Dosi Rupal, Ambaliya Annirudh, Patel Niyati, Shah Monisha, Patell Rushad
Department of Medicine, Medical College, Baroda, Gujarat, India 376.
Australas Med J. 2014 Sep 30;7(9):376-8. doi: 10.4066/AMJ.2014.2123. eCollection 2014.
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.
我们报告了一例20岁男性患者,他以双侧完全性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变。患者血液学和生化检查正常,然而,脑脊液(CSF)分析显示在发病第二周蛋白质升高(96mg/dl)。周围神经传导研究和脑部MRI正常。经过三周的支持治疗,患者病情逐渐好转。考虑到病程以及临床和检查结果,诊断为格林-巴利综合征(GBS)的眼咽型变体。