| Autor: |
Santos JE; Hospital Espírito Santo de Évora, Department of Nephrology, Évora, Portugal., Vicente R; Hospital Espírito Santo de Évora, Department of Nephrology, Évora, Portugal., Malvar B; Hospital Espírito Santo de Évora, Department of Nephrology, Évora, Portugal., Santos I; Hospital Espírito Santo de Évora, Department of Nephrology, Évora, Portugal., Coimbra M; Hospital Espírito Santo de Évora, Department of Nephrology, Évora, Portugal., Amoedo M; Hospital Espírito Santo de Évora, Department of Nephrology, Évora, Portugal., Pires C; Hospital Espírito Santo de Évora, Department of Nephrology, Évora, Portugal. |
| Abstrakt: |
Antineutrophil cytoplasmic antibodies (ANCAs) are associated with small vessel vasculitis but their prevalence is not rare in other immune diseases. In lupus nephritis (LN), their pathological role and clinical relevance have been the target of controversial views. We present a case of acute kidney injury and nephrotic syndrome in a young woman with diffuse global proliferative and membranous nephritis on her kidney biopsy, showing a full-house immunofluorescence pattern, very allusive of class IV + V LN, but lacking associated clinical criteria and laboratory findings to support the diagnosis of systemic lupus erythematosus (SLE). Furthermore, the patient presented with high titers of ANCA, steadily decreasing alongside the renal function and proteinuria improvements, with mycophenolate mofetil (MMF) and steroid treatment. The authors believe this is a case of lupus-like nephritis, in which ANCAs are immunological markers, although they are not directly involved in the pathogenesis. |
