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首页> 外文期刊>Neuropathology: official journal of the Japanese Society of Neuropathology >Primary central nervous system angiosarcoma: A case report and literature review
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Primary central nervous system angiosarcoma: A case report and literature review

机译：原发性中枢神经系统血管肉瘤1例并文献复习

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摘要

Angiosarcoma is a rare vascular malignant neoplasm that mainly occurs in skin and soft tissues. Intracranial localization is very rare and only a few cases have been reported. This report intends to present the clinical, radiological and pathological pictures of a primary central nervous system angiosarcoma along with a review of the literature. A 35-year-old woman presented at our institution with weakness and sensory disturbances of her right hand. Neuroimaging revealed a roughly round, hemorrhagic and moderately enhancing lesion in the left frontal posterior region. The tumor was totally removed under awake anesthesia and continuous monitoring of motor and language functions. Histopathology revealed an epithelioid angiosarcoma. Radical removal, followed by adjuvant radiotherapy and chemotherapy, is able to completely control the disease for a relatively long period.
机译：血管肉瘤是一种罕见的血管恶性肿瘤，主要发生在皮肤和软组织中。颅内定位非常罕见，仅报道了少数病例。本报告旨在介绍原发性中枢神经系统血管肉瘤的临床，影像学和病理学图像，并对文献进行回顾。一名35岁的妇女在我们的机构中​​出现右手无力和感觉障碍。神经影像学检查显示左额叶后部区域有大致圆形，出血性和中度增强的病变。在清醒麻醉下并持续监测运动和语言功能，将肿瘤完全清除。组织病理学显示上皮样血管肉瘤。根治性切除，然后进行辅助放疗和化疗，能够在相对较长的时间内完全控制该疾病。

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