Alhayali Mustafa
Internal Medicine/Rheumatology, Ibn Sina University for Medical and Pharmaceutical Sciences, Baghdad, IRQ.
Rheumatology and Medical Rehabilitation, Center of Spine and Joint Diseases, Baghdad, IRQ.
Cureus. 2024 Nov 23;16(11):e74301. doi: 10.7759/cureus.74301. eCollection 2024 Nov.
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative motor neuron disease that leads to a gradual loss of motor neurons manifesting as progressive weakness, dysarthria, and respiratory decline, with a relatively short life expectancy. Rheumatoid arthritis (RA) is an autoimmune disorder characterized by polyarthritis and affects multiple systems. Motor neuron involvement is rare in rheumatoid arthritis. Here, we report a unique case of a patient with an established diagnosis of ALS who later developed seropositive RA. A 58-year-old male from Baghdad presented to our center with polyarticular joint pain, stiffness, and swelling for about four months, the patient had a history of progressive neurological deficits. The final diagnosis was seropositive rheumatoid arthritis with concomitant amyotrophic lateral sclerosis. While the patient's joint symptoms responded well to methotrexate and prednisolone, he continued to experience a neurological decline. This is one of the few reported cases of concurrent ALS and RA, highlighting the complexity of managing overlapping neurodegenerative and autoimmune conditions.
肌萎缩侧索硬化症(ALS)是一种进行性神经退行性运动神经元疾病,会导致运动神经元逐渐丧失,表现为进行性肌无力、构音障碍和呼吸功能衰退,预期寿命相对较短。类风湿关节炎(RA)是一种以多关节炎为特征的自身免疫性疾病,会影响多个系统。运动神经元受累在类风湿关节炎中较为罕见。在此,我们报告一例独特病例,一名已确诊为ALS的患者后来发展为血清阳性RA。一名来自巴格达的58岁男性因多关节疼痛、僵硬和肿胀约四个月前来我院就诊,该患者有进行性神经功能缺损病史。最终诊断为血清阳性类风湿关节炎合并肌萎缩侧索硬化症。虽然患者的关节症状对甲氨蝶呤和泼尼松龙反应良好,但他仍持续出现神经功能衰退。这是为数不多的同时患有ALS和RA的报道病例之一,凸显了管理重叠的神经退行性疾病和自身免疫性疾病的复杂性。