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Development of systemic λ-light chain amyloidosis in a patient with γ-heavy chain deposition disease during long-term follow-up

Nephrology Dialysis Transplantation (2005) 20(2) 434-437
DOI: 10.1093/ndt/gfh545
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Abstract

In summary, we have presented an unusual case of a patient who developed HCDD and later systemic AL amyloidosis during long-term follow-up. This case reveals a previously unreported association between AL amyloidosis and HCDD. © ERA-EDTA 2005; all rights reserved.

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Komatsuda, A., Maki, N., Wakui, H., Ohtani, H., Hatakeyama, T., Yasuda, T., … Sawada, K. I. (2005). Development of systemic λ-light chain amyloidosis in a patient with γ-heavy chain deposition disease during long-term follow-up. Nephrology Dialysis Transplantation, 20(2), 434–437. https://doi.org/10.1093/ndt/gfh545

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