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Membranous Nephropathy Relapsed after 20-year of Complete Remission / 대한내과학회지
Korean Journal of Medicine ; : 295-299, 2017.
Artículo en Coreano | WPRIM | ID: wpr-189029
ABSTRACT
Membranous nephropathy is the most common pathologic lesion in adult patients with nephrotic syndrome. The cause is idiopathic, and the pathogenesis is believed to involve the deposition of immune complexes in the subepithelial tissue of the glomerular capillaries. After a period of 5 to 10 years, one-third of patients with membranous nephropathy will develop spontaneous remission, one-third will develop sustained proteinuria, and one-third will experience progression to chronic renal disease. Proteinuria may recur in patients who are in complete remission; this has been reported in approximately 26% of patients during an average of 89 months. To date, however, recurrence of membranous nephropathy has not been reported in patients who have been in complete remission for ≥ 20 years. We report herein such a case. Membranous nephropathy may recur in adult patients who are currently in the remission stage. Ongoing follow-up is therefore required, even after several years of complete remission.
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Proteinuria / Recurrencia / Remisión Espontánea / Capilares / Glomerulonefritis Membranosa / Estudios de Seguimiento / Insuficiencia Renal Crónica / Glomerulonefritis / Complejo Antígeno-Anticuerpo / Síndrome Nefrótico Tipo de estudio: Estudio observacional / Estudio pronóstico Límite: Adulto / Humanos Idioma: Coreano Revista: Korean Journal of Medicine Año: 2017 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Proteinuria / Recurrencia / Remisión Espontánea / Capilares / Glomerulonefritis Membranosa / Estudios de Seguimiento / Insuficiencia Renal Crónica / Glomerulonefritis / Complejo Antígeno-Anticuerpo / Síndrome Nefrótico Tipo de estudio: Estudio observacional / Estudio pronóstico Límite: Adulto / Humanos Idioma: Coreano Revista: Korean Journal of Medicine Año: 2017 Tipo del documento: Artículo