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伴有原发性颅底侵犯的胶质肉瘤。

Gliosarcoma with Primary Skull Base Invasion.

作者信息

Nguyen Quoc-Bao D, Perry Avital, Graffeo Christopher S, Nesvick Cody L, Raghunathan Aditya, Jentoft Mark E, O'Neill Brian P, Morris Padraig P, Morris Jonathan M, Van Gompel Jamie J

机构信息

Texas A&M Health Science Center College of Medicine, Temple, TX, USA.

Department of Neurological Surgery, Mayo Clinic, Rochester, MN, USA.

出版信息

Case Rep Radiol. 2016;2016:1762195. doi: 10.1155/2016/1762195. Epub 2016 Dec 8.

Abstract

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.

摘要

胶质肉瘤是胶质母细胞瘤的一种罕见变体,通常表现为硬膜附着。然而,该实体很少见颅骨基底侵犯。在此,我们报告一名44岁女性患者,诊断为原发性颅内胶质肉瘤,广泛侵犯颅骨基底和咀嚼肌。她因右下颌开口困难和眶后压迫3个月以及严重的右侧耳后头痛1周前来我院就诊。头部CT显示一个6厘米的肿块,伴有明显的骨质侵蚀。间隔一周的脑部MRI更清楚地显示肿瘤延伸至右侧眼眶和咀嚼肌,总体生长至7厘米,中线移位加重。患者接受了右额颞开颅手术以进行全切除。病理证实为胶质肉瘤,异柠檬酸脱氢酶野生型(世界卫生组织IV级)。她的术后过程平稳,出院时神经功能恢复到术前基线水平。据我们所知,这是第三例报告的原发性颅内胶质肉瘤直接侵犯颅骨基底、脑实质和颅外间隙的病例。然而,这是首例原发性胶质肉瘤侵犯周围肌肉组织和眼眶的报告病例。本病例报告突出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骨基底侵犯的影像学和解剖学发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c016/5178354/081745387914/CRIRA2016-1762195.001.jpg

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