Furukawa Takahiro, Matsui Naoko, Tanaka Keiko, Izumi Yuishin, Kaji Ryuji
Department of Neurology, Institute of Biomedical Sciences, Tokushima University Graduate School.
Rinsho Shinkeigaku. 2017 Feb 25;57(2):77-81. doi: 10.5692/clinicalneurol.cn-000924. Epub 2017 Jan 28.
A 33 year-old woman presented with intentional incontinence, motor aphasia, supranuclear gaze palsy, and spasticity after parotitis. Brain magnetic resonance images (MRI) showed abnormal signaling in long corticospinal tract involving internal capsules and cerebral peduncles, middle cerebellar peduncle, and frontal subcortical white matter lesions. She had a long history of dry eye and mouth. Immunoserological study showed that she was positive for anti-SS-A, aquaporin 4 (AQP4), and AQP5 antibodies. She clinically showed not only Sjögren's syndrome but also neuromyelitis optica spectrum disorder (NMOSD) without optic neuritis or myelitis. She responded to steroid followed by plasma exchange dramatically. Thereafter, the relapse of brain lesion was once detected while tapering of steroid, but her symptoms have been stable for several years after administration of immunosuppressant. This case suggested that salivary gland inflammation might be associated with the pathogenesis of NMOSD.
一名33岁女性在腮腺炎后出现故意性尿失禁、运动性失语、核上性凝视麻痹和痉挛。脑磁共振成像(MRI)显示长皮质脊髓束信号异常,累及内囊和大脑脚、小脑中脚以及额叶皮质下白质病变。她有长期的干眼和口干病史。免疫血清学研究表明,她抗SS - A、水通道蛋白4(AQP4)和水通道蛋白5抗体呈阳性。她临床上不仅表现为干燥综合征,还表现为视神经脊髓炎谱系障碍(NMOSD),但无视神经炎或脊髓炎。她对类固醇治疗随后进行血浆置换反应显著。此后,在逐渐减少类固醇剂量时曾检测到脑病变复发,但在给予免疫抑制剂后她的症状已稳定数年。该病例提示唾液腺炎症可能与NMOSD的发病机制有关。