Funato H, Inoshita N, Okeda R, Yamamoto S, Aoyagi M
Department of Neuropathology, Medical Research Institute, Tokyo Medical and Dental University, Japan.
Acta Neuropathol. 1997 Jul;94(1):95-8. doi: 10.1007/s004010050678.
Recently cases of ganglioneurocytoma and cerebral neurocytoma, very rare variants of central neurocytoma, have been reported. The former is characterized by differentiation toward ganglion cells and the latter by extraventricular origin in the cerebrum, but their existence as distinct clinicopathological entities, is controversial. We report an unusual case of neurocytoma, which arose extraventricularly from the frontal lobe, formed a large cystic lesion and showed ganglioid differentiation, in a 11-year-old girl. Following subtotal tumor resection, she showed a satisfactory clinical course and no evidence of recurrence. This is a very rare case of central neurocytoma-like tumor outside the ventricular system and also of ganglioneurocytoma. This case may provide some insight into the tumorigenesis and widen the clinicopathological concept of neurocytoma.
最近,已报道了神经节神经细胞瘤和大脑神经细胞瘤,它们是中枢神经细胞瘤非常罕见的变体。前者的特征是向神经节细胞分化,后者的特征是起源于大脑的脑室外部位,但它们作为不同的临床病理实体的存在存在争议。我们报告了一例不寻常的神经细胞瘤病例,该病例发生于一名11岁女孩的额叶脑室外,形成了一个大的囊性病变,并显示出神经节样分化。肿瘤次全切除术后,她的临床过程令人满意,且无复发迹象。这是一例非常罕见的位于脑室系统外的中枢神经细胞瘤样肿瘤病例,也是一例神经节神经细胞瘤病例。该病例可能为肿瘤发生机制提供一些见解,并拓宽神经细胞瘤的临床病理概念。