多灶性硬脊膜内-髓外管端膜瘤合并颅内受累1例报告

K. Mozaffari, M. Stellon, E. Chalif, Michael K. Rosner
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引用次数: 0

摘要

背景和重要性:上皮细胞瘤是一种罕见的恶性肿瘤。多灶性硬膜外髓外间变性室管膜瘤是一种罕见的实体瘤,目前的大部分知识都来自病例报告。我们报告了一例多灶性髓外硬膜内间变性室管膜瘤,其表现为颅内受累。病例介绍:一名53岁男性,出现泌尿系统症状。磁共振成像显示两处沿脊髓的病变和两处颅内病变。组织病理学检查符合世界卫生组织III级间变性室管膜瘤。患者接受了脊髓病变的大体全切除治疗,然后对切除腔和颅内病变进行放射治疗。在10个月的随访中,他报告症状几乎完全缓解,磁共振成像显示没有复发。结论:尽管室管膜瘤罕见,但在评估脊柱肿瘤时应将其作为鉴别诊断。全切除加靶向放疗似乎是治疗高级别病变的有效方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multifocal Intradural Extramedullary Anaplastic Ependymoma With Intracranial Involvement at Presentation: A Case Report
Background and Importance: Ependymomas are a rare malignant neoplasm. Multifocal intradural extramedullary anaplastic ependymomas are even more of a rare entity with much of the current knowledge derived from case reports. We presented a case of a multifocal intradural extramedullary anaplastic ependymoma with intracranial involvement at presentation. Case Presentation: A 53-year-old male presented with urinary symptoms. Magnetic resonance imaging revealed two lesions along the spinal cord and two lesions, intracranially. Histopathological examination was consistent with the World Health Organization grade III anaplastic ependymoma. The patient was treated with the gross total resections of spinal cord lesions, followed by radiation therapy to the resection cavities and intracranial lesions. At the 10-month follow-up visit, he reported almost complete resolution of symptoms, and magnetic resonance imaging revealed no recurrence. Conclusion: Despite their rarity, ependymomas should be considered as the differential diagnosis when evaluating spinal tumors. Gross total resection followed by targeted radiotherapy appears to be an effective treatment modality for high-grade lesions.
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CiteScore
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