一位年轻女性的高级别星形母细胞瘤:一个具有罕见警示故事的谜

IF 0.3 Q4 SURGERY
Mukta Meel, A. Gandhi, A. Jindal, Mukesh Kumar
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引用次数: 0

摘要

星形母细胞瘤是一种罕见的神经上皮性原发性脑肿瘤,其组织病理学起源不明,临床行为难以预测。它们很容易被误诊,因为它们在临床实践中很少遇到,并且与其他神经胶质肿瘤具有共同的放射学和组织病理学表现。在此,我们报告一位27岁的女性患者,以癫痫发作和意识丧失为主诉,在神经影像学上被误诊为非典型脑膜瘤,因为它的罕见性和浅表皮质位置表现为轴外肿块。虽然术中发现也为轴外肿瘤,但组织学和免疫表型为星形母细胞瘤;因此,强调组织病理学和免疫组织化学的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-Grade Astroblastoma in a Young Female: An Enigma with a Rare Cautionary Tale
Abstract Astroblastoma is an uncommon neuroepithelial primary brain neoplasm with speculative histopathological origin and unpredictable clinical behavior. They can be easily misdiagnosed, as they are rarely encountered in clinical practice and share common radiological and histopathologic appearances with other glial neoplasms. Herein, we report a case of high-grade astroblastoma in a 27-year-old female with complaints of seizures and loss of consciousness, which was misdiagnosed as atypical meningioma on neuroimaging, due to its rarity and superficial cortical location appearing as extra-axial mass. Although intraoperative findings were also of an extra-axial tumor, the histology and immunophenotype was of an astroblastoma; thus, highlighting the role of histopathology and immunohistochemistry.
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来源期刊
CiteScore
0.40
自引率
0.00%
发文量
52
审稿时长
12 weeks
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