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后颅窝的菊形团形成性胶质神经元肿瘤。

Rosette-forming glioneuronal tumors of the posterior fossa.

作者信息

Shah Manish N, Leonard Jeffrey R, Perry Arie

机构信息

Department of Neurosurgery, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

J Neurosurg Pediatr. 2010 Jan;5(1):98-103. doi: 10.3171/2009.7.PEDS09113.

Abstract

Rosette-forming glioneuronal tumor (RGNT) of the fourth ventricle is a rare, recently described WHO Grade I neoplasm. The authors report 6 examples of RGNT arising primarily from the cerebellar vermis. All the patients were female, and the mean age of presentation was 24.8 years. The original diagnoses included pilocytic astrocytoma, ependymoma, cerebellar dysembryoplastic neuroepithelial tumor (DNT), and oligodendroglioma. The cases showed classic pathological characteristics, although in 2 cases the lesions included DNT-like "floating neurons" involving Purkinje cells, a feature which has not been previously reported to the authors' knowledge. The clinical outcome was excellent with no recurrences after complete resection. These cases expand the known clinical and histological spectrum of this rare tumor type. Given the lack of fourth ventricle involvement in most of these cases, the authors suggest revising the name to RGNT of the posterior fossa.

摘要

第四脑室的菊形团形成型神经胶质神经元肿瘤(RGNT)是一种罕见的、最近才被描述的世界卫生组织一级肿瘤。作者报告了6例主要起源于小脑蚓部的RGNT。所有患者均为女性,平均发病年龄为24.8岁。最初的诊断包括毛细胞型星形细胞瘤、室管膜瘤、小脑发育异常性神经上皮肿瘤(DNT)和少突胶质细胞瘤。这些病例呈现出典型的病理特征,尽管在2例病例中,病变包含涉及浦肯野细胞的DNT样“漂浮神经元”,据作者所知,这一特征此前尚未有过报道。完全切除后临床结果极佳,无复发情况。这些病例扩展了这种罕见肿瘤类型已知的临床和组织学范围。鉴于大多数此类病例未累及第四脑室,作者建议将名称修订为后颅窝RGNT。

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