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[Acquired hyalinosis cutis et mucosae in plasmacytoma with monoclonal IgG-lambda gammopathy]
D von der Helm1, J Ring, C Schmoeckel
1Dermatologische Klinik und Poliklinik Ludwig-Maximilians-Universität München.
Abstract:
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.