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Successful surgical treatment of omphalocele with umbilical evagination of the bladder: an extremely rare presentation of neonatal case
BACKGROUND: A few cases of small omphalocele with umbilical evagination of the bladder have been reported. However, its embryology is yet to be elucidated. Only a few reports have indicated the existence of urachal anomalies and umbilical cysts related to bladder evagination. The incidence of uracha...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10333145/ https://www.ncbi.nlm.nih.gov/pubmed/37428342 http://dx.doi.org/10.1186/s40792-023-01710-y |
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author | Kobayashi, Haruka Baba, Tokuro Kuda, Masaaki Ieiri, Satoshi Takatsuki, Mitsuhisa |
author_facet | Kobayashi, Haruka Baba, Tokuro Kuda, Masaaki Ieiri, Satoshi Takatsuki, Mitsuhisa |
author_sort | Kobayashi, Haruka |
collection | PubMed |
description | BACKGROUND: A few cases of small omphalocele with umbilical evagination of the bladder have been reported. However, its embryology is yet to be elucidated. Only a few reports have indicated the existence of urachal anomalies and umbilical cysts related to bladder evagination. The incidence of urachal anomalies at birth is reported to be 1 in 5000–8000 live birth, and urachal aplasia is rare. Herein, we report a rare, novel case of urachal aplasia. CASE PRESENTATION: We encountered a small omphalocele with bladder evagination associated with urachal aplasia for which the neonate underwent surgery one day after birth. The patient was a one-day-old boy with a prenatally diagnosed omphalocele. A fetal magnetic resonance image (MRI) scan (25 weeks of gestation) revealed a 30 × 33 mm (approximately 1.3 in.) cystic lesion which was suspected to be an umbilical cyst. The baby was born vaginally at 38 weeks, weighing 2956 g. An omphalocele (hernial orifice diameter, 4 cm × 3 cm) with bladder prolapse was recognized. After sac excision, the prolapsed bladder was resected and closed with two-layer sutures. In order to secure sufficient bladder capacity, we estimated the minimum residual volume as 21 ml after bladder plasty. The remaining bladder capacity was confirmed to be 30 ml by injecting a contrast dye and saline into the bladder. The neonate had no associated cardiac urogenital or skeletal anomalies. Postoperative course was uneventful. The patient was regularly followed up for two years after surgery and underwent umbilicoplasty. He had no trouble with urinary function. CONCLUSION: In this case, we experienced extremely rare condition of a small omphalocele with bladder evagination associated with urachal aplasia and reviewed 7 case reports of anomalies similar to those in the present case. Umbilical cord cysts may be an informative indicator of these symptoms in utero. Therefore, ultrasonography scans should be conducted until delivery, despite the spontaneous disappearance of cord cysts. |
format | Online Article Text |
id | pubmed-10333145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-103331452023-07-12 Successful surgical treatment of omphalocele with umbilical evagination of the bladder: an extremely rare presentation of neonatal case Kobayashi, Haruka Baba, Tokuro Kuda, Masaaki Ieiri, Satoshi Takatsuki, Mitsuhisa Surg Case Rep Case Report BACKGROUND: A few cases of small omphalocele with umbilical evagination of the bladder have been reported. However, its embryology is yet to be elucidated. Only a few reports have indicated the existence of urachal anomalies and umbilical cysts related to bladder evagination. The incidence of urachal anomalies at birth is reported to be 1 in 5000–8000 live birth, and urachal aplasia is rare. Herein, we report a rare, novel case of urachal aplasia. CASE PRESENTATION: We encountered a small omphalocele with bladder evagination associated with urachal aplasia for which the neonate underwent surgery one day after birth. The patient was a one-day-old boy with a prenatally diagnosed omphalocele. A fetal magnetic resonance image (MRI) scan (25 weeks of gestation) revealed a 30 × 33 mm (approximately 1.3 in.) cystic lesion which was suspected to be an umbilical cyst. The baby was born vaginally at 38 weeks, weighing 2956 g. An omphalocele (hernial orifice diameter, 4 cm × 3 cm) with bladder prolapse was recognized. After sac excision, the prolapsed bladder was resected and closed with two-layer sutures. In order to secure sufficient bladder capacity, we estimated the minimum residual volume as 21 ml after bladder plasty. The remaining bladder capacity was confirmed to be 30 ml by injecting a contrast dye and saline into the bladder. The neonate had no associated cardiac urogenital or skeletal anomalies. Postoperative course was uneventful. The patient was regularly followed up for two years after surgery and underwent umbilicoplasty. He had no trouble with urinary function. CONCLUSION: In this case, we experienced extremely rare condition of a small omphalocele with bladder evagination associated with urachal aplasia and reviewed 7 case reports of anomalies similar to those in the present case. Umbilical cord cysts may be an informative indicator of these symptoms in utero. Therefore, ultrasonography scans should be conducted until delivery, despite the spontaneous disappearance of cord cysts. Springer Berlin Heidelberg 2023-07-10 /pmc/articles/PMC10333145/ /pubmed/37428342 http://dx.doi.org/10.1186/s40792-023-01710-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Case Report Kobayashi, Haruka Baba, Tokuro Kuda, Masaaki Ieiri, Satoshi Takatsuki, Mitsuhisa Successful surgical treatment of omphalocele with umbilical evagination of the bladder: an extremely rare presentation of neonatal case |
title | Successful surgical treatment of omphalocele with umbilical evagination of the bladder: an extremely rare presentation of neonatal case |
title_full | Successful surgical treatment of omphalocele with umbilical evagination of the bladder: an extremely rare presentation of neonatal case |
title_fullStr | Successful surgical treatment of omphalocele with umbilical evagination of the bladder: an extremely rare presentation of neonatal case |
title_full_unstemmed | Successful surgical treatment of omphalocele with umbilical evagination of the bladder: an extremely rare presentation of neonatal case |
title_short | Successful surgical treatment of omphalocele with umbilical evagination of the bladder: an extremely rare presentation of neonatal case |
title_sort | successful surgical treatment of omphalocele with umbilical evagination of the bladder: an extremely rare presentation of neonatal case |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10333145/ https://www.ncbi.nlm.nih.gov/pubmed/37428342 http://dx.doi.org/10.1186/s40792-023-01710-y |
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