Department of Neurology, Dong-A University College of Medicine, Busan, Republic of Korea.
Department of Peripheral Neuropathy Research Center, Dong-A University College of Medicine, Busan, Republic of Korea.
Muscle Nerve. 2021 Mar;63(3):336-343. doi: 10.1002/mus.27126. Epub 2020 Dec 22.
We propose the finger drop sign as a new clinical variant of acute motor axonal neuropathy (AMAN) defined by immunological and radiological evidence. We identified eight consecutive patients who had AMAN. All of them developed prominent involvement of the finger extensors. We performed magnetic resonance imaging (MRI) of the extremity muscles and serological assays for antiganglioside antibodies and Campylobacter jejuni. Patients with AMAN showed characteristic and a markedly sustained weakness of the finger extensors with a distinctive pattern of the finger drop sign. Limb MRI revealed unevenly distributed abnormal signals in the muscles mainly innervated by the posterior interosseous nerve. All tested patients showed positivity for immunoglobulin G antibody against ganglioside complex of GM1 and phosphatidic acid. A pathophysiological understanding of this unique syndrome can provide further insight into antiganglioside-antibody-mediated axonal injury in Guillain-Barré syndrome.
我们提出手指下垂征作为急性运动轴索性神经病 (AMAN) 的一种新的临床变异型,其定义为免疫和影像学证据。我们确定了 8 例连续的 AMAN 患者。他们都出现了明显的手指伸肌受累。我们对四肢肌肉进行了磁共振成像 (MRI) 和血清学检测抗神经节苷脂抗体和空肠弯曲菌。AMAN 患者表现为特征性的、显著持续的手指伸肌无力,并伴有明显的手指下垂征模式。肢体 MRI 显示主要由骨间后神经支配的肌肉中分布不均匀的异常信号。所有检测到的患者对 GM1 和磷脂酸神经节苷脂复合物的 IgG 抗体呈阳性。对这种独特综合征的病理生理学理解可以进一步深入了解吉兰-巴雷综合征中抗神经节苷脂抗体介导的轴索性损伤。