We report 3 patients with nephrotic syndrome ascribed to primary systemic AL amyloidosis that were successfully treated with VAD (vincristine, doxorubiein and dexamethasone) alone. M-protein in serum disappeared soon after VAD, and nephrotic syndrome gradually improved in parallel with a decrease in daily protein excretion in urine. Long-term follow-up of these patients showed neither relapse of nephrotic syndrome nor reappearance of M-protein. High-dose melphalan followed by autologous stem cell support is a standard therapy for primary systemic AL amyloidosis, but in high-risk cases for this treatment, such as elderly patients and those with multiple organ involvement, VAD might be a therapeutic option. © 2008 The Japanese Society of Internal Medicine.
CITATION STYLE
Matsuda, M., Gono, T., Katoh, N., Yoshida, T., Tazawa, K. I., Shimojima, Y., … Ikeda, S. I. (2008). Nephrotic syndrome due to primary systemic AL amyloidosis, successfully treated with VAD (vincristine, doxorubicin and dexamethasone) alone. Internal Medicine, 47(6), 543–549. https://doi.org/10.2169/internalmedicine.47.0709
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