Daño hepatocelular, proteinuria y autoinmunidad: ¿enfermedad multisistémica o coincidencia de enfermedades? Caso Clínico
Palabras clave:
Glomerulosclerosis, Focal Segmental, Hepatitis, Autoimmune, ProteinuriaResumen
We report a 19 years old male presenting with knee pain, elevated liver enzymes and proteinuria. Further investigation found positive antinuclear and anti-smooth muscle antibodies and a liver biopsy revealed the presence of an autoimmune hepatitis. Treatment with corticosteroids and azathioprine was started, resulting in normalization of liver enzymes but proteinuria persisted and a kidney biopsy disclosed a focal segmental glomerulosclerosis. The use of lisinopril resulted in a significative reduction of proteinuria and, after 30 months of follow up, he continues with azathioprine, lisinopril and a low prednisone dose without evidence of liver or kidney disease activity.Descargas
Publicado
2018-07-04
Cómo citar
Herrera, P., Ruiz, A., Carpio, D., & Ardiles, L. (2018). Daño hepatocelular, proteinuria y autoinmunidad: ¿enfermedad multisistémica o coincidencia de enfermedades? Caso Clínico. Revista Médica De Chile, 146(6). Recuperado a partir de https://mail.revistamedicadechile.cl/index.php/rmedica/article/view/6563
Número
Sección
Reporte de Caso Clínico