• Media type: E-Article
  • Title: Antenatal Diagnostic Aspects of Unilateral Multicystic Kidney Dysplasia – Sensitivity, Specificity, Predictive Values, Differential Diagnoses, Associated Malformations and Consequences
  • Contributor: Eckoldt, Felicitas; Woderich, R.; Smith, R.D.; Heling, K.-S.
  • Published: S. Karger AG, 2004
  • Published in: Fetal Diagnosis and Therapy, 19 (2004) 2, Seite 163-169
  • Language: English
  • DOI: 10.1159/000075143
  • ISSN: 1015-3837; 1421-9964
  • Origination:
  • Footnote:
  • Description: <i>Objectives:</i> Unilateral multicystic kidney dysplasia (MCKD) is the second most common urinary tract abnormality diagnosed antenatally. Whilst an isolated unilateral MCKD has a good prognosis, a poor outcome must be expected when MCKD is associated with other complex abnormalities. <i>Material:</i> Out of 11,176 cases, 693 fetuses were suspected of having urinary tract abnormalities. Urological findings were confirmed in 548 of them. Unilateral cystic kidney was diagnosed prenatally in 85 cases. <i>Results:</i> The study results in a total of 107 cases with proven MCKD. Eighty-five pregnancies with a prenatal diagnosis of MCKD were analysed. The antenatal diagnosis of MCKD was confirmed in 56 cases. Fifty-one children were found to have unilateral MCKD where this had not been explicitly suspected from antenatal scanning. <i>Conclusion:</i> Unilateral MCKD is a malformation with an excellent prognosis for child survival and global renal function if encountered in isolation. However, our analysis of live infants and autopsy cases demonstrates a high proportion of severe associated malformations of the urinary tract and other organ systems.