|
腓骨肌萎缩症4例误诊分析并文献复习
|
Abstract:
目的:探讨腓骨肌萎缩症的不典型临床表现及误诊原因。方法:对我院误诊的1例腓骨肌萎缩症进行回顾性分析,并通过中国知网、万方医学网,输入“腓骨肌萎缩症、误诊”进行文献检索,查找到既往误诊3例,对4例患者的误诊原因进行分析。结果:4例患者分别被误诊为:干眼症(误诊时间2年)、原发性视神经萎缩(误诊34年)、慢性阻塞性肺疾病,慢性肺源性心脏病(误诊8年)及腰椎间盘突出并椎管狭窄症(误诊10年)。诊断明确后嘱患者注意休息,勿过度劳累,避免剧烈运动,给予口服甲钴胺、维生素B1、维生素C及针灸、理疗等治疗。经随访,患者症状均无明显改善,缓慢进展。结论:因本病早期临床表现不典型,医生对本病了解掌握不够,导致误诊率高。下一步应加强学习,拓宽知识面,提高对神经科少见疾病的认识。临床中应进行规范全面细致的查体,避免先入为主,要加强与相关科室的沟通,必要时进行会诊,集思广益。
Objective: To explore the atypical clinical manifestations and misdiagnosis reasons of peroneal muscular atrophy. Methods: A retrospective analysis was conducted on one misdiagnosed case of peroneal muscular atrophy in our hospital, and literature search was conducted by inputting “Peroneal muscular atrophy and misdiagnosis” through CNKI and Wanfang Medical Network. Three previous misdiagnosis cases were found, and the causes of misdiagnosis in four patients were analyzed. Result: Four patients were misdiagnosed as dry eye syndrome (misdiagnosed for 2 years), primary optic nerve atrophy (misdiagnosed for 34 years), chronic obstructive pulmonary disease, chronic pulmonary heart disease (misdiagnosed for 8 years), and lumbar disc herniation with spinal stenosis (misdiagnosed for 10 years). After the diagnosis was clear, all the patients were instructed to take a rest, avoid overwork and strenuous exercise. Oral mecobalamin, vitamin B1, vitamin C, acupuncture and moxibustion, physiotherapy and other treatments were given. After follow-up, the patients’ symptoms did not improve significantly, but progressed slowly. Conclusion: Due to atypical early clinical manifestations of this disease and insufficient understanding and mastery by doctors, the misdiagnosis rate is high. The next step is to strengthen learning, broaden knowledge, and improve understanding of rare neurological diseases. In clinical practice, standardized, comprehensive, and meticulous physical examinations should be conducted. We should avoid preconceptions. Communication with relevant departments should be strengthened, and consultations should be conducted if necessary to gather wisdom.
[1] | Zhang, H., Zhou, Z.W. and Sun, L. (2021) Aminoacyl-tRNA Synthetases in Charcot-Marie-Tooth Disease: A Gain or a Loss? Journal of Neurochemistry, 157, 351-369. https://doi.org/10.1111/jnc.15249 |
[2] | Yalcouye, A., Esoh K., Guida, L. and Wonkam, A. (2022) Current Profile of Charcot-Marie-Tooth Disease in Africa: A Systematic Review. Journal of the Peripheral Nervous System, 27, 100-112. https://doi.org/10.1111/jns.12489 |
[3] | 赵晨怡, 郜妞妞, 李茹, 等. 一例腓骨肌萎缩症误诊病例报道及鉴别诊断思考[J]. 中外女性健康研究, 2017(6): 97-98. |
[4] | 赵国柱. 腓骨肌萎缩症一例误诊[J]. 临床误诊误治, 2006, 19(8): 96. |
[5] | 郭司文, 安英俊, 李平, 等. 腓骨肌萎缩症导致呼吸衰竭1例[J]. 中国实用医药, 2016, 11(24): 215-216. |
[6] | 洪道俊, 张玉生. Charcot-Marie-Tooth病的诊治[J]. 暨南大学学报(自然科学与医学版), 2014, 35(5): 432-438. |
[7] | 朱琳, 胡静. Charcot-Marie-Tooth病的研究与诊断进展[J]. 神经损伤与功能重建, 2011, 6(5): 320-327. https://doi.org/10.3870/sisscj.2011.05.002 |
[8] | 张捷君, 黄顺祥, 赵华栋, 等. 腓骨肌萎缩症四种最常见基因亚型的电生理特点分析[J]. 中华神经科杂志, 2019, 52(1): 26-33. |
[9] | 郭鹏, 翟晖, 宋福聪. 腓骨肌萎缩症临床表现、基因分型和分子发病机制研究进展[J]. 中风与神经疾病杂志, 2013, 30(10): 953-955. |
[10] | 王敏, 笪宇威, 张新卿, 等. 腓骨肌萎缩症伴发POEMS综合征一例报告[J]. 神经疾病与精神卫生, 2014, 14(6): 643-644. |
[11] | 张如旭, 唐北沙, 等. 腓骨肌萎缩症1A型的临床、神经电生理和疾病基因突变分析[J]. 临床神经病学杂志, 2003, 16(6): 324-326. |
[12] | 张敏, 杨仕林, 陈淑芬, 等. 以短暂性脑缺血样发作伴可逆性脑白质病变起病的X连锁腓骨肌萎缩症1型一例[J]. 中华医学遗传学杂志, 2021, 38(4): 405-406. https://doi.org/10.3760/cma.j.cn511374-20200218-00087 |
[13] | 王辉, 安冉, 徐严明. 一例GJB1基因新变异导致的X连锁腓骨肌萎缩症[J]. 中华医学遗传学杂志, 2020, 37(5): 594. https://doi.org/10.3760/cma.j.issn.1003-9406.2020.05.027 |
[14] | 刘洋, 徐小敏, 魏有东. GJBl基因突变的X连锁腓骨肌萎缩症一例[J]. 临床内科杂志, 2017, 34(10): 712. |
[15] | 梁有龙. 伴发可逆性后部脑白质病变的X连锁腓骨肌萎缩症的临床特点和基因突变分析[D]: [硕士学位论文]. 南宁: 广西医科大学, 2019. |
[16] | 林志强, 李小波, 黄顺祥, 等. 中国人山梨醇脱氢酶基因相关腓骨肌萎缩症的基因型-表型分析[J]. 中华神经科杂志, 2020, 53(11): 882-887. |
[17] | 张丽. 240例干眼症患者临床特征分析[J]. 中国现代药物应用, 2019, 13(13): 23-25. |
[18] | 薛慧. 玻璃酸钠滴眼液联合贝复舒滴眼液治疗干眼症的疗效观察[J]. 中国现代药物应用, 2021, 15(1): 196-198. https://doi.org/10.14164/j.cnki.cn11-5581/r.2021.01.089 |
[19] | 黄锐升, 林丽敏, 金泰, 等. 伴发于良性特发性眼睑痉挛的干眼病的眼表特征分析[J]. 中国处方药, 2021, 19(3): 151-152. |