| Literature DB >> 33217007 |
Byeol-A Yoon1,2, Dong-Ho Ha3, Hwan Tae Park2,4, Susumu Kusunoki5, Motoi Kuwahara5, Jong Hwa Lee6, Jong Seok Bae7, Jong Kuk Kim1,2.
Abstract
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.Entities:
Keywords: Guillain-Barré syndrome; acute motor axonal neuropathy; antiganglioside antibodies; magnetic resonance imaging; posterior interosseous nerve
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Year: 2020 PMID: 33217007 DOI: 10.1002/mus.27126
Source DB: PubMed Journal: Muscle Nerve ISSN: 0148-639X Impact factor: 3.217