- Koji Shinoda
Department of Neurology, Neurological Institute, Graduate School of Medical Sciences, Kyushu University, Japan
- Takuya Matsushita
Department of Clinical Neuroimmunology, Graduate School of Medical Sciences, Kyushu University, Japan
- Konosuke Furuta
Department of Neurology, Neurological Institute, Graduate School of Medical Sciences, Kyushu University, Japan
- Noriko Isobe
Department of Neurology, Neurological Institute, Graduate School of Medical Sciences, Kyushu University, Japan
- Tomomi Yonekawa
Department of Neurology, Neurological Institute, Graduate School of Medical Sciences, Kyushu University, Japan
- Yasumasa Ohyagi
Department of Neurology, Neurological Institute, Graduate School of Medical Sciences, Kyushu University, Japan
Abstract
This report describes, for the first time, an occurrence of wall-eyed bilateral internuclear ophthalmoplegia (WEBINO) in a 19-year-old female with neuromyelitis optica (NMO) spectrum disorder, who had anti-aquaporin-4 (AQP4) antibody. A high signal intensity lesion on T2-weighted MRI was detected in the midbrain tegmentum adjacent to the aqueduct, and presumably involved the medial longitudinal fasciculus bilaterally at the caudal levels. Plasma exchange resolved both WEBINO syndrome and the midbrain lesion. Although WEBINO syndrome is occasionally reported in multiple sclerosis patients, diagnosis of NMO should not be excluded in patients with WEBINO syndrome, because AQP4 is expressed abundantly around the periaqueductal region.
Read More: Wall-eyed bilateral internuclear ophthalmoplegia (WEBINO) syndrome in a patient with neuromyelitis optica spectrum disorder and anti-aquaporin-4 antibody — Mult Scler