Kotecha Megha R, Singh Varsha D, Chodvadiya Surbhi A, Manade Varsha, Kamdar Gufran A
Department of Ophthalmology, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Pune, IND.
Cureus. 2024 Dec 21;16(12):e76112. doi: 10.7759/cureus.76112. eCollection 2024 Dec.
Optic nerve gliomas are tumors that develop along the optic nerve pathway, most often classified as pilocytic astrocytomas. These growths are typically benign, especially in young children between the ages of one and six years, while the rarer malignant types are generally more aggressive and tend to appear in adults. Characteristically slow-growing, optic nerve gliomas are commonly located in the pre-chiasmal part of the optic nerve but can extend to post-chiasmal regions and into the brain if left untreated. We describe a case of a one-year-old boy who visited our ophthalmology clinic with symptoms of eye prominence and deviation in his right eye after undergoing chemotherapy. Clinical findings and additional assessments supported an optic nerve glioma diagnosis. This case underlines the significance of early detection and a collaborative approach among ophthalmologists, neurosurgeons, radiologists, and histopathologists for effective management and to limit disease progression.
视神经胶质瘤是沿着视神经通路发展的肿瘤,最常被归类为毛细胞型星形细胞瘤。这些肿瘤通常是良性的,尤其是在1至6岁的幼儿中,而较罕见的恶性类型通常更具侵袭性,且往往出现在成年人中。视神经胶质瘤的特点是生长缓慢,通常位于视神经的视交叉前部分,但如果不治疗,可延伸至视交叉后区域并进入大脑。我们描述了一例1岁男孩的病例,该男孩在接受化疗后因右眼突出和斜视症状前来我们的眼科诊所就诊。临床检查结果和其他评估支持视神经胶质瘤的诊断。该病例强调了早期检测以及眼科医生、神经外科医生、放射科医生和组织病理学家之间采取协作方法对于有效管理和限制疾病进展的重要性。