Stolz W, Ring J, Meurer M
Dermatologische Klinik und Poliklinik, Ludwig-Maximilians-Universität München.
Hautarzt. 1988 Jun;39(6):371-4.
The case of a 75-year-old female patient with angiomas and telangiectasia of the face and fingers mimicking Osler's disease (telangiectasia hereditaria hemorrhagica) is reported, in whom the presence of anticentromere antibodies and additional clinical signs led to the final diagnosis of CREST syndrome.
报告了一例75岁女性患者,其面部和手指出现血管瘤和毛细血管扩张,类似奥斯勒病(遗传性出血性毛细血管扩张症),该患者存在抗着丝点抗体及其他临床体征,最终诊断为CREST综合征。