von der Helm D, Ring J, Schmoeckel C, Braun-Falco O
Dermatologische Klinik und Poliklinik Ludwig-Maximilians-Universität München.
Hautarzt. 1989 Mar;40(3):153-7.
A 66-year-old female patient developed within 2 years clinical symptoms of hyalinosis cutis et mucosae due to a plasmocytoma with monoclonal IgG-light-chain gammopathy. The clinical diagnosis was supported by light- and electron-microscope studies. The form of hyalinosis cutis et mucosae described by Urbach and Wiethe is a genetic disease with its onset in early childhood. For this reason, we propose the designation "acquired hyalinosis cutis et mucosae" for the case reported here.
一名66岁女性患者因浆细胞瘤伴单克隆IgG轻链丙种球蛋白病在2年内出现皮肤黏膜透明变性的临床症状。光镜和电镜研究支持了该临床诊断。Urbach和Wiethe描述的皮肤黏膜透明变性形式是一种始于儿童早期的遗传性疾病。因此,我们建议将此处报告的病例命名为“获得性皮肤黏膜透明变性”。