Intracranial visual pathway gliomas in children with neurofibromatosis.

Neurofibromatosis Pub Date : 1988-01-01
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Abstract

The association between neurofibromatosis and visual pathway gliomas is well documented. The introduction of computed tomography and magnetic resonance imaging has heralded a new era in the understanding of visual pathway gliomas. Both of these noninvasive neuroinvestigative techniques have demonstrated extensive abnormalities throughout the visual pathway in children with visual pathway gliomas, especially in those with neurofibromatosis. The clinical significance of these abnormal areas of brain, especially in asymptomatic patients, is unknown. In an attempt to clarify the incidence, natural history, and clinical course of patients with neurofibromatosis and visual pathway lesions, we reviewed our experience with 24 patients managed consecutively at Children's Hospital of Philadelphia over the past 12 years. The patients in this series were compared to 29 children with visual pathway gliomas without neurofibromatosis who were evaluated at our institution over the same period of time. Visual pathway gliomas in children with neurofibromatosis differ from those in children without neurofibromatosis. In general, lesions tended to be more extensive in patients with neurofibromatosis and the clinical course of these patients is more variable. Twelve of the 24 patients with neurofibromatosis in our series had symptoms of progressive disease at the time of diagnosis and underwent treatment with variable results. Twelve children with neurofibromatosis and visual pathway lesions had static lesions at the time of diagnosis and, to date, 3 have developed progressive disease. From our review we can make some recommendations concerning the management of children with neurofibromatosis and visual pathway gliomas, but many questions remain unanswered. Sequential follow-up of a large cohort of both asymptomatic and symptomatic children with neurofibromatosis and visual pathway lesions is needed to more definitively outline the best management approach for these patients.

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神经纤维瘤病患儿颅内视通路胶质瘤。
神经纤维瘤病和视觉通路胶质瘤之间的关系是有充分证据的。计算机断层扫描和磁共振成像的引入预示着对视觉通路胶质瘤的理解进入了一个新的时代。这两种非侵入性神经调查技术都显示了视觉通路中广泛的异常,特别是在那些患有神经纤维瘤病的儿童中。这些大脑异常区域的临床意义,特别是在无症状患者中,尚不清楚。为了阐明神经纤维瘤病和视觉通路病变患者的发病率、自然病史和临床病程,我们回顾了过去12年来在费城儿童医院连续治疗的24例患者的经验。该系列患者与29名在同一时期在我们机构接受评估的无神经纤维瘤病的视觉通路胶质瘤儿童进行了比较。神经纤维瘤病儿童的视通路胶质瘤不同于非神经纤维瘤病儿童。一般来说,神经纤维瘤病患者的病变往往更广泛,这些患者的临床病程也更多变。在我们的研究中,24例神经纤维瘤病患者中有12例在诊断时有进行性疾病的症状,并接受了不同结果的治疗。12名患有神经纤维瘤病和视觉通路病变的儿童在诊断时为静态病变,迄今为止,3名已发展为进行性疾病。从我们的综述中,我们可以对神经纤维瘤病和视觉通路胶质瘤患儿的治疗提出一些建议,但许多问题仍未得到解答。需要对大量无症状和有症状的神经纤维瘤病和视觉通路病变儿童进行序贯随访,以更明确地概述这些患者的最佳治疗方法。
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Optic Pathway Gliomas Exposure of newborn mice to adenosine causes neural crest dysplasia and tumor formation. Summary of patient data from a multidisciplinary neurofibromatosis clinic. Hemimegalencephaly, hemifacial hypertrophy and intracranial lipoma: a variant of neurofibromatosis. Neurofibromatosis in Gothenburg, Sweden. II. Intellectual compromise.
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