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水通道蛋白4阳性视神经脊髓炎谱系障碍连续复发中的镜像病变

Mirror-Image Lesions in Sequential Relapses of AQP4-Positive Neuromyelitis Optica Spectrum Disorder.

作者信息

Muir Ryan T, Bharatha Aditya, Rotstein Dalia

机构信息

Division of Neurology, Department of Medicine, University of Toronto, Toronto, ON, Canada.

Division of Neuroradiology, Department of Radiology, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada.

出版信息

Front Neurol. 2020 May 12;11:414. doi: 10.3389/fneur.2020.00414. eCollection 2020.

Abstract

A 25 year-old Nigerian woman with aquaporin-4 antibody-positive neuromyelitis optica spectrum disorder (NMOSD) presented with a 6 week history of nausea, vomiting, and refractory hiccups; as well as progressive lower extremity sensory loss, weakness, saddle anesthesia, and urinary incontinence. She had experienced her first NMOSD relapse seven years prior with bilateral lower extremity weakness and area postrema syndrome. After pulse steroids and plasma exchange she made a complete neurologic recovery and was started on azathioprine. An initial aquaporin-4 (AQP4) antibody ELISA test was positive, but three subsequent tests were negative and repeat MRI brain showed resolution of T2/FLAIR signal abnormalities with the exception of a right thalamic lesion and a left medullary lesion. Azathioprine was discontinued after 1 year and she was lost to follow-up. With her second relapse, she had new lesions in her left thalamus and right medulla-a mirror image of the thalamic and medullary lesions associated with her first relapse. In addition, an MRI spine demonstrated a new longitudinally extensive transverse myelitis from T7 to L1 with edematous expansion of the cord. Her serum AQP4 antibody test using a cell-based assay was strongly positive. NMOSD lesions are typically associated with brain regions with high density of the AQP4 channel. These areas include optic nerves, hypothalamus, and the diencephalic and brainstem tissues that surround the cerebral aqueduct and third and fourth ventricles. Previous studies have demonstrated that those with relapsing NMOSD have a predilection for recurrence in the same neuroanatomical region as their first episode. We hypothesize, using data from prior pathologic and epidemiologic studies, that mirror image lesions, where the same anatomic sites are affected on the contralateral side of the brain or spinal cord, may appear in subsequent attacks due to (i) areas of high remaining AQP4 density and/or (ii) local compromise of astrocyte or blood-brain barrier (BBB) function that persists after the initial inciting attack.

摘要

一名25岁的尼日利亚女性,患有水通道蛋白4抗体阳性的视神经脊髓炎谱系障碍(NMOSD),出现了6周的恶心、呕吐和难治性呃逆病史;以及进行性下肢感觉丧失、无力、鞍区麻醉和尿失禁。她在7年前首次出现NMOSD复发,表现为双侧下肢无力和最后区综合征。经过脉冲类固醇和血浆置换治疗后,她的神经系统完全恢复,并开始服用硫唑嘌呤。最初的水通道蛋白4(AQP4)抗体ELISA检测呈阳性,但随后的三次检测均为阴性,重复脑部MRI显示T2/FLAIR信号异常消失,仅右侧丘脑和左侧延髓有病变。硫唑嘌呤在服用1年后停药,她随后失访。第二次复发时,她左侧丘脑和右侧延髓出现了新病变——与首次复发时的丘脑和延髓病变呈镜像。此外,脊柱MRI显示从T7到L1出现了新的纵向广泛横贯性脊髓炎,脊髓水肿扩大。她使用基于细胞的检测方法进行的血清AQP4抗体检测呈强阳性。NMOSD病变通常与水通道蛋白4通道高密度的脑区相关。这些区域包括视神经、下丘脑以及围绕中脑导水管和第三、第四脑室的间脑和脑干组织。先前的研究表明,复发型NMOSD患者在与其首次发作相同的神经解剖区域有复发倾向。我们根据先前的病理学和流行病学研究数据推测,镜像病变(即大脑或脊髓对侧相同解剖部位受到影响)可能会在后续发作中出现,原因可能是:(i)剩余AQP4密度高的区域和/或(ii)初始激发发作后持续存在的星形胶质细胞或血脑屏障(BBB)功能局部受损。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8350/7235314/7474a2ec127a/fneur-11-00414-g0001.jpg

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