Surgical experience of a rare ventricular tumor: A case report

Hyeon Gyu Yang, Joonho Byun, Sang Woo Song, Young-Hoon Kim, Chang Ki Hong, Jeong Hoon Kim
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Abstract

In this case report, we present a rare case of a suspicious central nervous system (CNS) high-grade neuroepithelial tumor with BCOR alteration (CNS HGNET-BCOR). A 29-year-old woman ini-tially presented with an incidental ventricular tumor detected on computed tomography. The brain magnetic resonance imaging revealed a 6 × 5 cm heterogeneously enhancing solid cystic mass with coarse calcifications in the right lateral ventricle. Preoperative radiological diagnosis suggested a cen-tral neurocytoma, and subsequent surgery was done in gross total resection with satisfactory recov-ery. However, after three years, tumor recurrence was observed, leading to revision surgery. Based on the histopathological evaluation according to the 2021 World Health Organization classification, the tumor was suggested as CNS HGNET-BCOR. Adjuvant radiotherapy was planned as part of the treatment strategy. This case report contributes to the limited knowledge about intraventricular CNS HGNET-BCOR tumors, offering insights into diagnosis and treatment approaches for this rare en-tity.
罕见脑室肿瘤的手术治疗经验1例
在本病例报告中,我们报告一例可疑的中枢神经系统(CNS)高级别神经上皮肿瘤伴BCOR改变(CNS HGNET-BCOR)的罕见病例。一位29岁的女性最初在计算机断层扫描上发现了一个偶然的脑室肿瘤。脑磁共振示右侧侧脑室一6 × 5 cm不均质强化实性囊性肿块伴粗钙化。术前影像学诊断为中枢神经细胞瘤,术后行大体全切除,恢复满意。然而,三年后,观察到肿瘤复发,导致翻修手术。根据世界卫生组织2021年分类进行组织病理学评估,建议肿瘤为中枢神经系统HGNET-BCOR。辅助放疗计划作为治疗策略的一部分。本病例报告有助于对脑室内中枢神经系统HGNET-BCOR肿瘤的有限认识,为这种罕见肿瘤的诊断和治疗方法提供见解。
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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