tumors. The pattern and course of the disease are frequently affected by the presence of type 1 neurofibromatosis (NF-1) in the patient. The ophthalmological symptoms of AOT lesion in the presence of NF-1 were analyzed in 80 patients aged 1 to 24 years (median 5 years). According to the ophthalmological symptoms and the pattern and extent of lesions to AOT structures, the authors identified 4 groups by the data of neurovisualization techniques (magnetic resonance imaging, computed tomography) and revealed that the ophthalmological pattern reflected the site and degree of lesion to AOT structures. At the same time it is shown that there is a group of silent tumors attending without visual disorders. These tumors have the similar neurovisualization pattern, such as a moderate thickening of AOT structures and they occur in 13.8% of cases, as shown by the authors.

摘要

前视路(AOT)(视神经、视交叉和视束)胶质瘤是良性的、生长缓慢的肿瘤,通常在儿童期可被发现。这些肿瘤是一组相当异质性的肿瘤。疾病的模式和进程常常受到患者是否存在1型神经纤维瘤病(NF-1)的影响。对80名年龄在1至24岁(中位年龄5岁)的患者中存在NF-1时AOT病变的眼科症状进行了分析。根据眼科症状以及AOT结构病变的模式和范围,作者通过神经可视化技术(磁共振成像、计算机断层扫描)的数据确定了4组,并发现眼科模式反映了AOT结构的病变部位和程度。同时表明,有一组无症状肿瘤,不伴有视觉障碍。这些肿瘤具有相似的神经可视化模式,如AOT结构中度增厚,作者指出,此类肿瘤在病例中占13.8%。

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