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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.
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Texto completo: 1 Índice: WPRIM Asunto principal: Proteinuria / Biopsia / Incidencia / Trasplante de Riñón / Cadenas Ligeras de Inmunoglobulina / 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
Texto completo: 1 Índice: WPRIM Asunto principal: Proteinuria / Biopsia / Incidencia / Trasplante de Riñón / Cadenas Ligeras de Inmunoglobulina / 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