Literature DB >> 16546597

Nail dystrophy and blisters as sole manifestations in myeloma-associated amyloidosis.

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.

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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


  3 in total

1.  [Unusual skin alterations in a 72-year-old patient with multiple myeloma].

Authors:  C Hart; S Wurm; C Hafner; R Andreesen; M Grube
Journal:  Internist (Berl)       Date:  2012-04       Impact factor: 0.743

Review 2.  [Hereditary and non-hereditary cutaneous amyloidoses].

Authors:  S Schreml; J Schroeder; F Eder; R M Szeimies; M Landthaler; P Babilas
Journal:  Pathologe       Date:  2009-05       Impact factor: 1.011

3.  Renal-limited AL amyloidosis - a diagnostic and management dilemma.

Authors:  Kar Wah Fuah; Christopher Thiam Seong Lim
Journal:  BMC Nephrol       Date:  2018-11-06       Impact factor: 2.388

  3 in total

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