Congenital megacalycosis with IgA nephropathy: a case report and review of the literature

Ren Fail. 2013;35(1):155-8. doi: 10.3109/0886022X.2012.731996. Epub 2012 Dec 20.

Abstract

Congenital megacalycosis is a rare renal disease characterized by calyceal dilatation without pelvic or ureteral obstruction. If not accompanied by nephrolithiasis and urinary tract infection, this disease is completely benign and does not cause renal dysfunction. We present a case of congenital megacalycosis that was diagnosed at the age of 41 (oldest case in the literature) after admitting with hematuria and acute renal dysfunction. IgA nephropathy was also diagnosed in this patient. Since renal dysfunction is not likely in these patients, if encountered; renal biopsy should be performed although technically difficult to diagnose the cause of this dysfunction.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Biopsy
  • Diagnosis, Differential
  • Glomerulonephritis, IGA / complications*
  • Glomerulonephritis, IGA / diagnosis
  • Hematuria
  • Humans
  • Kidney / pathology*
  • Kidney Diseases / complications
  • Kidney Diseases / congenital*
  • Kidney Diseases / diagnosis
  • Magnetic Resonance Imaging*
  • Male
  • Urography / methods*