Meningiomas of the parieto-occipital convexity mimicking a hematoma: A case report in a third-world country.

Surgical neurology international Pub Date : 2024-10-04 eCollection Date: 2024-01-01 DOI:10.25259/SNI_410_2024
Fatou Sène, Ebrima Kalilu Manneh, Job Manneh, Fansu F N Jatta, Fatoumatta S Jallow, John Nute Jabang
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Abstract

Background: Meningiomas are benign, slow-growing tumors of the central nervous system (CNS) that arise from the arachnoid matter. It comprises one of the most common primary tumors of the CNS, occurring mostly in and after the fifth decade of life with a female gender predilection. Diagnosis is facilitated by imaging computed tomography (CT) or magnetic resonance imaging (MRI); however, atypical forms exist which augments the risk of missing the diagnosis. This is a case of a meningioma that mimics a hematoma on imaging, the diagnosis of which was only confirmed following histopathology.

Case description: A 36-year-old patient presented with a 9-month history of intermittent moderate-intensity headaches associated with photophobia, tinnitus, and dizziness. There was no previous history of trauma. There were no focal neurological deficits on examination. Both contrast-enhanced and noncontrast-enhanced brain CT scans showed features suggestive of an intraparenchymal hematoma. She had a control CT scan 2 months and 9 months later due to the persistence of symptoms despite remaining stationary, which revealed no changes in the lesion as seen in the previous CT scans. The patient did not benefit from an MRI scan due to the socioeconomic status of the country and the patient herself. A decision to operate was made, and the sample was sent for histopathology. Histopathology confirmed the lesion to be a psammomatous meningioma.

Conclusion: Although CT findings of meningiomas are quite often typical, it is important to note that atypical forms exist as well. Knowledge of the atypical forms, such as lesions that look like an intraparenchymal hemorrhage initially but remain unchanged over a period of time, would decrease the risk of missing the diagnosis in such instances.

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模仿血肿的顶枕凸脑膜瘤:一个第三世界国家的病例报告。
背景:脑膜瘤是中枢神经系统(CNS)的良性肿瘤,生长缓慢,起源于蛛网膜。脑膜瘤是中枢神经系统最常见的原发性肿瘤之一,多发于五六十岁以后,女性多发。计算机断层扫描(CT)或核磁共振成像(MRI)有助于诊断;然而,非典型肿瘤的存在增加了漏诊的风险。本病例是一个脑膜瘤病例,影像学表现与血肿相似,组织病理学检查后才确诊:一名 36 岁的患者有 9 个月的间歇性中等强度头痛病史,伴有畏光、耳鸣和头晕。既往无外伤史。检查无局灶性神经功能缺损。对比度增强型和非对比度增强型脑CT扫描均显示有胸膜内血肿的特征。2 个月后和 9 个月后,她分别进行了一次对照 CT 扫描,结果显示病变部位与之前的 CT 扫描结果相同。由于国家和患者本人的社会经济状况,患者无法从核磁共振扫描中获益。于是决定进行手术,并将样本送去进行组织病理学检查。组织病理学证实该病变为脓肿性脑膜瘤:尽管脑膜瘤的 CT 检查结果通常比较典型,但也要注意到非典型脑膜瘤的存在。了解非典型病变,如最初看起来像实质内出血,但一段时间后仍无变化的病变,可降低在这种情况下漏诊的风险。
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