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A Case of IgA kappa Light Chain Deposition Disease and Combined Adult Fanconi Syndrome with Auer rod-like Intracytoplasmic Inclusions in Plasma Cells and Proximal Renal Tubular Cells / 대한진단검사의학회지
The Korean Journal of Laboratory Medicine ; : 248-252, 2007.
Article in Korean | WPRIM | ID: wpr-7857
ABSTRACT
We report a case of IgA kappa light chain deposition disease and combined adult Fanconi syndrome with Auer rod-like intracytoplasmic inclusions in plasma cells and proximal renal tubular cells in a 54-yr-old female. Cytochemical stainings revealed a strong acid phosphatase activity of the inclusions and weak periodic acid-Schiff positivity, whereas the reactions for peroxidase and alpha-naphthyl acetate esterase were negative. An immunostaining verified IgA-kappa inside the plasma cells. Kidney biopsy revealed Bence Jones cast nephropathy with kappa light chain positivity, and Congo red staining was negative. Electron microscopy showed needle-shaped crystals located in tubular epithelial cells.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Paraproteinemias / Plasma Cells / Immunoglobulin A / Inclusion Bodies / Immunoglobulin kappa-Chains / Fanconi Syndrome / Kidney Tubules, Proximal Limits: Female / Humans Language: Korean Journal: The Korean Journal of Laboratory Medicine Year: 2007 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Paraproteinemias / Plasma Cells / Immunoglobulin A / Inclusion Bodies / Immunoglobulin kappa-Chains / Fanconi Syndrome / Kidney Tubules, Proximal Limits: Female / Humans Language: Korean Journal: The Korean Journal of Laboratory Medicine Year: 2007 Type: Article