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De Novo AL Amyloidosis in a Renal Allograft / 대한내과학회지
Korean Journal of Medicine ; : 545-549, 2016.
Article in Korean | WPRIM (Western Pacific) | ID: wpr-77224
Responsible library: 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.
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Main subject: Proteinuria / Biopsy / Incidence / Kidney Transplantation / Immunoglobulin Light Chains / Dyspnea / Electrophoresis / Allografts / Transplant Recipients / Heart Type of study: Incidence study / Prognostic study Limits: Humans Language: Korean Journal: Korean Journal of Medicine Year: 2016 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Proteinuria / Biopsy / Incidence / Kidney Transplantation / Immunoglobulin Light Chains / Dyspnea / Electrophoresis / Allografts / Transplant Recipients / Heart Type of study: Incidence study / Prognostic study Limits: Humans Language: Korean Journal: Korean Journal of Medicine Year: 2016 Document type: Article
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