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Prenatal diagnosis of congenital megalourethra in the second trimester of pregnancy

Congenital megalourethra is abnormal dilation of the penile urethra due to aplasia of erectile tissue, leading to lower urinary tract obstruction. This condition should be considered when fetal penis with typical dilation is seen on prenatal scan. The dilated structure, however, can be easily missed...

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Autores principales: Anh, Do Duy, Nguyen, Ha To, Meagher, Simon, Júnior, Edward Araujo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Exeley Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988452/
https://www.ncbi.nlm.nih.gov/pubmed/32021712
http://dx.doi.org/10.15557/JoU.2019.0045
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author Anh, Do Duy
Nguyen, Ha To
Meagher, Simon
Júnior, Edward Araujo
author_facet Anh, Do Duy
Nguyen, Ha To
Meagher, Simon
Júnior, Edward Araujo
author_sort Anh, Do Duy
collection PubMed
description Congenital megalourethra is abnormal dilation of the penile urethra due to aplasia of erectile tissue, leading to lower urinary tract obstruction. This condition should be considered when fetal penis with typical dilation is seen on prenatal scan. The dilated structure, however, can be easily missed or misinterpreted as the umbilical cord. Perinatal prognosis is poor due to direct consequences on urinary and respiratory systems, or due to severe associated anomalies. A large number of survived cases experience urinary sequelae and renal impairment. We report one case of fetal congenital megalourethra diagnosed at 17 weeks and 6 days of pregnancy.
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spelling pubmed-69884522020-02-04 Prenatal diagnosis of congenital megalourethra in the second trimester of pregnancy Anh, Do Duy Nguyen, Ha To Meagher, Simon Júnior, Edward Araujo J Ultrason Medicine Congenital megalourethra is abnormal dilation of the penile urethra due to aplasia of erectile tissue, leading to lower urinary tract obstruction. This condition should be considered when fetal penis with typical dilation is seen on prenatal scan. The dilated structure, however, can be easily missed or misinterpreted as the umbilical cord. Perinatal prognosis is poor due to direct consequences on urinary and respiratory systems, or due to severe associated anomalies. A large number of survived cases experience urinary sequelae and renal impairment. We report one case of fetal congenital megalourethra diagnosed at 17 weeks and 6 days of pregnancy. Exeley Inc. 2019-12 2019-12-31 /pmc/articles/PMC6988452/ /pubmed/32021712 http://dx.doi.org/10.15557/JoU.2019.0045 Text en © Polish Ultrasound Society http://creativecommons.org/licenses/cc-by-nc-nd/4.0/ http://creativecommons.org/licenses/cc-by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial NoDerivatives License (CC BY-NC-ND). Reproduction is permitted for personal, educational, non-commercial use, provided that the original article is in whole, unmodified, and properly cited.
spellingShingle Medicine
Anh, Do Duy
Nguyen, Ha To
Meagher, Simon
Júnior, Edward Araujo
Prenatal diagnosis of congenital megalourethra in the second trimester of pregnancy
title Prenatal diagnosis of congenital megalourethra in the second trimester of pregnancy
title_full Prenatal diagnosis of congenital megalourethra in the second trimester of pregnancy
title_fullStr Prenatal diagnosis of congenital megalourethra in the second trimester of pregnancy
title_full_unstemmed Prenatal diagnosis of congenital megalourethra in the second trimester of pregnancy
title_short Prenatal diagnosis of congenital megalourethra in the second trimester of pregnancy
title_sort prenatal diagnosis of congenital megalourethra in the second trimester of pregnancy
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6988452/
https://www.ncbi.nlm.nih.gov/pubmed/32021712
http://dx.doi.org/10.15557/JoU.2019.0045
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