摘要
最近的研究提示散发性包涵体肌炎的发病机制可能与免疫炎性反应、细胞变性、异常蛋白聚集、线粒体异常等有关,对于包涵体肌炎的诊断主要依赖病理诊断,免疫调节治疗可能有效。本文就包涵体肌炎发病机制的研究、临床表现及治疗等有关方面的最新进展进行了简要综述。
出处
《国际神经病学神经外科学杂志》
2009年第6期514-518,共5页
Journal of International Neurology and Neurosurgery
参考文献29
-
1Chou SM. Myxovirus-like structures in a case of human chronic polymyositis. Science, 1967, 158 ( 807 ) : 1453- 1455.
-
2Yunis E J, Samaha FJ. Inclusion body myositis. Lab Invest, 1971, 25(3) : 240-248.
-
3Carpenter S, Karpati G, HeIler I, et al. Inclusion body myosiris: a distinct variety of idiopathic inflammatory myopathy. Neurology, 1978, 28(1) : 8-17.
-
4Shamim EA, Rider LG, Pandey JP, et al. Differences in idiopathic inflammatory myopathy phenotypes and genotypes between Mesoamerican Mestizos and North American caucasians: ethnogeographic infl uences in the genetics and clinical expression of myositis. Arthritis Rheum, 2002, 46 ( 7 ) : 1885- 1893.
-
5Felice KJ, North WA. Inclusion body myositis in Connecticut: observations in 35 patients during an 8-year period. Medicine, 2001, 80(5): 320-327.
-
6Dalakas MC. Inflammatory, immune, and viral aspects of inclusion-body myositis. Neurology, 2006, 66 (2 Suppl 1 ) : S33 -S38.
-
7Askanas V, Engel WK. Inclusion-body myositis, a multifactorial muscle disease associated with aging: current concepts of pathogenesis. Curr Opin Rheumatol, 2007, 19 ( 6 ) : 550- 559.
-
8Delaunay A, Bromberg KD, Hayashi Y, et al. The ER- bound RING finger protein 5 ( RNF5/RMA 1 ) causes degenerative myopathy in transgenic mice and is deregulated in in- clusion body myositis. PLoS ONE, 2008 , 3 (2) : e1609.
-
9Fidzianska A, Rowinska- Marcinska K, Hausmanowa- Petrusewicz I. Coexistence of X-linked recessive Emery-Dreifuss muscular dystrophy with inclusion body myositis-like morphology. Acta Neuropathol, 2004, 107(3) : 197-203.
-
10Chou SM. Myxovims-like structures and accompanying nuclear changes in chronic polymyositis. Arch Pathol, 1968, 86 (6) : 649-658.
二级参考文献13
-
1孙琦,张平.包涵体肌炎(附1例报告并文献复习)[J].临床神经病学杂志,1996,9(4):240-241. 被引量:7
-
2崔丽英.肌电图在肌肉病诊断和鉴别诊断中应注意的问题[J].中国现代神经疾病杂志,2007,7(2):101-102. 被引量:5
-
3陈琳.肌肉活检在临床疾病诊断中的价值[J].中国现代神经疾病杂志,2007,7(2):103-106. 被引量:2
-
4蒲传强.炎性肌病的诊断与鉴别诊断[J].中国现代神经疾病杂志,2007,7(2):107-111. 被引量:5
-
5胡静,李娜,袁军辉,赵哲,沈宏锐,梅丽.包涵体肌炎的临床和病理分析[J].中华内科杂志,2007,46(8):658-660. 被引量:2
-
6段宏伟,郭玉璞.包涵体肌炎的临床研究进展[J].中华神经科杂志,1998,31(2):117-118. 被引量:5
-
7焉传祝,李大年,刘淑萍,吴金玲,郭斌,张雅萍.三例包涵体肌炎的临床与病理特点[J].中华神经科杂志,1998,31(3):168-170. 被引量:7
-
8周琳瑛,张文敏,陈莲云,王柠,梁平.散发型包涵体肌炎的临床与病理[J].电子显微学报,1999,18(3):332-335. 被引量:1
-
9张贵福,王华燕,李智文,王春木.包涵体肌炎的临床与肌活检特征[J].脑与神经疾病杂志,2001,9(3):188-189. 被引量:1
-
10闵丹琳,Anne Lacey,王鲁宁,沈定国.包涵体肌炎11例临床及组织病理报告[J].中华神经科杂志,2001,34(5):299-301. 被引量:7
共引文献12
-
1蒲传强.我国骨骼肌活体组织检查中存在的缺陷[J].中华神经科杂志,2012,45(1):3-5. 被引量:3
-
2钱倩,范慧,李娜.特发性炎性肌病分型诊断标准研究进展[J].国际神经病学神经外科学杂志,2013,40(2):176-179. 被引量:1
-
3陈金亮,田冉.散发性包涵体肌炎(附1例报告)[J].中风与神经疾病杂志,2013,30(12):1127-1128.
