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Unusual fetal ascites and spontaneous bladder rupture in a female fetus: a case report

BACKGROUND: Fetal bladder rupture causing urinary ascites is uncommon. It is generally related to invasive fetal medicine procedures or obstructive disorders such as in posterior urethral valves in male fetuses. An exceptional case of spontaneous bladder rupture in a female fetus occurred in a pregn...

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Autores principales: Cadoret, Florence, Brazet, Edith, Sartor, Agnès, Lacroix, Isabelle, Casper, Charlotte, Decramer, Stéphane, Parant, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7370489/
https://www.ncbi.nlm.nih.gov/pubmed/32684161
http://dx.doi.org/10.1186/s13256-020-02425-6
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author Cadoret, Florence
Brazet, Edith
Sartor, Agnès
Lacroix, Isabelle
Casper, Charlotte
Decramer, Stéphane
Parant, Olivier
author_facet Cadoret, Florence
Brazet, Edith
Sartor, Agnès
Lacroix, Isabelle
Casper, Charlotte
Decramer, Stéphane
Parant, Olivier
author_sort Cadoret, Florence
collection PubMed
description BACKGROUND: Fetal bladder rupture causing urinary ascites is uncommon. It is generally related to invasive fetal medicine procedures or obstructive disorders such as in posterior urethral valves in male fetuses. An exceptional case of spontaneous bladder rupture in a female fetus occurred in a pregnant woman treated with high doses of opiates in an intensive care unit. This unusual obstetric situation leads to discussion of the possible causes of fetal bladder rupture, its management, and the pediatric prognosis. CASE PRESENTATION: We report the case of a 30-year-old nulliparous black woman with a history of mesenteric cystic lymphangioma and multiple bowel resections leading to chronic malabsorption. During her pregnancy, our patient presented with an occlusive syndrome and major bilateral renal dilation. Urinary derivation resulted in iatrogenic bilateral ureteral perforation. Our patient thus presented with major uroperitoneum, bilateral pleural effusion and acute renal failure, treated by thoracic drainage and bilateral nephrostomy. Postoperative pain required treatment with level III analgesics. In this context, 5 days after morphine treatment introduction an enlarged fetal bladder was observed, followed 3 days later by voluminous fetal ascites. The diagnosis of spontaneous bladder rupture was suspected. After multidisciplinary discussion, expectant management was decided. At 31 weeks and 4 days gestation, our patient went into spontaneous labor with a subsequent vaginal delivery. The infant required resuscitation and paracentesis of ascites at birth. Her neonatal course was favorable with a simple urethral bladder drainage. Cystography at day 9 was normal. At 2 years of follow-up, the mother and the child have a normal course. CONCLUSIONS: An iatrogenic origin of megacystis in a female fetus must be evoked in the event of maternal administration of high doses of opiates in the second part of her pregnancy. In our case, the megacystis was followed by spontaneous bladder rupture at 30 weeks of gestation, with a favorable maternal fetal issue.
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spelling pubmed-73704892020-07-21 Unusual fetal ascites and spontaneous bladder rupture in a female fetus: a case report Cadoret, Florence Brazet, Edith Sartor, Agnès Lacroix, Isabelle Casper, Charlotte Decramer, Stéphane Parant, Olivier J Med Case Rep Case Report BACKGROUND: Fetal bladder rupture causing urinary ascites is uncommon. It is generally related to invasive fetal medicine procedures or obstructive disorders such as in posterior urethral valves in male fetuses. An exceptional case of spontaneous bladder rupture in a female fetus occurred in a pregnant woman treated with high doses of opiates in an intensive care unit. This unusual obstetric situation leads to discussion of the possible causes of fetal bladder rupture, its management, and the pediatric prognosis. CASE PRESENTATION: We report the case of a 30-year-old nulliparous black woman with a history of mesenteric cystic lymphangioma and multiple bowel resections leading to chronic malabsorption. During her pregnancy, our patient presented with an occlusive syndrome and major bilateral renal dilation. Urinary derivation resulted in iatrogenic bilateral ureteral perforation. Our patient thus presented with major uroperitoneum, bilateral pleural effusion and acute renal failure, treated by thoracic drainage and bilateral nephrostomy. Postoperative pain required treatment with level III analgesics. In this context, 5 days after morphine treatment introduction an enlarged fetal bladder was observed, followed 3 days later by voluminous fetal ascites. The diagnosis of spontaneous bladder rupture was suspected. After multidisciplinary discussion, expectant management was decided. At 31 weeks and 4 days gestation, our patient went into spontaneous labor with a subsequent vaginal delivery. The infant required resuscitation and paracentesis of ascites at birth. Her neonatal course was favorable with a simple urethral bladder drainage. Cystography at day 9 was normal. At 2 years of follow-up, the mother and the child have a normal course. CONCLUSIONS: An iatrogenic origin of megacystis in a female fetus must be evoked in the event of maternal administration of high doses of opiates in the second part of her pregnancy. In our case, the megacystis was followed by spontaneous bladder rupture at 30 weeks of gestation, with a favorable maternal fetal issue. BioMed Central 2020-07-19 /pmc/articles/PMC7370489/ /pubmed/32684161 http://dx.doi.org/10.1186/s13256-020-02425-6 Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Cadoret, Florence
Brazet, Edith
Sartor, Agnès
Lacroix, Isabelle
Casper, Charlotte
Decramer, Stéphane
Parant, Olivier
Unusual fetal ascites and spontaneous bladder rupture in a female fetus: a case report
title Unusual fetal ascites and spontaneous bladder rupture in a female fetus: a case report
title_full Unusual fetal ascites and spontaneous bladder rupture in a female fetus: a case report
title_fullStr Unusual fetal ascites and spontaneous bladder rupture in a female fetus: a case report
title_full_unstemmed Unusual fetal ascites and spontaneous bladder rupture in a female fetus: a case report
title_short Unusual fetal ascites and spontaneous bladder rupture in a female fetus: a case report
title_sort unusual fetal ascites and spontaneous bladder rupture in a female fetus: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7370489/
https://www.ncbi.nlm.nih.gov/pubmed/32684161
http://dx.doi.org/10.1186/s13256-020-02425-6
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