Alshantti Khalilalrahman, Nadarajan Chandran, Mijol Mitchell Modi, Mat Zin Anani Aila
Department of Radiology, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, Kubang Kerian, MYS.
Department of Pathology, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, Kubang Kerian, MYS.
Cureus. 2022 Mar 11;14(3):e23060. doi: 10.7759/cureus.23060. eCollection 2022 Mar.
Pleomorphic xanthoastrocytoma (PXA) is a rare glioma that affects 1% of astrocytic tumors. It most commonly affects children and teenagers. PXA cases with an anaplastic histopathological subtype have been reported in recent years. It was recently classified as a separate subtype in the 2016 World Health Organization (WHO) classification of central nervous system (CNS) tumors. A 48-year-old healthy gentleman presented with progressive right upper limb weakness. CT and MRI of the brain were done, which showed an intra-axial supratentorial tumor. A diagnosis of high-grade glioma was initially made based on its imaging features. The histopathological study came back as anaplastic pleomorphic xanthoastrocytoma. After a discussion with the neurosurgical and oncology teams, a decision was made to treat the patient with radiotherapy. In this case report, we describe a rare case of PXA with anaplastic characteristics.
多形性黄色瘤型星形细胞瘤(PXA)是一种罕见的胶质瘤,占星形细胞肿瘤的1%。它最常影响儿童和青少年。近年来已报道了具有间变性组织病理学亚型的PXA病例。它最近在2016年世界卫生组织(WHO)中枢神经系统(CNS)肿瘤分类中被列为一个单独的亚型。一名48岁的健康男性出现进行性右上肢无力。进行了脑部CT和MRI检查,显示为幕上脑内肿瘤。最初根据其影像学特征诊断为高级别胶质瘤。组织病理学研究结果为间变性多形性黄色瘤型星形细胞瘤。在与神经外科和肿瘤学团队讨论后,决定对该患者进行放射治疗。在本病例报告中,我们描述了一例具有间变性特征的罕见PXA病例。