Cutaneous Light Chain Deposition Disease: A Report of 2 Cases and Review of the Literature.
Am J Dermatopathol
; 40(5): 337-341, 2018 May.
Article
en En
| 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.
Texto completo:
1
Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Paraproteinemias
/
Cadenas kappa de Inmunoglobulina
Límite:
Adult
/
Female
/
Humans
/
Male
Idioma:
En
Revista:
Am J Dermatopathol
Año:
2018
Tipo del documento:
Article
País de afiliación:
Alemania