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Acute Multiple Cranial Neuropathy-a cranial variant of Guillain Barre Syndrome

机译:急性多发性颅神经病-格林巴利综合征的一种颅脑变异

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We report the case of a 20-year-old male who presented to us with acute bilateral multiple cranial neuropathy in the form of bilateral total ophthalmoplegia and bulbar dysfunction. The patient had normal haematological and biochemical investigations, however, cerebrospinal fluid (CSF) analysis showed raised protein (96mg/dl) in the second week of illness. Peripheral nerve conduction studies and an MRI of the brain were normal. The patient showed gradual improvement after three weeks of supportive treatment. Considering the course of illness and the clinical and investigational profile, a diagnosis of an oculopharyngeal variant of Guillain-Barré syndrome (GBS) was made.
机译:我们报告了一个病例,该病例是一名20岁男性,以双侧全眼肌麻痹和延髓功能障碍的形式出现急性双侧多发性颅神经病。该患者的血液学和生化检查正常,但是脑脊液(CSF)分析显示,疾病第二周的蛋白质升高(96mg / dl)。周围神经传导研究和脑部MRI正常。在三周的支持治疗后,患者逐渐改善。考虑到病程以及临床和研究概况,对吉兰-巴雷综合征(GBS)的眼咽变异进行了诊断。

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