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A case presentation of renal involvement in MCTD / 대한내과학회지
Korean Journal of Medicine ; : 457-462, 2005.
Artículo en Coreano | WPRIM | ID: wpr-156961
ABSTRACT
MCTD (Mixed Connective Tissue Disease) is a rare disease characterized by clinical characteristics of patients with overlapping features of SLE (systemic lupus erythematosus), SS (systemic sclerosis), and PM (polymyositis), and serologically characterized by high titers of Anti U1 RNP Ab. At early stage, finger swelling or Raynaud's phenomenon with high titers of Anti U1 RNP Ab are only apparent. Proteinuria and membranous nephropathy are characteristic renal manifestation of MCTD. Recently we had the opportunity to observe patient with Raynaud's phenomenon, finger swelling, high titers of Anti U1 RNP Ab, and asymptomatic proteinuria who underwent a renal biopsy. The patient was diagnosed as early MCTD and renal histology revealed membranous nephropathy. Our purpose is to report this patient and to review the literature.
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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Proteinuria / Biopsia / Glomerulonefritis Membranosa / Tejido Conectivo / Enfermedades Raras / Dedos / Enfermedad Mixta del Tejido Conjuntivo Límite: Humanos Idioma: Coreano Revista: Korean Journal of Medicine Año: 2005 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Proteinuria / Biopsia / Glomerulonefritis Membranosa / Tejido Conectivo / Enfermedades Raras / Dedos / Enfermedad Mixta del Tejido Conjuntivo Límite: Humanos Idioma: Coreano Revista: Korean Journal of Medicine Año: 2005 Tipo del documento: Artículo