Konar Subhas K, Shukla Dhaval, Nandeesh Bevinahalli Nanjegowda, Prabhuraj Andiperumal Raj, Devi B Indira
Department of Neurosurgery, National Institute of Mental Health and Neurosciences, Bangalore, India,
Department of Neurosurgery, National Institute of Mental Health and Neurosciences, Bangalore, India.
Pediatr Neurosurg. 2019;54(2):139-142. doi: 10.1159/000495990. Epub 2019 Jan 24.
The incidence of bilateral thalamic glioma in children is not reported in the literature. The majority of cases comprise either diffuse astrocytoma, anaplastic astrocytoma, or glioblastoma. Partial surgical resection or biopsy followed by adjuvant therapy is the usual treatment for bilateral thalamic gliomas. Prognosis is dependent on tumor grade and extent of tumor spread to surrounding critical structures. We present a rare case of bilateral thalamic pilocytic astrocytoma. Endoscopic biopsy, septostomy, and placement of a ventriculoperitoneal shunt was done followed by radiotherapy. The 36-month follow-up demonstrated radiological control of the tumor.
儿童双侧丘脑胶质瘤的发病率在文献中未见报道。大多数病例为弥漫性星形细胞瘤、间变性星形细胞瘤或胶质母细胞瘤。双侧丘脑胶质瘤的常规治疗是部分手术切除或活检,然后进行辅助治疗。预后取决于肿瘤分级以及肿瘤扩散至周围关键结构的程度。我们报告一例罕见的双侧丘脑毛细胞型星形细胞瘤病例。进行了内镜活检、造瘘术及脑室腹腔分流术,随后进行放疗。36个月的随访显示肿瘤得到影像学控制。