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A rare case of gliomatosis cerebri lurking beneath the shadows of a stroke mimic

机译:一种罕见的胶石症患者潜伏在中风的阴影下方

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摘要

Gliomatosis cerebri (GC) is a diffuse infiltrative neoplastic glial process with a devastating prognosis. Considering its rarity, unpredictable clinical manifestations, and lack of characteristic radiographic features, GC is a difficult diagnosis that is quite often delayed. In this report, we present a case of a 61-year-old man with a history of chronic alcohol abuse and atrial fibrillation who presented with right arm weakness initially presumed to be from an acute ischemic stroke. GC was not diagnosed until six months after initial symptoms and diagnosis was indicated when considering the neurocognitive findings in conjunction with suggestive radiographic findings. The presence of a rapid, expansile lesion in the cortex, corpus callosum, and infratentorial structures with mild parenchymal enlargement, as shown in our case, is more revealing of an invasive entity typical of GC rather than an ischemic process and other pathologies. This case demonstrates the fatal challenges of its prompt recognition and the therapeutic limitations for those patients presenting with advanced symptoms at the time of diagnosis. Recognizing GC in cases with such rapid multilobe clinical features with similar diffusely invasive patterns of growth on imaging can avoid a delay in diagnosis and improve patient quality of life.
机译:细胞病变脑病(GC)是具有毁灭性预后的弥漫性渗透肿瘤胶质过程。考虑到其罕见,不可预测的临床表现,缺乏特征射线照相特征,GC是一个难以延迟的难度诊断。在本报告中,我们提出了一个61岁的男子,历史历史历史悠久的慢性酒精滥用和心房颤动,右侧的弱臂呈现出急性缺血性卒中。在初始症状和诊断后六个月没有被诊断出来,在暗示与暗示放射线摄影结果结合时达到初始症状和诊断。如我们案例所示,在皮质,语料愈伤组织胼um和Infratential结构中存在快速,可膨胀的病变,具有轻微的实质扩大,更透露GC的典型侵入实体,而不是缺血过程和其他病理学。本例证明了其迅速识别的致命挑战以及在诊断时患有先进症状的患者的治疗限制。识别出具有如此快速多机临床特征的GC,具有相似的成像性增长的较为狡猾的侵入性模式,可以避免延迟诊断和改善患者的生活质量。

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