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  • Title: [Acquired renal cystic disease. Polysyndromatic entity as cause of non-immunological progression of renal failure].
    Author: Nadal MA, De Rosa M, López Blanco OA, Cavalli NH, Iotti RM, Gotlieb D.
    Journal: Medicina (B Aires); 1999; 59(6):763-6. PubMed ID: 10752223.
    Abstract:
    We present a patient with rapidly progressive glomerulonephritis who after immunosuppression and hemodialysis treatment showed an improvement in his condition. Eight years later a computed tomography discovered an acquired renal cystic disease (ARCD) characterized by the development of 3 or more cysts in both kidneys of patients with chronic renal disorders and no history of hereditary cystic disease. ARCD may be asymptomatic or as it occurred in this patient, associated with several complications related to renal cysts such as polyuria-polydipsia syndrome, renal hemorrhagic cyst, perinephric hemorrhage and renal cell carcinoma. Along 12 years of follow-up the renal function showed a very slow declination which could be attributed to ARCD. It is suggested that ARCD can be considered as a non-immunological factor of renal progression when it develops in patients with mild chronic renal failure.
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