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Gliosarcoma with Primary Skull Base Invasion

机译:胶质肉瘤伴原发性颅底侵犯

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摘要

Gliosarcoma is an uncommon variant of glioblastoma, which commonly demonstrates dural attachment. However, skull base invasion is rarely seen with this entity. Herein, we report a 44-year-old female patient diagnosed with primary intracranial gliosarcoma extensively invading the skull base and muscles of mastication. She presented to our institution with a three-month history of difficult right jaw opening and retro-orbital pressure and one week of severe right-sided postauricular headache. Head CT demonstrated a 6 cm mass with marked bony erosion. Brain MRI at a one-week interval more clearly characterized tumor extension through the right orbit and muscles of mastication, with overall growth to 7 cm and worsening midline shift. The patient underwent a right frontotemporal craniotomy for gross total resection. Pathology confirmed the diagnosis of gliosarcoma, IDH-wildtype (WHO grade IV). Her postoperative course was uneventful and she was discharged at preoperative neurologic baseline. To our knowledge, this is the third reported case of a primary intracranial gliosarcoma with direct invasion of skull base, brain parenchyma, and extracranial compartment. However, this is the first report case of primary GS invading the surrounding musculature and orbit. This case report highlights the rapid aggressiveness of gliosarcomas and further a prior undescribed radiographic and anatomic finding of skull base invasion with this entity.
机译:胶质肉瘤是胶质母细胞瘤的罕见变体,通常表现出硬脑膜附着。但是,此实体很少见到颅底侵犯。本文中,我们报道了一名44岁的女性患者,其诊断为原发性颅内神经胶质肉瘤,广泛侵犯颅底和咀嚼肌。她向我们的机构介绍了三个月的困难颌骨张开和眼眶后压的病史以及一个星期的严重右耳后头痛的病史。头颅CT表现为6 cm的肿块,明显骨侵蚀。每隔一周进行一次脑部MRI检查,可以更清楚地表征肿瘤通过右眼眶和咀嚼肌的延伸,整体增长到7 cm,中线移位恶化。该患者进行了右额颞开颅手术,以进行全切除。病理证实诊断为神经胶质肉瘤,IDH野生型(WHO IV级)。术后病情平稳,术前神经系统基线出院。据我们所知,这是第三例报道的原发性颅内神经胶质肉瘤,直接侵犯颅底,脑实质和颅外腔。但是,这是主要GS入侵周围肌肉和轨道的第一例报道。该病例报告强调了胶质肉瘤的快速侵袭性,并进一步揭示了该实体先前未描述的颅底侵犯的影像学和解剖学发现。

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