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一名伴有GQ1b抗体和水通道蛋白4抗体阳性的米勒-费希尔综合征患者:是否会出现与水通道蛋白4抗体相关的疾病?

A Patient With Miller Fisher Syndrome With Positive GQ1b and Aquaporin-4 Antibodies: Will There Be an Aquaporin-4 Antibody Associated Disorder?

作者信息

Aylia Fatin, Johri Karn, Spencer Riley, Chu David, Deriss Mehron, Peng Davin, Eskenazi Jonathan, Liu Antonio K

机构信息

Internal Medicine, Adventist Health White Memorial, Los Angeles, USA.

Family Medicine, Charleston Area Medical Center, Charleston, USA.

出版信息

Cureus. 2023 Aug 13;15(8):e43428. doi: 10.7759/cureus.43428. eCollection 2023 Aug.

Abstract

There have been many advancements in the field of neuromyelitis optica and neuromyelitis optica spectrum disorder since the discovery of aquaporin-4 (AQP4) and myelin oligodendrocyte glycoprotein antibodies. It is also recognized that the pathological features associated with myelin oligodendrocyte glycoprotein antibodies are beyond the domain of neuromyelitis optica spectrum disorder and there is a separate nomenclature, namely myelin oligodendrocyte glycoprotein antibody associated disease. Currently, there is no aquaporin-4 antibody associated disorder, even though aquaporin-4 antibodies are not as widely present in other disorders.  Miller Fisher syndrome (MFS) is a variant of Guillain Barré syndrome, in which there are positive GQ1b antibodies with no evidence of myelitis or optic neuritis. MFS is not considered a component of neuromyelitis optica spectrum disorder. We report on a patient with MFS that was positive for GQ1b and aquaporin-4 antibodies but negative for myelin oligodendrocyte glycoprotein antibodies and is devoid of any features of neuromyelitis optica spectrum disorder. This finding may lead to investigations and reports of other pathologies that are associated with the aquaporin-4 antibody.

摘要

自从发现水通道蛋白4(AQP4)和髓鞘少突胶质细胞糖蛋白抗体以来,视神经脊髓炎和视神经脊髓炎谱系障碍领域取得了许多进展。人们还认识到,与髓鞘少突胶质细胞糖蛋白抗体相关的病理特征超出了视神经脊髓炎谱系障碍的范畴,并且有一个单独的命名,即髓鞘少突胶质细胞糖蛋白抗体相关疾病。目前,不存在水通道蛋白4抗体相关疾病,尽管水通道蛋白4抗体在其他疾病中并不广泛存在。米勒-费希尔综合征(MFS)是吉兰-巴雷综合征的一种变体,其中存在GQ1b抗体阳性,且无脊髓炎或视神经炎的证据。MFS不被认为是视神经脊髓炎谱系障碍的一个组成部分。我们报告了一名MFS患者,该患者GQ1b和水通道蛋白4抗体呈阳性,但髓鞘少突胶质细胞糖蛋白抗体呈阴性,且没有任何视神经脊髓炎谱系障碍的特征。这一发现可能会引发对与水通道蛋白4抗体相关的其他病理学的研究和报告。

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