Behcet disease - case report and review

被引：0
作者：
Romanska-Gocka, Krystyna [1 ,2 ]
Gocki, Jacek [3 ,4 ]
Placek, Waldemar [1 ,2 ]
Uchanska, Grazyna [1 ,2 ]
机构：
[1] Uniwersytetu Mikolaja Kopernika Toruniu, Katedra Dermatol Chorob Przenoszonych Droga Picio, Coll Medicum Ludwika Rydygiera Bydgoszczy, PL-85096 Bydgoszcz, Poland
[2] Uniwersytetu Mikolaja Kopernika Toruniu, Klin Dermatol Chorob Przenoszonych Droga Piciowa, Coll Medicum Ludwika Rydygiera Bydgoszczy, PL-85096 Bydgoszcz, Poland
[3] Uniwersytetu Mikolaja Kopernika Toruniu, Katedra Alergol Immunol & Chorob Wewnetrznych, Coll Medicum Ludwika Rydygiera Bydgoszczy, PL-85096 Bydgoszcz, Poland
[4] Uniwersytetu Mikolaja Kopernika Toruniu, Klin Alergol Immunol & Chorob Wewnetrznych, Coll Medicum Ludwika Rydygiera Bydgoszczy, PL-85096 Bydgoszcz, Poland
来源：
POSTEPY DERMATOLOGII I ALERGOLOGII | 2009年 / 26卷 / 04期
关键词：
Behcet disease; symptoms; diagnosis; treatment; ULCERS;
D O I：
暂无
中图分类号：
R392 [医学免疫学];
学科分类号：
100102 ;
摘要：
We report a rare case of Behcet's disease in a Caucasian man. Behcet's disease is a chronic recurrent generalized vasculitis whose manifestation seems to be dependent on genetic predisposition triggered by environmental factors. It occurs endemically in central and eastern Asia Dermatological symptoms are most common, including recurrent oral and genital aphthous ulcers. Severe ocular inflammation can lead to permanent impairment of vision. The involvement of other organ systems can potentially lead to life-threatening complications. We discuss the course of the disease, the clinical symptoms, the diagnostic criteria and methods of treatment.
引用
收藏
页码：224 / 228
页数：5
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