Dandu Vasuki, Siddamreddy Suman, Meegada Sreenath, Muppidi Vijayadershan, Challa Tejo
Neurology, Baptist Health Medical Center, Little Rock, USA.
Internal Medicine, Baptist Health Medical Center, North Little Rock, USA.
Cureus. 2020 Feb 20;12(2):e7058. doi: 10.7759/cureus.7058.
Neuromyelitis optica (NMO) is a disease of central nervous system, characterized by demyelination and axonal damage mostly involving optic nerves and spinal cord. Usually these patients present with symptoms related to optic neuritis or myelitis with a typical relapsing course. Some patients present with less common symptoms involving brain stem like nausea and vomiting, especially those involving area postrema (AP) located in dorsal medulla. International panel for NMO diagnosis revised criteria in 2015 and came up with a unifying term NMO spectrum disorders (NMOSD) instead of NMO. Patients with NMO having AP involvement are grouped under area postrema syndrome (APS). Usually patients with AP symptoms also have neurological symptoms upon presentation. Here we present a rare case of an NMO who presented with isolated APS with no other neurological symptoms.
视神经脊髓炎(NMO)是一种中枢神经系统疾病,其特征是脱髓鞘和轴突损伤,主要累及视神经和脊髓。通常这些患者会出现与视神经炎或脊髓炎相关的症状,并伴有典型的复发病程。一些患者会出现涉及脑干的较罕见症状,如恶心和呕吐,尤其是那些累及位于延髓背侧的最后区(AP)的患者。2015年,国际NMO诊断小组修订了标准,并提出了一个统一的术语——视神经脊髓炎谱系障碍(NMOSD),而非NMO。患有AP受累的NMO患者被归类为最后区综合征(APS)。通常,出现AP症状的患者在就诊时也会有神经症状。在此,我们报告一例罕见的NMO病例,该患者仅表现为孤立的APS,无其他神经症状。