Zheng Wei, Liu Xiaoping, Hou Xiujuan, Zhu Yuelan, Zhang Taotao, Liao Liang
Beijing University of Chinese Medicine, Beijing.
Department of Endocrinology, The First Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, Zhejiang.
Medicine (Baltimore). 2020 Nov 6;99(45):e23029. doi: 10.1097/MD.0000000000023029.
Neuromyelitis optica spectrum disorder (NMOSD) patients, especially those with anti-aquaporin-4 antibody positivity, a water channel expressed on astrocytes, is often accompanied by autoimmune diseases (ADs) including Sjogren syndrome (SS). Here, we report a case of a young Chinese woman with recurrent optic neuritis who was diagnosed with asymptomatic SS and NMOSD.
A 22-year-old Chinese woman suffered from optic neuritis for 3 years. The main manifestation was recurrent loss of vision. The anti-aquaporin-4 antibody was positive in the cerebrospinal fluid, and she was diagnosed with NMOSD. Other laboratory tests revealed positive anti-SSA and anti-SSB antibodies, and labial gland biopsy showed lymphocytic infiltration. She also fulfilled the international criteria for SS.
On the basis of recurrent vision loss and laboratory examination, we defined the patient with SS accompanied by NMOSD.
When the patient first experienced vision loss, the corticosteroid treatment in the external hospital was effective, and her visual acuity improved significantly. However, in several later attacks, such treatment was no longer obviously effective. Considering the patient's condition, she was treated with corticosteroids, cyclophosphamide, and immunoglobulin therapy on admission.
The patient's visual acuity was increased to the right eye 20/800 and left eye finger counting when she was discharged from the hospital.
SS accompanied with NMOSD is common in clinical practice, and always with the positive Anti-AQP4 antibody as a potential biomarker. Patients with SS and NMOSD showed significant neurological symptoms and had a worse prognosis than SS patients with negative anti-AQP4 antibody because of cross-immunity between anti-SSA antibody and anti-AQP4 antibody. Rheumatologists and ophthalmologists should pay attention to this and perform appropriate tests.
视神经脊髓炎谱系障碍(NMOSD)患者,尤其是那些抗水通道蛋白4抗体呈阳性的患者,水通道蛋白4是一种在星形胶质细胞上表达的水通道,常伴有自身免疫性疾病(ADs),包括干燥综合征(SS)。在此,我们报告一例患有复发性视神经炎的年轻中国女性病例,该患者被诊断为无症状性SS和NMOSD。
一名22岁的中国女性患视神经炎3年。主要表现为反复视力丧失。脑脊液中抗水通道蛋白4抗体呈阳性,她被诊断为NMOSD。其他实验室检查显示抗SSA和抗SSB抗体呈阳性,唇腺活检显示淋巴细胞浸润。她也符合SS的国际诊断标准。
根据反复视力丧失和实验室检查,我们确定该患者患有伴有NMOSD的SS。
患者首次出现视力丧失时,在外院接受的皮质类固醇治疗有效,视力显著改善。然而,在随后的几次发作中,这种治疗不再明显有效。考虑到患者的病情,入院时对她采用了皮质类固醇、环磷酰胺和免疫球蛋白治疗。
患者出院时右眼视力提高到20/800,左眼能数指。
SS合并NMOSD在临床实践中很常见,抗水通道蛋白4抗体阳性始终是一种潜在的生物标志物。由于抗SSA抗体和抗水通道蛋白4抗体之间的交叉免疫,患有SS和NMOSD的患者表现出明显的神经症状,并且比抗水通道蛋白4抗体阴性的SS患者预后更差。风湿科医生和眼科医生应注意这一点并进行适当的检查。