In:
The American Journal of Dermatopathology, Ovid Technologies (Wolters Kluwer Health), Vol. 40, No. 5 ( 2018-05), p. 337-341
Abstract:
Light chain deposition disease (LCDD) is a rare systemic disorder with deposition of mostly monoclonal amorphous nonamyloid light chains in multiple organs. Renal involvement with rapidly progressing renal failure presents the dominant manifestation of LCDD. Approximately 20%–30% of patients show symptomatic cardiac or liver involvement. Cutaneous manifestations are extremely rare with only a few published cases. We report 2 additional cases of cutaneous LCDD without detectable systemic disease.
Type of Medium:
Online Resource
ISSN:
0193-1091
DOI:
10.1097/DAD.0000000000000991
Language:
English
Publisher:
Ovid Technologies (Wolters Kluwer Health)
Publication Date:
2018
detail.hit.zdb_id:
2041296-4