Hosoya Tomohiro, Kambe Atsushi, Miyamoto Daiou, Sakamoto Makoto, Kurosaki Masamichi
Division of Neurosurgery, Department of Brain and Neurosciences, School of Medicine, Faculty of Medicine, Tottori University, Yonago 683-8503, Japan.
Yonago Acta Med. 2023 Jul 22;66(3):385-388. doi: 10.33160/yam.2023.08.006. eCollection 2023 Aug.
Papillary glioneuronal tumor (PGNT) is a low-grade biphasic tumor that is composed of glial fibrillary acidic protein (GFAP)-positive glial cells and synaptophysin-positive neurons. We report a case of PGNT occurring in the right occipital lobe of a 48-year-old woman who presented with acute headache and left homonymous hemianopsia, the latter of which was difficult to distinguish from malignant brain tumors because of peritumoral brain edema, intratumoral hemorrhage, and intraoperative fluorescence staining. PGNT should be included as one of the differential diagnoses in cases where the tumor shows hemorrhagic change despite decreased perfusion in arterial spin labeling MRI.
乳头状胶质神经元肿瘤(PGNT)是一种低级别双相性肿瘤,由胶质纤维酸性蛋白(GFAP)阳性的胶质细胞和突触素阳性的神经元组成。我们报告一例发生在一名48岁女性右枕叶的PGNT病例,该患者表现为急性头痛和左侧同向性偏盲,由于瘤周脑水肿、瘤内出血和术中荧光染色,后者难以与恶性脑肿瘤区分。在动脉自旋标记磁共振成像中尽管灌注降低但肿瘤出现出血改变的病例中,PGNT应作为鉴别诊断之一。