Pippin Micah, Hanan Saad, Pawlichuk Danielle, Mays Dana
Family Medicine, LSUHS (Louisiana State University Health Sciences) Shreveport/Rapides Regional, Alexandria, USA.
Cureus. 2024 Jul 22;16(7):e65123. doi: 10.7759/cureus.65123. eCollection 2024 Jul.
Neuromyelitis optica (NMO), also known as Devic syndrome, is an autoimmune inflammatory and demyelinating disorder that affects the optic nerves and spinal cord. It is believed to be attributed to aquaporin-4 antibodies, a water channel expressed on astrocytes. It commonly presents with isolated or recurrent attacks of myelitis and optic neuritis. Intractable vomiting and hiccups may also be seen as symptoms. Acute treatment is often achieved with high-dose steroids and is imperative to prevent permanent central nervous system damage. Relapse prevention is achieved using long-term immunosuppression. This paper examines the case of an African-American female who presented with ascending lower extremity weakness.
视神经脊髓炎(NMO),也称为德维克综合征,是一种自身免疫性炎症性脱髓鞘疾病,会影响视神经和脊髓。据信这是由水通道蛋白4抗体引起的,水通道蛋白4是一种在星形胶质细胞上表达的水通道。它通常表现为孤立性或复发性脊髓炎和视神经炎发作。顽固性呕吐和打嗝也可能是症状。急性治疗通常采用大剂量类固醇,对于预防永久性中枢神经系统损伤至关重要。通过长期免疫抑制来预防复发。本文研究了一名出现下肢进行性无力的非裔美国女性的病例。