Beyond the expected: a supratentorial ependymoma imitating a meningioma.

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY
Hafsah Binte Sohail, Noman Ahmed, Muhammad Shahzad Shamim, Naureen Mushtaq
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引用次数: 0

Abstract

Introduction: Supratentorial ependymomas are rare tumors, particularly in adults, and can present similarly to more common extra-axial masses like meningiomas on imaging. Differentiating between these lesions is crucial for appropriate management.

Case presentation: A 16-year-old girl presented with a 1.5-year history of headaches, occasional blurring of vision, and a recent seizure. MRI revealed a 4.7 × 4.0 × 6.9 cm dural-based, extra-axial lesion in the left parietal-temporal region, initially presumed to be a meningioma. The patient underwent a neuronavigation-guided craniotomy with excision of the lesion. Intraoperative findings described a soft, vascular, solid-cystic extra-axial mass, which was initially diagnosed as a meningioma based on preoperative imaging but later confirmed to be a supratentorial ependymoma, ZFTA fusion-positive, CNS WHO grade 3, through histopathological and molecular analysis. Postoperatively, the patient showed no neurological deficits, and a residual tumor was identified on follow-up imaging.

Discussion: This case illustrates the diagnostic challenge posed by the rare presentation of supratentorial, extra-axial ependymomas mimicking meningiomas. Although meningiomas are the most common extra-axial intracranial tumors, some radiological features such as cystic appearance and multiloculation on imaging should raise suspicion for ependymoma or other mimics. However, a definitive diagnosis can only be made through histopathological examination.

Conclusion: Supratentorial, extra-axial masses are often misdiagnosed as meningiomas. Such ependymomas can closely resemble meningiomas on imaging. This case underscores the importance of maintaining a broad differential diagnosis for extra-axial masses and highlights the role of certain radiological features that can help with accurate diagnosis or at least raise suspicion of meningioma mimics.

出乎意料:类似脑膜瘤的幕上室管膜瘤。
幕上室管膜瘤是一种罕见的肿瘤,尤其在成人中,其影像学表现与更常见的轴外肿块如脑膜瘤相似。区分这些病变对于适当的治疗至关重要。病例介绍:一名16岁的女孩,有1.5年的头痛病史,偶尔视力模糊,最近癫痫发作。MRI示左侧顶叶颞区4.7 × 4.0 × 6.9 cm硬脑膜外病变,初步推测为脑膜瘤。患者接受了神经导航引导下切除病变的开颅手术。术中发现一软质、血管性、实性囊性轴外肿块,术前影像学初步诊断为脑膜瘤,后经组织病理学和分子分析证实为幕上室管膜瘤,ZFTA融合阳性,CNS WHO分级3级。术后,患者无神经功能缺损,随访影像学发现残留肿瘤。讨论:这个病例说明了罕见的幕上,轴外室管膜瘤模拟脑膜瘤的诊断挑战。虽然脑膜瘤是最常见的轴外颅内肿瘤,但一些影像学特征,如囊性外观和多房室分布,应引起室管膜瘤或其他类似肿瘤的怀疑。然而,一个明确的诊断只能通过组织病理学检查。结论:幕上、轴外肿块常被误诊为脑膜瘤。这种室管膜瘤在影像学上与脑膜瘤非常相似。本病例强调了对轴外肿块保持广泛鉴别诊断的重要性,并强调了某些放射学特征的作用,这些特征可以帮助准确诊断或至少引起对模拟脑膜瘤的怀疑。
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来源期刊
Child's Nervous System
Child's Nervous System 医学-临床神经学
CiteScore
3.00
自引率
7.10%
发文量
322
审稿时长
3 months
期刊介绍: The journal has been expanded to encompass all aspects of pediatric neurosciences concerning the developmental and acquired abnormalities of the nervous system and its coverings, functional disorders, epilepsy, spasticity, basic and clinical neuro-oncology, rehabilitation and trauma. Global pediatric neurosurgery is an additional field of interest that will be considered for publication in the journal.
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