Clinical features of myasthenia gravis in southern China: a retrospective review of 2,154 cases over 22 years

被引:54
作者
Huang, X. [1 ]
Liu, W. B. [1 ]
Men, L. N. [1 ]
Feng, H. Y. [1 ]
Li, Y. [1 ]
Luo, C. M. [1 ]
Qiu, L. [1 ]
机构
[1] Sun Yat Sen Uni, Dept Neurol, Affiliated Hosp 1, Guangzhou 510080, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Clinical features; Myasthenia gravis; Autoimmune disease; Family myasthenia gravis; EPIDEMIOLOGY; MORTALITY;
D O I
10.1007/s10072-012-1157-z
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The objectives of the study are to study the clinical features of myasthenia gravis in southern China. A retrospective study was carried out on all patients who were diagnosed with myasthenia gravis at the First Affiliated Hospital of Sun Yat-sen University during 1987-2009. Of the 2,154 myasthenia gravis patients, the gender ratio (male:female) was 1:1.15. The median age at onset was 18 years. There was a single peak distribution of age at onset, and 44.8 % were children (a parts per thousand currency sign14 years) at first onset. 1,766 patients (82.0 %) only had ocular symptoms at onset. 1,451 patients (67.4 %) were classified as Osserman grade I. 250 unselected patients received anti-acetylcholine receptor antibodies test, in which only 51.2 % were positive. Computed tomography scan/magnetic resonance Imaging of chest were done in 1,354 patients, of which 899 patients (66.4 %) had thymic hyperplasia and 201(14.8 %) had thymoma. There were 150 patients (7.0 %) with myasthenia gravis combined with other autoimmune diseases, in which hyperthyroidism was most common (84 %). 189 (8.8 %) patients experienced 267 episodes of crisis. The rate of family myasthenia gravis was 1.6 % (35/2,154). In conclusion, the clinical features and demography of myasthenia gravis patients in this study are significantly different from prior studies on other regions and ethnic groups.
引用
收藏
页码:911 / 917
页数:7
相关论文
共 23 条
[1]   Thymomas: a cytological and immunohistochemical study, with emphasis on lymphoid and neuroendocrine markers [J].
Alexiev, Borislav A. ;
Drachenberg, Cinthia B. ;
Burke, Allen P. .
DIAGNOSTIC PATHOLOGY, 2007, 2 (1)
[2]   Mortality and survival in myasthenia gravis: a Danish population based study [J].
Christensen, PB ;
Jensen, TS ;
Tsiropoulos, I ;
Sorensen, T ;
Kjaer, M ;
Hojer-Pedersen, E ;
Rasmussen, MJK ;
Lehfeldt, E .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1998, 64 (01) :78-83
[3]  
Cui LY, 1994, CLIUN NEUROL, V1, P65
[4]   Epidemiological study of myasthenia gravis in the province of Reggio Emilia, Italy [J].
Guidetti, D ;
Sabadini, R ;
Bondavalli, M ;
Cavaletti, S ;
Lodesani, M ;
Mantegazza, R ;
Cosi, F .
EUROPEAN JOURNAL OF EPIDEMIOLOGY, 1998, 14 (04) :381-387
[5]   Myasthenia gravis: Recommendations for clinical research standards (Reprinted from Neurology, vol 55, pg 16-23, 2000) [J].
Jaretzki, A ;
Barohn, RJ ;
Ernstoff, RM ;
Kaminski, HJ ;
Keesey, JC ;
Penn, AS ;
Sanders, DB .
ANNALS OF THORACIC SURGERY, 2000, 70 (01) :327-334
[6]   Treatment and outcome of myasthenia gravis: retrospective multi-centor analysis of 470 Japanese patients, 1999-2000 [J].
Kawaguchi, N ;
Kuwabara, S ;
Nemoto, Y ;
Fukutake, T ;
Satomura, Y ;
Arimura, K ;
Osame, M ;
Hattori, T .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2004, 224 (1-2) :43-47
[7]  
Kirmani JF, 2004, CURR TREAT OPTION NE, V6, P13
[8]  
Lok W, 2003, NEUROL J SE ASIA, V8, P35
[9]   Epidemiology of seropositive myasthenia gravis in Greece [J].
Poulas, K ;
Tsibri, E ;
Kokla, A ;
Papanastasiou, D ;
Tsouloufis, T ;
Marinou, M ;
Tsantili, P ;
Papapetropoulos, T ;
Tzartos, SJ .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2001, 71 (03) :352-356
[10]   Myasthenia gravis: a population based epidemiological study in Cambridgeshire, England [J].
Robertson, NP ;
Deans, J ;
Compston, DAS .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1998, 65 (04) :492-496