Aher Priyanka S, Bhavsar Deepaswi, Toshniwal Sumit, Bora Riddhi A, Jagadish Rohan
Ophthalmology, Dr. D. Y. Patil Medical College and Hospital, Pune, IND.
Ophthalmology, Dr. D. Y. Patil Medical College, Hospital and Research Center, Pune, IND.
Cureus. 2024 Aug 21;16(8):e67408. doi: 10.7759/cureus.67408. eCollection 2024 Aug.
A rare demyelinating syndrome, known as neuromyelitis optica, is characterized by optic neuritis and transverse myelitis. A 27-year-old female presented to the eye department, with complaints of sudden progressive diminution of vision in both eyes (left eye more than right eye), acutely not being able to move both her eyes, double vision on lateral gazes with chronic dryness and irritation. Examination revealed restricted extraocular movements in all gazes. Magnetic resonance imaging of orbit showed retrobulbar optic neuritis. Blood tests revealed positive neuromyelitis optica myelin oligodendrocyte glycoprotein antibodies after which diagnosis of neuromyelitis optica was made.
一种罕见的脱髓鞘综合征,称为视神经脊髓炎,其特征为视神经炎和横贯性脊髓炎。一名27岁女性到眼科就诊,主诉双眼视力突然进行性下降(左眼比右眼更严重),急性起病时双眼不能活动,向外侧注视时出现复视,伴有慢性眼干和眼刺激症状。检查发现所有注视方向的眼球运动均受限。眼眶磁共振成像显示球后视神经炎。血液检查显示视神经脊髓炎髓鞘少突胶质细胞糖蛋白抗体呈阳性,据此作出视神经脊髓炎的诊断。