Sohail Hafsah Binte, Ahmed Noman, Shamim Muhammad Shahzad, Mushtaq Naureen
Aga Khan University Hospital, National Stadium Rd, Karachi, Karachi City, Sindh, Pakistan.
Section of Neurosurgery, Department of Surgery, Aga Khan University Hospital, Karachi City, Sindh, Pakistan, Karachi.
Childs Nerv Syst. 2025 Mar 26;41(1):141. doi: 10.1007/s00381-025-06803-7.
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.
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.
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.
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.
幕上室管膜瘤是罕见肿瘤,在成人中尤为如此,在影像学上其表现可能与更常见的轴外肿块(如脑膜瘤)相似。区分这些病变对于恰当的治疗管理至关重要。
一名16岁女孩有1.5年的头痛病史,偶尔视力模糊,近期有癫痫发作。磁共振成像(MRI)显示左顶颞区有一个4.7×4.0×6.9厘米、基于硬脑膜的轴外病变,最初推测为脑膜瘤。患者接受了神经导航引导下的开颅手术切除病变。术中所见为一个质地柔软、血管丰富的实性囊性轴外肿块,基于术前影像学最初诊断为脑膜瘤,但后来通过组织病理学和分子分析确诊为幕上室管膜瘤,ZFTA融合阳性,世界卫生组织(WHO)中枢神经系统3级。术后,患者无神经功能缺损,随访影像学检查发现有残留肿瘤。
本病例说明了幕上轴外室管膜瘤表现类似脑膜瘤这种罕见情况所带来的诊断挑战。虽然脑膜瘤是最常见的轴外颅内肿瘤,但一些影像学特征,如囊性表现和多房性,应引起对室管膜瘤或其他类似病变的怀疑。然而,只有通过组织病理学检查才能做出明确诊断。
幕上轴外肿块常被误诊为脑膜瘤。此类室管膜瘤在影像学上可与脑膜瘤极为相似。本病例强调了对轴外肿块保持广泛鉴别诊断的重要性,并突出了某些影像学特征在帮助准确诊断或至少引起对脑膜瘤类似病变怀疑方面的作用。