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首页> 外文期刊>Internal medicine. >A Case of Gliomatosis Cerebri Mimicking Limbic Encephalitis: Malignant Transformation to Glioblastoma
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A Case of Gliomatosis Cerebri Mimicking Limbic Encephalitis: Malignant Transformation to Glioblastoma

机译:一例胶质瘤样脑炎的脑胶质瘤病脑:恶性转化为胶质母细胞瘤。

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Gliomatosis cerebri (GC) is a specific entity defined as diffuse infiltration of neoplastic glial cells into at least three cerebral lobes and preservation of the surrounding neuronal architecture. We report a patient with secondary GC that mimicked clinicoradiological features of limbic encephalitis (LE). A 72-year-old man had developed headache and disorientation insidiously 2 weeks previously. On admission, neurological examination showed confusion and hyperreflexia in the right extremities. Brain magnetic resonance imaging (MRI) revealed T2-hyperintensity in bilateral frontal, the left parietal, the left temporal lobes and bilateral posterior periventricular zones. Slight enhancement existed in the left lower temporal region. Cerebral angiography exhibited no tumor stains. Repeated cerebrospinal fluid studies showed mild pleocytosis and cytology of class I. There were no infectious pathogenic agents. His neurological symptoms were ameliorated at 7 days after treatment with dexamethasone and glycerol. Follow-up MRI showed no pathognomonic changes. Mild memory dysfunction remained. He was diagnosed as LE of unknown cause. Three months later he became disorientated. Brain CT revealed a hemorrhagic mass with surrounding edema in the left temporal, frontal and parietal lobes. MRI displayed marked enhancement in these regions. Urgent neurosurgery was performed and glioblastoma multiforme (GM) was confirmed pathologically. The early clinicoradiological course of this patient suggested similarities to LE. At 3 months after clinical onset, the neuroradiological features reflected rapid transformation from secondary GC to massive GM. Thus, it is important to pay more attention to the differential diagnoses of GC and LE in patients who have memory deficits and widespread MRI lesions.
机译:脑胶质瘤(GC)是一个特定实体,定义为赘生性神经胶质细胞向至少三个脑叶中扩散浸润并保留周围神经元结构。我们报告了一名继发性GC患者,该患者模仿了边缘性脑炎(LE)的临床放射学特征。一名72岁的男子在2周前隐匿了头痛和迷失方向。入院时,神经系统检查显示右肢混乱和反射亢进。脑磁共振成像(MRI)显示双侧额叶,左顶叶,左颞叶和双侧后脑室周围区域的T2高强度。左下颞区存在轻微增强。脑血管造影未显示肿瘤斑。反复的脑脊液研究显示轻度的胞浆增多症和I类细胞学检查。没有传染性病原体。地塞米松和甘油治疗后7天,他的神经症状得到改善。随访MRI未显示病原学改变。轻度记忆功能障碍仍然存在。他被诊断为原因不明的LE。三个月后,他迷失了方向。脑部CT显示左侧颞叶,额叶和顶叶有出血性肿块,周围有水肿。 MRI在这些区域显示出明显的增强。进行了紧急神经外科手术,并在病理上证实了多形性胶质母细胞瘤(GM)。该患者的早期临床放射学过程表明与LE相似。临床发作后3个月,神经放射学特征反映了从继发性GC快速转变为大量GM。因此,重要的是要更加注意患有记忆缺陷和广泛MRI病变的患者的GC和LE的鉴别诊断。

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