Nalini Atchayaram, Gourie-Devi Mandavilli, Thennarasu Kandavel, Ramalingaiah Aravinda Hanumanthapura
Department of Neurology, National Institute of Mental Health and Neurosciences , Bangalore , India.
Amyotroph Lateral Scler Frontotemporal Degener. 2014 Sep;15(5-6):457-65. doi: 10.3109/21678421.2014.903976. Epub 2014 May 22.
Our objective was to study the clinical characteristics and natural history of monomelic amyotrophy (MMA). We used a retrospective study of 279 patients diagnosed to have either upper (Hirayama disease) or lower limb MMA. Results showed that brachial MMA (BMMA) occurred in 224 patients (male:female, 9:1). Mean age of onset was 19.5 ± 4.18 years. Progression occurred over less than five years in the majority (95.9%) of patients. Duration at the last follow-up was: up to five years in 61.4%, 5-10 in 21.3%, 10-15 in 7.2%, > 15 years in 10.1%. MRI showed asymmetrical lower cervical cord atrophy in 44.6% of patients. Crural MMA (CMMA) occurred in 55 patients (male:female, 13:1). Mean age of onset was 21.38 ± 5.3 years. Similar to BMMA, most cases (65.5%) had onset between 15 and 25 years of age. Total duration of illness at the last follow-up was up to five years in 52.7%, 10 and beyond in 47.3%. In conclusion, a large cohort of patients with monomelic amyotrophy seen over 35 years (1976-2010) is described. Study data support the clinical findings and its natural history with long term follow-up, and the findings emphasize that monomelic amyotrophy is a 'benign' condition with a self-limiting course.
我们的目的是研究单肢肌萎缩症(MMA)的临床特征和自然病程。我们对279例被诊断为上肢(平山病)或下肢MMA的患者进行了回顾性研究。结果显示,224例患者发生了臂丛型MMA(BMMA)(男∶女为9∶1)。平均发病年龄为19.5±4.18岁。大多数患者(95.9%)在不到5年的时间里病情进展。最后一次随访时的病程为:61.4%的患者病程达5年,21.3%的患者病程为5至10年,7.2%的患者病程为10至15年,10.1%的患者病程超过15年。MRI显示44.6%的患者存在下颈髓不对称萎缩。55例患者发生了小腿型MMA(CMMA)(男∶女为13∶1)。平均发病年龄为21.38±5.3岁。与BMMA相似,大多数病例(65.5%)发病年龄在15至25岁之间。最后一次随访时的总病程为:52.7%的患者病程达5年,47.3%的患者病程为10年及以上。总之,本文描述了35年(1976 - 2010年)间大量的单肢肌萎缩症患者队列。研究数据通过长期随访支持了临床发现及其自然病程,这些发现强调单肢肌萎缩症是一种具有自限性病程的“良性”疾病。