-
4陈淑媛,杜大勇.包涵体肌炎的研究现状[J].山东医药,2014,54(36):104-107. 被引量:1
-
5李珂,蒲传强,刘洁晓,毛燕玲,鲁向辉.老年散发性包涵体肌炎临床及病理表现[J].中国神经免疫学和神经病学杂志,2015,22(4):259-262. 被引量:3
-
6蒲传强,鲁向辉.注意识别镶边空泡肌病的病理、分类及基因[J].中华神经科杂志,2015,48(11):929-933. 被引量:4
-
7胡怀强,曹霞,李靖,王树才,曹秉振.散发性包涵体肌炎临床、电生理及病理特点[J].临床神经病学杂志,2017,30(1):58-60. 被引量:1
-
8苏飞飞,刘雪梅,魏晓晶,段晨晨,苗晶,于雪凡.结肠癌散发性包涵体肌炎1例报告[J].中国神经精神疾病杂志,2017,43(2):122-123.
-
9张英爽,董荣芳,孙阿萍,陈璐,刘向一,钟延丰,樊东升.成人炎症性肌肉病的临床病理特点:诊断标准及分类的新认识[J].北京医学,2017,39(5):444-449. 被引量:7
-
10蒲传强.特发性炎性肌病[J].中华神经科杂志,2019,52(5):410-422. 被引量:7
同被引文献15
-
1王敏,笪宇威,卢岩,徐敏,刘璐,贾建平.散发性包涵体肌炎临床病理分析[J].脑与神经疾病杂志,2011,19(5):389-392. 被引量:2
-
2吕海东,张三军,李增富,秦东香,钱琪,韩凯,马晓丽,宋学云,杨斌.包涵体肌炎的临床与病理特点(附2例报告)[J].临床神经病学杂志,2007,20(3):188-190. 被引量:4
-
3Nakanishi H, Koike H, Matsuo K, et al. Demographic lea tures of Japanese patients with sporadic inclusion body myosi tis: a single-center referral experienee[J]. Intern Med, 2013 52(3) :333-337.
-
4Cortese A, Machado P, Morrow J, et al. Longitudinal obser- vational study of sporadic inclusion body myositis: implications for clinical trials[J]. Neuromuscul Disord, 2013, 23 (5) : 404- 412.
-
5Clerici AM,Bono G,Delodovici ML,et al. A rare association of early-onset inclusion body myositis, rheumatoid arthritis and autoimmune thyroiditis: a case report and literature review [J]. Funct Neurol, 2013, 28(2) :127-132.
-
6Lindberg C, Oldfors A, Hedstrom A. Inclusion body myositis: peripheral nerve involvement. Combined morphological and electrophysiological studies on peripheral nerves [J]. J Neurol Sci, 1990, 99(2/3): 327-338.
-
7Allenbaeh Y, Benveniste O, Decostre V, et al. Quadriceps strength is a sensitive marker of disease progression in sporadic inclusion body myositis[J]. Neuromuscul Disord, 2012, 22 (11) :980-986.
-
8Finsterer J, Stollberger C, Kovacs GG. Asymptomatic hyper creatine-kinase-emia as sole manifestation of inclusion body myositis[J]. NeuroI Int, 2013, 5(2): 34-36.
-
9Greenberg SA, Pinkus JL, Amato AA. Nuclear membrane proteins are present with in rimmed vacuoles in inclusion body myositis[J]. Muscle Nerve, 2006, 34 (4): 406-416.
-
10Breithaupt M, Schmidt J. Update on treatment of inclusion body myositis[J]. Curr RheumatolRep, 2013, 15(5) :329.
引证文献3
-
1陈金亮,田冉.散发性包涵体肌炎(附1例报告)[J].中风与神经疾病杂志,2013,30(12):1127-1128.
-
2史秀丽,徐仿成,汪凯.以“麻木”起病伴甲减的包涵体肌炎临床特点分析[J].中国实用神经疾病杂志,2015,18(7):128-129.
-
3徐小敏,刘洋,王洵,魏有东.散发性包涵体肌炎1例报告[J].重庆医科大学学报,2017,42(10):1306-1307.
-
1叶廷军,刘会敏,陈泳莲,姜晓钟.巨噬细胞、肥大细胞免疫炎性反应和三叉神经脱髓鞘关系探讨(论著摘要)[J].中国神经免疫学和神经病学杂志,1999,6(4):281-282. 被引量:27
-
2李漪,袁云,高唯一,崔淑芳,吴晓燕.伴有智能减退的包涵体肌炎1例报告[J].中国神经精神疾病杂志,2002,28(2):147-148. 被引量:2
-
3胡怀强,曹霞,李靖,王树才,曹秉振.散发性包涵体肌炎临床、电生理及病理特点[J].临床神经病学杂志,2017,30(1):58-60. 被引量:1
-
4郭洁,巩忠影,任晓丽.散发性包涵体肌炎一例报告[J].实用心脑肺血管病杂志,2010,18(4):488-490. 被引量:1
-
5陈金亮,田冉.散发性包涵体肌炎(附1例报告)[J].中风与神经疾病杂志,2013,30(12):1127-1128.
-
6蒲传强.注意散发性包涵体肌炎的诊断[J].中华神经科杂志,2009,42(3):145-148. 被引量:13
-
7张强.阿尔茨海默病与免疫炎性反应[J].医学综述,2007,13(16):1250-1252. 被引量:6
-
8曹霞,王树才,常高峰,曹秉振.散发性包涵体肌炎二例报告[J].中国医师杂志,2008,10(7):1006-1007.
-
9唐政,曾彩红,姚小丹.肾病综合征的免疫调节治疗[J].肾脏病与透析肾移植杂志,1995,4(3):268-273.
-
10郑日亮,袁云.散发性包涵体肌炎的研究现状[J].中国现代神经疾病杂志,2007,7(6):540-542. 被引量:1