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.
Artigo em Inglês | WPRIM | ID: wpr-20326
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.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Proteinúria / Biópsia / Metilprednisolona / Imuno-Histoquímica / Microscopia Eletrônica / Complemento C1q / Seguimentos / Imunofluorescência / Diagnóstico / Glomerulonefrite Tipo de estudo: Estudo diagnóstico / Estudo observacional / Estudo prognóstico Idioma: Inglês Revista: Korean Journal of Medicine Ano de publicação: 2016 Tipo de documento: Artigo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Proteinúria / Biópsia / Metilprednisolona / Imuno-Histoquímica / Microscopia Eletrônica / Complemento C1q / Seguimentos / Imunofluorescência / Diagnóstico / Glomerulonefrite Tipo de estudo: Estudo diagnóstico / Estudo observacional / Estudo prognóstico Idioma: Inglês Revista: Korean Journal of Medicine Ano de publicação: 2016 Tipo de documento: Artigo