Barbagallo Gaetano, Caggiula Marcella, Lupo Angela, Rizzo Annalisa, My Filomena, Marulli Daniele, Barbarini Leonardo
Division of Neurology, Vito Fazzi Hospital, Lecce, Italy.
Division of Neurology, Vito Fazzi Hospital, Lecce, Italy.
Clin Neurol Neurosurg. 2021 Jul;206:106691. doi: 10.1016/j.clineuro.2021.106691. Epub 2021 May 17.
Miller-Fisher syndrome (MFS) together with Guillan-Barré syndrome (GBS) and Bickerstaff brainstem encephalitis (BBE) are considered to form a continuous clinical spectrum of the same disease, possibly affecting the peripheral and/or central nervous systems, with monophasic symptoms. The frequency of overlapping clinical signs and the risk of recurrence are independent and very low, but no cases of GQ1b-seropositive recurrent MFS overlapping with GBS and BBE have been described so far. Here, we describe for the first time an atypical case of recurrent GQ1b-seropositive MFS overlapping GBS and BBE, 12 years after a previous GQ1b-seronegative typical MFS episode. Our case expands the clinical spectrum of recurrent MFS, and it should prompt clinicians to investigate the presence of anti-ganglioside antibodies in recurrent MFS even when these were negative in the previous episode, especially in those presenting with overlapping spectrum symptoms and a critically ill picture during the second episode.
米勒-费希尔综合征(MFS)与吉兰-巴雷综合征(GBS)和比克斯特法夫脑干脑炎(BBE)被认为构成了同一种疾病的连续临床谱,可能影响周围和/或中枢神经系统,症状为单相性。重叠临床体征的发生率和复发风险相互独立且非常低,但迄今为止,尚未有GQ1b血清阳性复发性MFS与GBS和BBE重叠的病例报道。在此,我们首次描述了一例非典型复发性GQ1b血清阳性MFS病例,该病例在之前一次GQ1b血清阴性的典型MFS发作12年后,与GBS和BBE重叠。我们的病例扩展了复发性MFS的临床谱,并且应促使临床医生即使在之前发作时抗神经节苷脂抗体为阴性,尤其是在那些出现重叠谱症状且在第二次发作时病情危重的复发性MFS患者中,也应对抗神经节苷脂抗体的存在进行调查。