Sugisaki Kota, Saito Rie, Takagi Tadayuki, Shio Kiori, Shioya Yasuo, Fukaya Etsuko, Iwadate Haruyo, Sekine Hideharu, Orikasa Hiroshi, Kobayashi Hiroko, Watanabe Hiroshi, Sato Yukio
Department of Internal Medicine II, Fukushima Medical University School of Medicine, 1 Hikarigaoka, Fukushima, 960-1295, Japan.
Mod Rheumatol. 2005;15(1):56-61. doi: 10.1007/s10165-004-0356-8.
We report a case of HLA-B52-positive Behçet disease accompanied by multiarterial lesions. A 24-year-old woman was suffering from sporadic high fever and recurrent oral and genital ulcers, and laboratory data revealed severe inflammation. A diagnosis of Behçet disease was made. Magnetic resonance angiography, ultrasound study, and computed tomographic angiography demonstrated multiarterial lesions that had caused no symptoms. These noninvasive examinations were extremely useful in evaluating asymptomatic early vascular lesions.
我们报告一例伴有多动脉病变的HLA - B52阳性白塞病。一名24岁女性患有散发性高热、复发性口腔和生殖器溃疡，实验室检查显示有严重炎症。诊断为白塞病。磁共振血管造影、超声检查和计算机断层血管造影显示存在未引起任何症状的多动脉病变。这些非侵入性检查在评估无症状早期血管病变方面极其有用。
