Uribe S M Reinaldo, Suárez H Felipe, Sandoval R Patricio, Mellado T Patricio
Rev Med Chil. 2013 Sep;141(9):1211-5. doi: 10.4067/S0034-98872013000900016.
Anti-GQ1b syndrome includes Miller Fisher Syndrome (MFS), Guillain Barré Syndrome (GBS), Bicker staff`s brain stem encephalitis (BBE) and Acute Ophtamoplegia (AO). We report four patients aged 16 to 76 years, with anti-GQ1b syndrome. All presented with MFS, one of them evolved to GBS pharyngeal-cervical-brachial variant and other to GBS with BBE. All had a previous history of diarrhea or upper respiratory tract infection. All had positive anti-GQ1b serum antibodies. Both brain magnetic resonance imaging and cerebrospinal fluid analysis were normal. Electrophysiology studies were compatible with a demyelinating disease. Two patients needed airway protection with an orotracheal tube and developed dysautonomia. All four patients were treated with immunomodulation. On the sixth month follow-up, patients had only minimal alterations in the neurological examination.
抗GQ1b综合征包括米勒费雪综合征(MFS)、吉兰-巴雷综合征(GBS)、比克斯特法夫脑干脑炎(BBE)和急性眼肌麻痹(AO)。我们报告了4例年龄在16至76岁之间的抗GQ1b综合征患者。所有患者均表现为MFS,其中1例演变为GBS咽颈臂型,另1例演变为合并BBE的GBS。所有患者既往均有腹泻或上呼吸道感染史。所有患者抗GQ1b血清抗体均为阳性。脑磁共振成像和脑脊液分析均正常。电生理研究结果与脱髓鞘疾病相符。2例患者需要经口气管插管进行气道保护,并出现了自主神经功能障碍。所有4例患者均接受了免疫调节治疗。在随访的第6个月,患者神经系统检查仅有轻微改变。