Department of Neurological Surgery, University of Wisconsin Hospitals and Clinics, Madison, WI, USA.
Department of Pathology, University of Wisconsin Hospitals and Clinics, Madison, Wisconsin.
Br J Neurosurg. 2023 Aug;37(4):601-603. doi: 10.1080/02688697.2018.1562035. Epub 2019 Feb 11.
Papillary glioneuronal tumor (PGNT) is a rare central nervous system neoplasm. Of reported cases, the vast majority are located in the frontal and temporal lobes. We present the case of a 39-year-old male who presented with a one day history of gait disturbance following chemotherapy treatment for metastatic rectal adenocarcinoma. Following MRI of the head showed a tectal mass. Following an occipital interhemispheric craniotomy for tumor resection, final pathology was diagnostic of a papillary neuroglial tumor, WHO grade I. To the best or out knowledge this is the only report of it arising from the tectal plate.
乳头状神经胶质细胞瘤(PGNT)是一种罕见的中枢神经系统肿瘤。在已报道的病例中,绝大多数位于额叶和颞叶。我们报告了 1 例 39 岁男性患者,在接受转移性直肠腺癌化疗治疗后 1 天出现步态障碍。头部 MRI 显示中脑肿块。行枕部大脑半球间开颅术切除肿瘤后,最终病理诊断为乳头状神经胶质细胞瘤,WHO 分级 I。据我们所知,这是唯一一例发生于脑桥被盖的病例。