Fetal Pancake Kidney: Prenatal Diagnosis and Postnatal Follow-up

J Ultrasound Med. 2020 Aug;39(8):1665-1668. doi: 10.1002/jum.15251. Epub 2020 Feb 27.

Abstract

Bilateral failure of the kidneys to ascend during embryonic life may lead to fusion of the two renal masses, resulting in a round mass known as pancake kidney. Reviewing the literature, we did not encounter any reports of prenatal diagnosis of pancake kidneys. We present 6 cases of a pancake kidney diagnosed prenatally. Extrarenal associated anomalies included an aberrant right subclavian artery, nonvisualization of the uterus, consistent with Mayer-Rokitansky-Küster-Hauser syndrome, and a sequence of early-onset growth restriction, hypospadias, and syndactyly, suspected as Smith-Lemli-Opitz syndrome. On postnatal follow-up, all infants had a normal renal outcome.

Keywords: congenital anomalies of the kidney and urinary tract, Mayer-Rokitansky-Küster-Hauser syndrome; pancake kidney; prenatal diagnosis; prenatal ultrasound.

Publication types

  • Case Reports

MeSH terms

  • 46, XX Disorders of Sex Development*
  • Congenital Abnormalities* / diagnostic imaging
  • Female
  • Follow-Up Studies
  • Humans
  • Infant
  • Kidney / diagnostic imaging
  • Male
  • Mullerian Ducts
  • Pregnancy
  • Prenatal Diagnosis
  • Vagina