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Cerebral infarct mimicking glioma in Sjogren's syndrome

机译:干燥综合征中模拟脑胶质瘤的脑梗塞

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A 50-year-old Chinese woman with a chronic 20-year history of ataxic gait associated with dry eyes and mouth, was admitted to hospital after a single episode of syncope. Magnetic resonance imaging scans showed a large left frontal hypodense lesion suggestive of a glioma. Craniotomy was performed and the lesion excised, with histology showing only infarcted tissue and no malignant cells. Further diagnostic evaluation revealed that the patient had primary Sjogren’s syndrome, with demyelinating polyneuropathy. In the absence of risk factors for stroke, it was considered likely that the cerebral infarct was secondary to autoimmune-related vasculitis. Functional neuroimaging, such as magnetic resonance spectroscopy, should be considered in evaluating doubtful or unusual brain lesions in patients with autoimmune disease.
机译:一名50岁的中国妇女,患有慢性20年的共济失调步态,伴有干眼和口干,单发晕厥发作后入院。磁共振成像扫描显示左额叶低密度大病变提示神经胶质瘤。进行颅骨切开术并切除病变,组织学仅显示梗死的组织,无恶性细胞。进一步的诊断评估表明,该患者患有原发性干燥综合征,伴有脱髓鞘性多发性神经病。在没有中风危险因素的情况下,认为脑梗死可能是继发于自身免疫相关血管炎的继发性疾病。在评估自身免疫性疾病患者的可疑或异常脑损伤时,应考虑使用磁共振成像等功能性神经影像学检查。

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