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Am J Dermatopathol ; 40(5): 337-341, 2018 May.
Article in English | MEDLINE | ID: mdl-28953013

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.


Subject(s)
Immunoglobulin kappa-Chains , Paraproteinemias/pathology , Adult , Female , Humans , Male
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