Mosconi Sandro, Streit Markus, Brönimann Marcel, Braathen Lasse R
Dermatological Clinic, Inselspital, University of Berne, Switzerland.
Dermatology. 2002;205(2):204-6. doi: 10.1159/000063916.
We report a case of a 30-year-old Caucasian patient with progressive sclerosis of the skin mainly on the upper limbs which was diagnosed as eosinophilic fasciitis (Shulman syndrome). Circulating antibodies against Borrelia burgdorferi were detected. The association of B. burgdorferi infection with eosinophilic fasciitis is discussed.
我们报告一例30岁的白种人患者,其主要在上肢出现进行性皮肤硬化,被诊断为嗜酸性筋膜炎(舒尔曼综合征)。检测到了抗伯氏疏螺旋体的循环抗体。本文讨论了伯氏疏螺旋体感染与嗜酸性筋膜炎的关联。