Chen Fan, Jin Rihua, Wu Xinmin, Dong Zengping, Chen Dawei
Department of Neurosurgery, First Hospital of Jilin University, Changchun, China.
Department of Neurosurgery, First Hospital of Jilin University, Changchun, China.
World Neurosurg. 2018 Apr;112:178-181. doi: 10.1016/j.wneu.2018.01.104. Epub 2018 Feb 22.
Neurocytoma is a rare brain neoplasm of neuroepithelial origin that occurs predominantly in the ventricular system adjacent to the interventricular foramen and septum pellucidum. However, extraventricular neurocytoma is an extremely rare entity, with poor clinical, radiologic, and histopathological characterization. Here we report a case of an extraventricular parafalcine neurocytoma in the left frontal lobe. We also examine previously reported cases of extraventricular neurocytoma in an attempt to provide an up-to-date summary of the condition.
A literature search was performed using PubMed with specific key terms, inclusion criteria, and exclusion criteria. Selected case studies and case series were then compared, and statistical analyses were performed where appropriate. We report a 59-year-old woman presenting with weakness in her right leg and urinary incontinence. Physical examination revealed muscle strength of grade 3/5 in the right lower extremity. Brain magnetic resonance imaging showed a parafalcine mass in the left frontal lobe, with perilesional edema; the cerebral falx and lateral ventricle were shifted due to the compression. Gross total resection was performed.
Histopathological examination revealed a neurocytoma. Immunohistochemical staining showed diffuse positivity for synaptophysin. MIB-1 staining for Ki-67 antibody showed a labeling index of 20%. No adjuvant radiation or chemotherapy was administered. Brain computed tomography performed at a 3-month follow-up showed no signs of recurrence.
Extraventricular neurocytoma occurring in the brain parenchyma is a very rare central nervous system tumor. Its clinical and radiologic manifestations are nonspecific. The diagnosis depends on histopathological and immunohistochemical examination. Surgical resection should be the first-choice treatment.
神经细胞瘤是一种罕见的神经上皮源性脑肿瘤,主要发生在与室间孔和透明隔相邻的脑室系统。然而,脑室外神经细胞瘤是一种极其罕见的实体,其临床、放射学和组织病理学特征较差。在此,我们报告一例左侧额叶脑室外大脑镰旁神经细胞瘤病例。我们还研究了先前报道的脑室外神经细胞瘤病例,试图提供该病症的最新总结。
使用PubMed进行文献检索,设定了特定的关键词、纳入标准和排除标准。然后对选定的病例研究和病例系列进行比较,并在适当情况下进行统计分析。我们报告一名59岁女性,出现右腿无力和尿失禁症状。体格检查发现右下肢肌力为3/5级。脑部磁共振成像显示左侧额叶大脑镰旁有一肿块,伴有瘤周水肿;大脑镰和侧脑室因受压而移位。进行了全切除手术。
组织病理学检查显示为神经细胞瘤。免疫组化染色显示突触素弥漫阳性。Ki-67抗体的MIB-1染色显示标记指数为20%。未给予辅助放疗或化疗。术后3个月的脑部计算机断层扫描显示无复发迹象。
发生于脑实质的脑室外神经细胞瘤是一种非常罕见的中枢神经系统肿瘤。其临床和放射学表现不具有特异性。诊断依赖于组织病理学和免疫组化检查。手术切除应作为首选治疗方法。