Anterior Urethral Valve: Uncommon Association with Renal Duplicity

Authors

  • Amina Ben Salem University of Monastir
  • Ines Mazhoud
  • Rachida Laamiri
  • Randa Salem University of Monastir
  • Hayet Laajili University of Monastir
  • Chiraz Hafsa University of Monastir

DOI:

https://doi.org/10.21699/jns.v6i2.544

Keywords:

Anterior urethral valve, Prenatal diagnosis, Fetus, Duplex kidney

Abstract

Anterior urethral valves (AUVs) is an unusual cause of congenital obstruction of the male urethra, being 15–30 times less common than posterior urethral valves. We present a case of AUV diagnosed at 24th gestational week. Ultrasonography and fetal MRI revealed hydronephrotic kidneys with ureteral duplicity, a distended bladder and perineal cystic mass which confirmed dilated anterior urethra in a male fetus. Diagnosis was confirmed postnatally by voiding cystourethrogram and surgery.

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Published

2017-04-15

How to Cite

1.
Ben Salem A, Mazhoud I, Laamiri R, Salem R, Laajili H, Hafsa C. Anterior Urethral Valve: Uncommon Association with Renal Duplicity. J Neonatal Surg [Internet]. 2017Apr.15 [cited 2024Apr.18];6(2):41. Available from: https://www.jneonatalsurg.com/ojs/index.php/jns/article/view/496

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