De Novo Glioblastoma Masqueraded within a Hemispheric Dural Meningiomatosis: Rare Imaging Findings and Rationale for Two-Staged Resection

IF 0.6 Q4 CLINICAL NEUROLOGY
Nicholas Zacharewski, Misha Movahed-Ezazi, Xianyuan Song, T. Mehta, S. Manjila
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引用次数: 2

Abstract

Introduction  Collision tumors present as histologically different juxtaposed neoplasms within the same anatomical region, independent of the adjacent cell population. De novo intracranial collision tumors involving metachronous primary brain neoplasms alongside dural meningiomatosis are not well documented in the literature. Clinical Presentation  We present staged surgical management of a 72-year-old female with known left hemispheric stable dural-based convexity mass lesions over 10 years and new-onset expressive aphasia and headaches. MRI had revealed left supratentorial dural-based enhanced masses consistent with en plaque meningiomatosis. Embolization angiography showed an unusual tumor blush from an aberrant branch of anterior cerebral artery suggesting a deeper focal intra-axial nature; a stage 1 craniotomy for dural-based tumor resection was completed with diagnosis of a meningioma (WHO grade 1). Intraoperatively, a distinct intra-axial deep discrete lesion was verified stereotactically, concordant with the location of tumor blush. The patient made a complete neurological recovery from a transient postoperative supplemental motor area syndrome in a week. Subsequent postoperative follow-up showed worsening of right hemiparesis and MRI showed an increase in residual lesion size and perilesional edema, which prompted a stage 2 radical resection of a glioblastoma, WHO grade 4. She improved neurologically after surgery with steroids and physical therapy. At 15 months following adjuvant therapy, she remains neurologically intact throughout the postoperative course, with no recurrent tumor on MRI. Conclusion  A de novo glioblastoma presented as a masquerading lesion within hemispheric convexity meningiomatosis in an elderly patient with no prior radiation/phakomatosis, inciting a non-causal juxtapositional coexistence. The authors highlight rare pathognomonic angiographic findings and the rationale for two-staged resections of these collision lesions that led to excellent clinicoradiological outcome.
新发胶质母细胞瘤伪装在半球硬脑膜瘤:罕见的影像学发现和两期切除的理由
碰撞肿瘤在同一解剖区域内表现为组织学上不同的并置肿瘤,独立于相邻细胞群。新发颅内碰撞瘤伴发异时性原发性脑肿瘤伴发硬脑膜脑膜瘤的文献报道并不多见。临床表现:我们报告一名72岁女性患者的分阶段手术治疗,她已知的左半球稳定硬脑膜凸性肿块病变超过10年,并新发表达性失语和头痛。MRI显示左侧幕上硬脑膜增强肿块与斑状脑膜瘤一致。栓塞血管造影显示大脑前动脉异常分支的异常肿瘤红,提示更深的局灶轴内性质;诊断为脑膜瘤(WHO分级为1级),完成了一期硬脑膜肿瘤切除术。术中,立体定向证实了明显的轴内深部离散病变,与肿瘤腮红的位置一致。患者术后短暂性辅助运动区综合征在一周内神经系统完全恢复。随后的术后随访显示右半瘫恶化,MRI显示残留病变大小和病灶周围水肿增加,这促使了2期胶质母细胞瘤根治性切除术,WHO 4级。手术后使用类固醇和物理治疗,神经系统得到改善。在辅助治疗后的15个月,患者的神经系统在整个术后过程中保持完整,MRI显示无复发肿瘤。结论:1例老年患者既往无放疗/瘤化,新发胶质母细胞瘤表现为半球凸性脑膜瘤内的伪装病变,引发非因果并列共存。作者强调了罕见的病理血管造影结果和两阶段切除这些碰撞病变的基本原理,这些碰撞病变导致了良好的临床放射学结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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