肌萎缩侧索硬化
医学
大疱性类天疱疮
发病机制
抗原
皮肤病科
人口
病理
抗体
免疫学
疾病
环境卫生
作者
Olivier Chosidow,Valérie Doppler,Gilbert Bensimon,P. Joly,François Salachas,Lucette Lacomblez,Cathérine Prost,William Camu,Camille Françès,S. Herson,Vincent Meininger
出处
期刊:Archives of Dermatology
[American Medical Association]
日期:2000-04-01
卷期号:136 (4)
被引量:54
标识
DOI:10.1001/archderm.136.4.521
摘要
Background
Bullous pemphigoid (BP) occurs in many patients with multiple sclerosis. Isolated cases of BP in patients with other neurological disorders further support a pathogenic association between cutaneous and neurological diseases. Any description of BP in patients with amyotrophic lateral sclerosis is lacking. Observations
We studied a French population of 168 patients with typical amyotrophic lateral sclerosis. Among these, 3 had clinical and histological features of BP. The mean age of the patients was 54 years. None was known to have autoimmune disorders. Results of immunoblot analysis disclosed both anti-BP antigen 1 and anti-BP antigen 2 antibodies. Conclusions
Bullous pemphigoid seems to be unexpectedly associated with amyotrophic lateral sclerosis. On the basis of the cases presented herein, we discuss the epidemiological significance of the association and the possible interrelation between BP antigen 1 and neurofilaments in the pathogenesis of both disorders.
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