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一名原发性家族性脑钙化患者合并脑膜瘤:病例报告。

Coexistent meningioma in a patient with primary familial brain calcification: A case report.

作者信息

Scalia Gianluca, Costanzo Roberta, Marrone Salvatore, Iacopino Domenico Gerardo, Galvano Gianluca, Nicoletti Giovanni Federico, Umana Giuseppe Emmanuele

机构信息

Department of Head and Neck Surgery, Neurosurgery Unit, Garibaldi Hospital, Piazza Santa Maria di Gesù, 5, Catania, 95123 Italy.

Experimental Biomedicine and Clinical Neurosciences, School of Medicine, Postgraduate Residency Program in Neurological Surgery, Neurosurgical Clinic, AOUP "Paolo Giaccone", Via del Vespro 129, Palermo, 90127 Italy.

出版信息

Radiol Case Rep. 2023 Mar 5;18(5):1838-1843. doi: 10.1016/j.radcr.2023.02.004. eCollection 2023 May.

Abstract

Primary familial brain calcification (PFBC) is an idiopathic pathology characterized by the development of calcific deposits in the supratentorial region such as telencephalon and diencephalon but also, in more extensive forms, in the cerebellum. Meningiomas are among the most common central nervous system (CNS) tumors generally related to a good prognosis. The simultaneous presence of intracerebral or extra-axial tumors and PFBC represents an exceedingly rare occurrence. A 72-year-old female patient was admitted to our department because of anoculogyric crisis followed by generalized seizures. She performed a brain CT scan which showed widespread hyperdensities in the paraventricular supratentorial region, basal ganglia and at the level of bilateral cerebellar dentate nuclei, characteristics of PFBC. Concomitant left frontal and smaller right temporal extra-axial lesions were identified and then confirmed in a brain MRI. The patient underwent a microsurgical resection of the lesion and subsequent histological examination reported a meningothelial meningioma (WHO Grade I). According to our literature review, this is the first paper that reports the coexistence of both intracranial meningiomas and PFBC. To date, it is not possible to provide an exact correlation between pathogenesis and genetic mechanism underlying this association.

摘要

原发性家族性脑钙化(PFBC)是一种特发性病理状态,其特征是在幕上区域如端脑和间脑出现钙化沉积,更广泛的形式还包括小脑。脑膜瘤是最常见的中枢神经系统(CNS)肿瘤之一,通常预后良好。脑内或轴外肿瘤与PFBC同时存在极为罕见。一名72岁女性患者因动眼危象继而全身性癫痫发作入院。她进行了脑部CT扫描,显示脑室旁白质幕上区域、基底神经节以及双侧小脑齿状核水平广泛高密度影,这是PFBC的特征。同时发现左额叶和较小的右侧颞叶轴外病变,随后脑部MRI证实了这一发现。患者接受了病变的显微手术切除,随后的组织学检查报告为脑膜内皮型脑膜瘤(WHO一级)。根据我们的文献综述,本文是首次报道颅内脑膜瘤与PFBC共存的文章。迄今为止,尚无法确切说明这种关联背后的发病机制与遗传机制之间的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e889/10009674/dd0f8b1c03dd/gr1.jpg

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