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Article
Correction to: Combined light chain crystalline tubulopathy, podocytopathy, and histiocytosis associated with Bence–Jones κ protein diagnosed via immuno-electron microscopy
A correction to this paper has been published: https://doi.org/10.1007/s13730-021-00596-9
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Article
Combined light chain crystalline tubulopathy, podocytopathy, and histiocytosis associated with Bence–Jones κ protein diagnosed via immuno-electron microscopy
We herein report a case of a combined crystalline light chain tubulopathy, podocytopathy, histiocytosis, and cast nephropathy in a patient with monoclonal gammopathy of renal significance (MGRS). A 66-year-old...
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Article
Combined IgG4κ and IgG1λ deposition in the glomerular and tubular basement membrane accompanied by autoimmune neutropenia (AIN) and immune thrombocytopenia (ITP)
A 48-year-old male was admitted to our hospital with nephrotic syndrome. Light-microscopic examination of a renal biopsy specimen showed almost normal glomerular appearance, however, immunofluorescence examina...
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Article
A case of adult Dent disease in Japan with advanced chronic kidney disease
Dent disease is an inherited tubulopathy caused by a mutation in the CLCN5 chloride channel gene. In cases of Dent disease in Japan (Japanese Dent, J-Dent), renal function is generally preserved and rarely progre...
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Article
Cyclosporine A-Mediated renal lesion in a child with intractable proteinuria
The histopathological observation of an 8-year-old boy who received cyclosporine A (CyA) for the treatment of persistent proteinuria is presented. In the renal biopsy specimen, typical CyA cytotoxic changes, ...
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Article
Staphylococcus aureus-associated nephritis with histologic features resembling hemolytic uremic syndrome
A case that revealed the clinical and histologic features of superantigen-related nephritis and hemolytic uremic syndrome is reported. The patient was admitted with purulent arthritis due toStaphylococcus aureus ...