JUM Parker Laboratories, Inc
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sepulveda, W.
Right arrow Articles by Castro, V.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sepulveda, W.
Right arrow Articles by Castro, V.
© 2005 by the American Institute of Ultrasound in Medicine
J Ultrasound Med 24:1303-1308 • 0278-4297


Case Series

Congenital Megalourethra

Outcome After Prenatal Diagnosis in a Series of 4 Cases

Waldo Sepulveda, MD, Carlos Elorza, MD, Jorge Gutierrez, MD, Patricio Vasquez, MD and Victor Castro, MD

Fetal Medicine Center, Department of Obstetrics and Gynecology, Clinica Las Condes, Santiago, Chile (W.S.); Fetal Medicine Unit, San Jose Hospital, University of Santiago de Chile, Santiago, Chile (W.S., J.G., P.V.); Department of Urology, Roberto del Rio Hospital, Santiago, Chile (V.C.); and Ultrasound Unit, Department of Diagnostic Imaging, Universidad Nacional, Rosario, Argentina (C.E.).

Address correspondence to Waldo Sepulveda, MD, Fetal Medicine Center, Clinica Las Condes, Casilla 208, Santiago 20, Chile. E-mail: fetalmed{at}yahoo.com

Objective. The purpose of this series is to describe the prenatal sonographic findings and pregnancy outcome in 4 cases of congenital megalourethra. Methods. Three cases of fusiform-type megalourethra and 1 case of scaphoid-type megalourethtra were diagnosed prenatally by sonography between 20 and 24 weeks’ gestation. The key findings for diagnosis included sonographic features of lower urinary tract obstruction in association with dilatation and elongation of the penile urethra in all 4 cases. Severe oligohydramnios was detected at the time of diagnosis in only 1 case. Prenatal chromosome analysis was available in 3 cases and revealed a normal 46,XY karyotype. Information on pregnancy outcome was available in all cases. Results. The parents opted for elective termination of pregnancy in 1 case when decreased amniotic fluid volume and echogenic kidneys were documented at the follow-up scan. Among the 3 ongoing pregnancies, there were 2 premature cesarean deliveries at 28 and 31 weeks and 1 vaginal delivery at term. All neonates had severe lung hypoplasia and died in the early neonatal period. Conclusions. Congenital megalourethra is associated with poor perinatal outcome. Because this condition can be diagnosed prenatally in the context of lower urinary tract obstruction, detailed examination of the external genitalia in these cases should be mandatory.

Key Words: fetal anomalies • megalourethra • prenatal diagnosis • prenatal sonography




This article has been cited by other articles:


Home page
J Ultrasound MedHome page
J. R. Wax, M. G. Pinette, A. Landes, A. Cartin, and J. Blackstone
Prenatal Sonographic Diagnosis of Congenital Megalourethra With In Utero Spontaneous Resolution
J. Ultrasound Med., October 1, 2009; 28(10): 1385 - 1388.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2005 by the American Institute of Ultrasound in Medicine.