De Novo AL Amyloidosis in a Renal Allograft / 대한내과학회지
Korean Journal of Medicine
; : 545-549, 2016.
Article
en Ko
| WPRIM
| ID: wpr-77224
Biblioteca responsable:
WPRO
ABSTRACT
Amyloidosis is characterized by the extracellular deposition of amyloid in various tissues and organs, particularly the kidney and heart. The estimated incidence of systemic amyloidosis is at least 8 per million population per year. However, few cases of systemic amyloidosis in renal allografts have been reported. A stable renal transplant recipient was admitted with proteinuria and dyspnea on exertion. The M-peak was found on serum and urine protein electrophoresis, and lambda (λ) dominance was confirmed by serum and urine free-light-chain test. The patient was diagnosed with systemic amyloidosis of a renal allograft, by allograft biopsy, at 22 years after renal transplantation. We report a case of AL amyloidosis in a stable renal allograft and review the medical literature.
Palabras clave
Texto completo:
1
Índice:
WPRIM
Asunto principal:
Proteinuria
/
Biopsia
/
Incidencia
/
Trasplante de Riñón
/
Cadenas Ligeras de Inmunoglobulina
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Disnea
/
Electroforesis
/
Aloinjertos
/
Receptores de Trasplantes
/
Corazón
Tipo de estudio:
Incidence_studies
/
Prognostic_studies
Límite:
Humans
Idioma:
Ko
Revista:
Korean Journal of Medicine
Año:
2016
Tipo del documento:
Article