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Spontaneous perirenal hemorrhage (Wunderlich syndrome) in the fetus: a case report
BACKGROUND: Spontaneous perirenal hemorrhage (Wunderlich syndrome) in the fetus is a rare urinary system disease. Prenatal ultrasound diagnosis presents challenges due to the lack of specific clinical features. CASE PRESENTATION: A 27-year-old Chinese woman gravida 2 para 0 found her fetus with the...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163762/ https://www.ncbi.nlm.nih.gov/pubmed/37147736 http://dx.doi.org/10.1186/s13256-023-03867-4 |
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author | Jia, Yongmei Gao, Junxia |
author_facet | Jia, Yongmei Gao, Junxia |
author_sort | Jia, Yongmei |
collection | PubMed |
description | BACKGROUND: Spontaneous perirenal hemorrhage (Wunderlich syndrome) in the fetus is a rare urinary system disease. Prenatal ultrasound diagnosis presents challenges due to the lack of specific clinical features. CASE PRESENTATION: A 27-year-old Chinese woman gravida 2 para 0 found her fetus with the left Wunderlich syndrome accompanying bilateral hydronephroses and bladder dysfunction with an early diagnosis through prenatal ultrasound and postnatal magnetic resonance imaging. After a timely emergency cesarean section, the infant was administrated antimicrobial prophylaxis and an indwelling catheter treatment. Ultrasound follow-up showed his urinary system gradually developed normally. CONCLUSION: A fetus with bilateral hydronephroses accompanying bladder dysfunction should be observed because of the risk of spontaneous renal rupture with hemorrhage formation. Ultrasound and magnetic resonance imaging play a vital role in the diagnosis and follow-up of Wunderlich syndrome. Early diagnosis facilitates better pregnancy planning and appropriate care of newborns. |
format | Online Article Text |
id | pubmed-10163762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101637622023-05-07 Spontaneous perirenal hemorrhage (Wunderlich syndrome) in the fetus: a case report Jia, Yongmei Gao, Junxia J Med Case Rep Case Report BACKGROUND: Spontaneous perirenal hemorrhage (Wunderlich syndrome) in the fetus is a rare urinary system disease. Prenatal ultrasound diagnosis presents challenges due to the lack of specific clinical features. CASE PRESENTATION: A 27-year-old Chinese woman gravida 2 para 0 found her fetus with the left Wunderlich syndrome accompanying bilateral hydronephroses and bladder dysfunction with an early diagnosis through prenatal ultrasound and postnatal magnetic resonance imaging. After a timely emergency cesarean section, the infant was administrated antimicrobial prophylaxis and an indwelling catheter treatment. Ultrasound follow-up showed his urinary system gradually developed normally. CONCLUSION: A fetus with bilateral hydronephroses accompanying bladder dysfunction should be observed because of the risk of spontaneous renal rupture with hemorrhage formation. Ultrasound and magnetic resonance imaging play a vital role in the diagnosis and follow-up of Wunderlich syndrome. Early diagnosis facilitates better pregnancy planning and appropriate care of newborns. BioMed Central 2023-05-06 /pmc/articles/PMC10163762/ /pubmed/37147736 http://dx.doi.org/10.1186/s13256-023-03867-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 Jia, Yongmei Gao, Junxia Spontaneous perirenal hemorrhage (Wunderlich syndrome) in the fetus: a case report |
title | Spontaneous perirenal hemorrhage (Wunderlich syndrome) in the fetus: a case report |
title_full | Spontaneous perirenal hemorrhage (Wunderlich syndrome) in the fetus: a case report |
title_fullStr | Spontaneous perirenal hemorrhage (Wunderlich syndrome) in the fetus: a case report |
title_full_unstemmed | Spontaneous perirenal hemorrhage (Wunderlich syndrome) in the fetus: a case report |
title_short | Spontaneous perirenal hemorrhage (Wunderlich syndrome) in the fetus: a case report |
title_sort | spontaneous perirenal hemorrhage (wunderlich syndrome) in the fetus: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10163762/ https://www.ncbi.nlm.nih.gov/pubmed/37147736 http://dx.doi.org/10.1186/s13256-023-03867-4 |
work_keys_str_mv | AT jiayongmei spontaneousperirenalhemorrhagewunderlichsyndromeinthefetusacasereport AT gaojunxia spontaneousperirenalhemorrhagewunderlichsyndromeinthefetusacasereport |