摘要
Ankylosing spondylitis （AS）, which primarily affects the sacroiliac joints, spine, and enthuses, is a chronic inflammatory rheumatic disorder. Acute anterior uveitis is the most common ophthalmologic involvement, whereas optic neuritis （ON） rarely coexists with AS.r^j ON is an immune-mediated inflammation of the optic nerve, which could be the initiated symptom of multiple sclerosis （MS） or neuromyelitis optica （NMO）. Bilateral simultaneous ON with long enhanced optic nerve lesions in magnetic resonance imaging （MRI） was considered as features of NMO spectrum disorders （NMOSDs）. However, comprehensive review of the current literature showed little evidence of AS as an accompanied autoimmune condition in NMO,121 and the specific biomarker aquaporin-4 antibody （AQP4-Ab） was negative in our patient. In the current report, we present the first case of ON with active AS in a Chinese male patient. The association between the two diseases remains to be evaluated.
Ankylosing spondylitis （AS）, which primarily affects the sacroiliac joints, spine, and enthuses, is a chronic inflammatory rheumatic disorder. Acute anterior uveitis is the most common ophthalmologic involvement, whereas optic neuritis （ON） rarely coexists with AS.r^j ON is an immune-mediated inflammation of the optic nerve, which could be the initiated symptom of multiple sclerosis （MS） or neuromyelitis optica （NMO）. Bilateral simultaneous ON with long enhanced optic nerve lesions in magnetic resonance imaging （MRI） was considered as features of NMO spectrum disorders （NMOSDs）. However, comprehensive review of the current literature showed little evidence of AS as an accompanied autoimmune condition in NMO,121 and the specific biomarker aquaporin-4 antibody （AQP4-Ab） was negative in our patient. In the current report, we present the first case of ON with active AS in a Chinese male patient. The association between the two diseases remains to be evaluated.
