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Flood syndrome: a rare case of spontaneous rupture of umbilical hernia in a cirrhotic patient

Flood syndrome is a rare and potentially fatal complication of long-standing ascites resulting from a spontaneous rupture of an umbilical hernia. We present the case of a 67-year-old male with a medical history of diastolic heart failure, cocaine abuse, hepatitis C and cirrhosis secondary to daily a...

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Detalles Bibliográficos
Autores principales: Gorji, Leva, Brown, Jordan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9197296/
https://www.ncbi.nlm.nih.gov/pubmed/35712608
http://dx.doi.org/10.1093/jscr/rjac265
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author Gorji, Leva
Brown, Jordan
author_facet Gorji, Leva
Brown, Jordan
author_sort Gorji, Leva
collection PubMed
description Flood syndrome is a rare and potentially fatal complication of long-standing ascites resulting from a spontaneous rupture of an umbilical hernia. We present the case of a 67-year-old male with a medical history of diastolic heart failure, cocaine abuse, hepatitis C and cirrhosis secondary to daily alcohol consumption who presented to the emergency department with spontaneous rupture of an umbilical hernia with continuous, perfuse drainage of ascites from a 3 cm hernia defect. In this case report, we highlight the successful temporizing and definitive management of flood syndrome, as the patient presented to and was temporized a community hospital and was subsequently transferred to a tertiary care center for definitive management.
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spelling pubmed-91972962022-06-15 Flood syndrome: a rare case of spontaneous rupture of umbilical hernia in a cirrhotic patient Gorji, Leva Brown, Jordan J Surg Case Rep Case Report Flood syndrome is a rare and potentially fatal complication of long-standing ascites resulting from a spontaneous rupture of an umbilical hernia. We present the case of a 67-year-old male with a medical history of diastolic heart failure, cocaine abuse, hepatitis C and cirrhosis secondary to daily alcohol consumption who presented to the emergency department with spontaneous rupture of an umbilical hernia with continuous, perfuse drainage of ascites from a 3 cm hernia defect. In this case report, we highlight the successful temporizing and definitive management of flood syndrome, as the patient presented to and was temporized a community hospital and was subsequently transferred to a tertiary care center for definitive management. Oxford University Press 2022-06-14 /pmc/articles/PMC9197296/ /pubmed/35712608 http://dx.doi.org/10.1093/jscr/rjac265 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author(s) 2022. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Gorji, Leva
Brown, Jordan
Flood syndrome: a rare case of spontaneous rupture of umbilical hernia in a cirrhotic patient
title Flood syndrome: a rare case of spontaneous rupture of umbilical hernia in a cirrhotic patient
title_full Flood syndrome: a rare case of spontaneous rupture of umbilical hernia in a cirrhotic patient
title_fullStr Flood syndrome: a rare case of spontaneous rupture of umbilical hernia in a cirrhotic patient
title_full_unstemmed Flood syndrome: a rare case of spontaneous rupture of umbilical hernia in a cirrhotic patient
title_short Flood syndrome: a rare case of spontaneous rupture of umbilical hernia in a cirrhotic patient
title_sort flood syndrome: a rare case of spontaneous rupture of umbilical hernia in a cirrhotic patient
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9197296/
https://www.ncbi.nlm.nih.gov/pubmed/35712608
http://dx.doi.org/10.1093/jscr/rjac265
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