Publications by authors named "Mizuki Kyoda"

Article Synopsis
  • Crystalglobulin-induced nephropathy is a rare disease characterized by the accumulation of crystallized monoclonal immunoglobulins in the kidney's filtering system.
  • A patient presented with symptoms such as skin ulcers, protein in urine, and kidney dysfunction, leading to renal and skin biopsies.
  • The diagnosis was confirmed through advanced techniques, including mass spectrometry, highlighting the importance of specialized pathology methods for identification of this condition.
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Background: The clinical characteristics and treatment of patients with antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) after initiating chronic hemodialysis remain unknown.

Methods: We retrospectively enrolled 11 adult patients with AAV receiving chronic hemodialysis in our hospital from 2000-2016. We collected data describing each patient's clinical findings and treatment before and after initiating hemodialysis.

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Renal disease is a common complication of rheumatoid arthritis (RA) and can occur secondary to RA or be induced by therapeutic agents. Recently, glomerular deposition of galactose-deficient IgA1 (Gd-IgA1) was identified as a feature of primary IgA vasculitis with nephritis (IgA-VN). We herein report a case of IgA-VN in an RA patient whose disease activity was controlled by treatment with etanercept.

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A 41-year-old woman developed nephrotic syndrome at the age of 32 and was diagnosed with minimal change nephrotic syndrome based on a renal biopsy. Although remission was achieved with administration of prednisolone (PSL) and cyclosporine, the nephrotic syndrome recurred. She was also started on rituximab (RTX).

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