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Case Report: Pre- and postnatal management of an allantoic cyst with patent urachus and single umbilical artery
Patent urachus is a rare congenital abnormality. Since its first description by Cabriolus in 1550, few cases have been reported. A 26-year-old Vietnamese primigravida presented at 20 weeks of gestation for evaluation of a cystic mass in the umbilical cord, which was first discovered at week 13 of pr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505787/ https://www.ncbi.nlm.nih.gov/pubmed/26213613 http://dx.doi.org/10.12688/f1000research.6546.1 |
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author | Trong Thach, Than Duy Quan, Vo Diem Nghi, Tran Hoang Anh, Nguyen Phi Hung, Le Thien Luan, Nguyen Phuoc Long, Nguyen |
author_facet | Trong Thach, Than Duy Quan, Vo Diem Nghi, Tran Hoang Anh, Nguyen Phi Hung, Le Thien Luan, Nguyen Phuoc Long, Nguyen |
author_sort | Trong Thach, Than |
collection | PubMed |
description | Patent urachus is a rare congenital abnormality. Since its first description by Cabriolus in 1550, few cases have been reported. A 26-year-old Vietnamese primigravida presented at 20 weeks of gestation for evaluation of a cystic mass in the umbilical cord, which was first discovered at week 13 of pregnancy by ultrasound scan. The cystic mass originated from the root of the umbilical cord, connected to the urinary bladder, and no intestinal contents were enclosed within. Doppler ultrasound assessment showed that the single umbilical artery existed within the normal range. The progression of the umbilical cyst continued to be screened, but the mass disappeared on ultrasound images at 27 weeks of gestation. This led to the consideration of the cyst’s rupture. After 38 gestational weeks, the pregnant woman delivered a 3350g male infant via cesarean section because of an obstructed vaginal labor. The following days, a stream of urine was recorded leaking out from the umbilical mass whenever he cried. Seven weeks after delivery, an open surgical approach was successfully performed. The baby is now 43 months of age, growing and developing normally. Since an allantoic cyst with patent urachus is a rare clinical entity, early discovery, close monitoring and accurate diagnosis through ultrasound in the prenatal period may consequently allow clinicians to have suitable attitudes towards management when the infant is born. |
format | Online Article Text |
id | pubmed-4505787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-45057872015-07-24 Case Report: Pre- and postnatal management of an allantoic cyst with patent urachus and single umbilical artery Trong Thach, Than Duy Quan, Vo Diem Nghi, Tran Hoang Anh, Nguyen Phi Hung, Le Thien Luan, Nguyen Phuoc Long, Nguyen F1000Res Case Report Patent urachus is a rare congenital abnormality. Since its first description by Cabriolus in 1550, few cases have been reported. A 26-year-old Vietnamese primigravida presented at 20 weeks of gestation for evaluation of a cystic mass in the umbilical cord, which was first discovered at week 13 of pregnancy by ultrasound scan. The cystic mass originated from the root of the umbilical cord, connected to the urinary bladder, and no intestinal contents were enclosed within. Doppler ultrasound assessment showed that the single umbilical artery existed within the normal range. The progression of the umbilical cyst continued to be screened, but the mass disappeared on ultrasound images at 27 weeks of gestation. This led to the consideration of the cyst’s rupture. After 38 gestational weeks, the pregnant woman delivered a 3350g male infant via cesarean section because of an obstructed vaginal labor. The following days, a stream of urine was recorded leaking out from the umbilical mass whenever he cried. Seven weeks after delivery, an open surgical approach was successfully performed. The baby is now 43 months of age, growing and developing normally. Since an allantoic cyst with patent urachus is a rare clinical entity, early discovery, close monitoring and accurate diagnosis through ultrasound in the prenatal period may consequently allow clinicians to have suitable attitudes towards management when the infant is born. F1000Research 2015-05-22 /pmc/articles/PMC4505787/ /pubmed/26213613 http://dx.doi.org/10.12688/f1000research.6546.1 Text en Copyright: © 2015 Trong Thach T et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/publicdomain/zero/1.0/ Data associated with the article are available under the terms of the Creative Commons Zero "No rights reserved" data waiver (CC0 1.0 Public domain dedication). |
spellingShingle | Case Report Trong Thach, Than Duy Quan, Vo Diem Nghi, Tran Hoang Anh, Nguyen Phi Hung, Le Thien Luan, Nguyen Phuoc Long, Nguyen Case Report: Pre- and postnatal management of an allantoic cyst with patent urachus and single umbilical artery |
title | Case Report: Pre- and postnatal management of an allantoic cyst with patent urachus and single umbilical artery |
title_full | Case Report: Pre- and postnatal management of an allantoic cyst with patent urachus and single umbilical artery |
title_fullStr | Case Report: Pre- and postnatal management of an allantoic cyst with patent urachus and single umbilical artery |
title_full_unstemmed | Case Report: Pre- and postnatal management of an allantoic cyst with patent urachus and single umbilical artery |
title_short | Case Report: Pre- and postnatal management of an allantoic cyst with patent urachus and single umbilical artery |
title_sort | case report: pre- and postnatal management of an allantoic cyst with patent urachus and single umbilical artery |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505787/ https://www.ncbi.nlm.nih.gov/pubmed/26213613 http://dx.doi.org/10.12688/f1000research.6546.1 |
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