Department of Basic Medical Sciences, Faculty of medicine, Yarmouk University, Irbid, Jordan.
Department of Radiological, Oncological & Anatomopathological Sciences, Sapienza University of Rome, Rome, Italy.
CNS Oncol. 2020 Jun;9(2):CNS54. doi: 10.2217/cns-2020-0006. Epub 2020 Jun 30.
Atypical teratoid/rhabdoid tumor (ATRT) is a malignant CNS embryonal tumor that mostly occurs in childhood, adult cases are rare. We report a case of a 23-year-old male with an extra-axial dura-based lesion in the left frontal area, previously diagnosed as gliosarcoma. After 6 years, the patient had a recurrence and the previous slides were reviewed. Tumor was positive for vimentin and negative for INI1. The differential diagnosis for this extra-axial tumor with long survival was rhabdoid meningioma with INI1 loss or ATRT. DNA methylation profiling was performed to reach the final and the most definitive diagnosis; the result was ATRT. Our case suggests the usefulness of DNA methylation profiling for diagnosing challenging CNS tumors.
非典型畸胎样/横纹肌样瘤(ATRT)是一种主要发生在儿童期的恶性中枢神经系统胚胎瘤,成人病例罕见。我们报告了一例 23 岁男性患者,其左额区存在颅外硬脑膜基病变,此前诊断为胶质肉瘤。6 年后,患者复发,重新审查了之前的切片。肿瘤阳性表达波形蛋白,阴性表达 INI1。对于这种具有长生存期的颅外肿瘤,鉴别诊断包括 INI1 缺失的横纹肌样脑膜瘤或 ATRT。进行 DNA 甲基化分析以做出最终和最明确的诊断;结果为 ATRT。我们的病例表明 DNA 甲基化分析在诊断具有挑战性的中枢神经系统肿瘤方面的有用性。