A Rare Case of Sporadic Optic Pathway Glioma in a 7-year-old Female.

Q4 Medicine
Kathmandu University Medical Journal Pub Date : 2024-10-01
S Gupta, U Sinha, A Raj
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引用次数: 0

Abstract

Sporadic optic pathway gliomas (OPGs) are uncommon and have greater predisposition to severe clinical presentations and complications. Severe visual impairment is the most frequent presentation. The treatment is based on multiple factors and needs to be individualized. Precise assessment of visual function is one of the important factors to plan the management. We present a case of sporadic OPG in a 7-year-old female with severe visual decline. Visual functions were assessed ophthalmologically and electrophysiologically. Diagnosis was confirmed on the basis of clinical, radiological, histopathological and electrophysiologic findings. Surgical resection was planned owing to the poor visual functions and the mass effects. Patient is on regular follow-ups with no signs of deterioration so far. Appropriate visual assessment is crucial in young children with sporadic optic pathway glioma for planning the mode of treatment. Surgical resection in cases with severe visual impairment is helpful, however, irreversible visual impairment remains irremediable.

罕见的散发性视神经通路胶质瘤1例7岁女性。
散发性视神经胶质瘤(OPGs)是罕见的,有更大的倾向于严重的临床表现和并发症。严重视力障碍是最常见的表现。治疗是基于多种因素,需要个性化。准确的视觉功能评估是制定治疗计划的重要因素之一。我们提出一例散发性OPG在一个7岁的女性严重视力下降。用眼生理学和电生理学方法评估视功能。诊断依据临床、放射学、组织病理学和电生理检查结果。因视力差及肿块影响,计划手术切除。病人正在定期随访,到目前为止没有恶化的迹象。对于散发性视神经胶质瘤的幼儿,适当的视觉评估对于规划治疗模式至关重要。手术切除严重视力损害的病例是有帮助的,然而,不可逆的视力损害仍然是不可补救的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Kathmandu University Medical Journal
Kathmandu University Medical Journal Medicine-Medicine (all)
CiteScore
0.70
自引率
0.00%
发文量
51
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