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替莫唑胺同步放疗治疗进展性单纯胚胎发育不良性神经上皮肿瘤的放射学反应

Radiologic response to radiation therapy concurrent with temozolomide for progressive simple dysembryoplastic neuroepithelial tumor.

作者信息

Morr Simon, Qiu Jingxin, Prasad Dheerendra, Mechtler Laszlo L, Fenstermaker Robert A

机构信息

Department of Neurosurgery, School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, Albany, NY, USA.

Department of Pathology, Roswell Park Cancer Institute, Buffalo, New York, USA.

出版信息

Acta Neurochir (Wien). 2016 Jul;158(7):1363-6. doi: 10.1007/s00701-016-2832-2. Epub 2016 May 16.

Abstract

Dysembryoplastic neuroepithelial tumors (DNETs) are low-grade neuroglial tumors that are traditionally considered to be benign hamartoma-like mass lesions. Malignant transformation and disease progression have been reported in complex DNETs. We report a case of a simple DNET with disease progression following subtotal resection. A 34-year-old woman underwent craniotomy with subtotal resection of a large nonenhancing right temporal lobe and insular mass. Histopathological analysis revealed a simple DNET. Magnetic resonance imaging obtained 6 months after surgery demonstrated disease progression with no enhancement or change in signal characteristics. Following concurrent therapy with temozolomide and external beam radiation therapy, a significant radiologic response was observed. Progressive DNET with malignant transformation exhibits predominantly glial transformation and occurs predominantly in complex DNETs. The histological classification of DNETs into simple, complex, and nonspecific are reviewed. Contrast-enhancing regions are more frequently seen in complex tumors, with nonenhancing regions having fewer complex histologic features. Close clinical and radiographic follow-up is important in all cases of DNET. Following tumor progression, radiation therapy with concurrent and adjuvant temozolomide chemotherapy may be an effective treatment.

摘要

胚胎发育不良性神经上皮肿瘤(DNETs)是一种低级别神经胶质瘤,传统上被认为是良性错构瘤样肿块病变。复杂型DNETs已有恶性转化和疾病进展的报道。我们报告一例单纯型DNETs在次全切除术后疾病进展的病例。一名34岁女性接受了开颅手术,次全切除了右侧颞叶和岛叶的一个大的无强化肿块。组织病理学分析显示为单纯型DNETs。术后6个月的磁共振成像显示疾病进展,无强化且信号特征无变化。在替莫唑胺和外照射放疗同步治疗后,观察到显著的放射学反应。伴有恶性转化的进行性DNETs主要表现为胶质细胞转化,且主要发生在复杂型DNETs中。对DNETs分为单纯型、复杂型和非特异性型的组织学分类进行了综述。强化区域在复杂肿瘤中更常见,无强化区域具有较少的复杂组织学特征。所有DNETs病例都进行密切的临床和影像学随访很重要。肿瘤进展后,同步和辅助替莫唑胺化疗的放射治疗可能是一种有效的治疗方法。

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