Your browser doesn't support javascript.
loading
Complete Remission from C1q Nephropathy with Disappearance of C1q Deposition after Steroid Therapy / 대한내과학회지
Korean Journal of Medicine ; : 311-315, 2016.
Article in En | WPRIM | ID: wpr-20326
Responsible library: WPRO
ABSTRACT
C1q nephropathy is a rare glomerular disease, defined by characteristic mesangial C1q immune deposition seen in immunofluorescence microscopy with no serological evidence of systemic lupus erythematosus. C1q nephropathy can be diagnosed with a subsequent biopsy, as with IgA nephropathy. There are some cases with an initial diagnosis of hematuria and proteinuria with minimal disease changes, focal segmental glomerulonephritis, and mesangial proliferative glomerulonephritis, but lacking C1q nephropathy, in which C1q deposition on immunofluorescence subsequently develops. We report a case that was diagnosed as diffuse mesangial proliferative glomerulonephritis, but a subsequent biopsy showed C1q nephropathy, with C1q deposition in both immunohistochemistry and electron microscopy (EM). We treated the C1q nephropathy with methylprednisolone and confirmed the disappearance of C1q depositions by both immunohistochemistry and EM in a follow-up biopsy.
Subject(s)
Key words
Full text: 1 Index: WPRIM Main subject: Proteinuria / Biopsy / Methylprednisolone / Immunohistochemistry / Microscopy, Electron / Complement C1q / Follow-Up Studies / Fluorescent Antibody Technique / Diagnosis / Glomerulonephritis Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies Language: En Journal: Korean Journal of Medicine Year: 2016 Type: Article
Full text: 1 Index: WPRIM Main subject: Proteinuria / Biopsy / Methylprednisolone / Immunohistochemistry / Microscopy, Electron / Complement C1q / Follow-Up Studies / Fluorescent Antibody Technique / Diagnosis / Glomerulonephritis Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies Language: En Journal: Korean Journal of Medicine Year: 2016 Type: Article