Document Type
Article
Publication Date
1-2020
Identifier
NBK557723
Abstract
atent urachus refers to one condition in a rare spectrum of disorders referred to as urachal anomalies. These conditions result from the failure of the involution of normal embryologic tissues that serve to empty the fetal bladder. The location and amount of persistent tissue dictate the presenting symptoms. Some of these urachal anomalies are obvious at birth, while others are more subtle and not diagnosed until adulthood or only incidentally discovered after imaging is obtained for other reasons. Historically, surgical resection of urachal anomalies was routinely undertaken, given the potential for malignancy in retained ectopic tissue. Early surgical resection has been challenged by many studies demonstrating not only the low incidence of the condition in general but the even lower chance of future malignancy. Accurate and expeditious diagnosis of urachal anomalies in the child with umbilical wetness, persistent drainage, recurrent urinary tract infections, and recurrent umbilical infections is required to assist with symptom relief, avoid recurrent severe infection, and to provide definitive treatment.
Journal Title
StatPearls
Recommended Citation
Briggs KB, Rentea RM. Patent Urachus. In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2020.
Included in
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Commons, Pediatrics Commons, Surgery Commons
Comments
Last updated: April 2020
NCBI BookShelf: https://www.ncbi.nlm.nih.gov/books/NBK557723/
This book is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits use, duplication, adaptation, distribution, and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, a link is provided to the Creative Commons license, and any changes made are indicated.