| Literature DB >> 16546597 |
Yasuyuki Fujita1, Yukiko Tsuji-Abe, Kazuko C Sato-Matsumura, Masashi Akiyama, Hiroshi Shimizu.
Abstract
We report the case of a 61-year-old Japanese man with IgG lambda-type multiple myeloma, who presented with nail dystrophy as the initial manifestation of systemic amyloidosis. Subsequently he developed bullous amyloidosis. This report documents these two rare signs of systemic amyloidosis and demonstrates the precise location of cutaneous blister formation and amyloid deposition by fluorescence antigen mapping and electron microscopy.Entities:
Mesh:
Year: 2006 PMID: 16546597 DOI: 10.1016/j.jaad.2005.12.031
Source DB: PubMed Journal: J Am Acad Dermatol ISSN: 0190-9622 Impact factor: 11.527