Kumar Shanmugam Mahesh, Venkatraman Vaishali, Kowsalya Akkayasamy, Narayanamoorthy Jayasri, Jayasudha Marappan
Department of Neuro-Ophthalmology, Aravind Eye Hospital, Madurai, Tamil Nadu, India.
Oman J Ophthalmol. 2022 Nov 2;15(3):366-369. doi: 10.4103/ojo.ojo_65_21. eCollection 2022 Sep-Dec.
Acute optic neuritis (ON) is caused by variety of complex disorders that can be differentiated with the help of history, radiology, and serology. Identification of nonneurological symptoms that occur before the demyelinating event aids in timely diagnosis and prevention of further neurological attacks. We describe a case of unilateral ON with a history of intractable hiccups, nausea, and vomiting, wherein the possibility of area postrema syndrome (APS) was overlooked until the development of visual symptoms. APS recently identified as a hallmark of neuromyelitis optica spectrum disorder is a rare neurologic cause of gastrointestinal symptoms. This atypical presentation of APS results from autoantibodies directed against the aquaporin-4 rich sites, such as area postrema. This case brings to light the importance of eliciting history of intractable hiccups, nausea, and vomiting in a patient with ON. Despite being a commonly encountered symptom, it may rarely raise a suspicion for neuromyelitis optica.
急性视神经炎(ON)由多种复杂疾病引起,可借助病史、放射学和血清学进行鉴别。识别脱髓鞘事件之前出现的非神经症状有助于及时诊断并预防进一步的神经发作。我们描述了一例单侧视神经炎患者,该患者有顽固性呃逆、恶心和呕吐病史,在出现视觉症状之前,最后区综合征(APS)的可能性一直被忽视。APS最近被确定为视神经脊髓炎谱系障碍的一个标志,是胃肠道症状的一种罕见神经病因。APS的这种非典型表现是由针对富含水通道蛋白4的部位(如最后区)的自身抗体引起的。该病例揭示了在视神经炎患者中询问顽固性呃逆、恶心和呕吐病史的重要性。尽管这些症状很常见,但很少会引发对视神经脊髓炎的怀疑。