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.
| Original language | English |
|---|---|
| Pages (from-to) | 1665-1668 |
| Number of pages | 4 |
| Journal | Journal of Ultrasound in Medicine |
| Volume | 39 |
| Issue number | 8 |
| DOIs | |
| State | Published - 1 Aug 2020 |
Keywords
- congenital anomalies of the kidney and urinary tract, Mayer-Rokitansky-Küster-Hauser syndrome
- pancake kidney
- prenatal diagnosis
- prenatal ultrasound
All Science Journal Classification (ASJC) codes
- Radiological and Ultrasound Technology
- Radiology Nuclear Medicine and imaging
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