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A tale of Wünderlich syndrome
Wunderlich syndrome is a rare entity characterized by acute onset of spontaneous, non-traumatic renal hemorrhage into the subcapsular and perirenal spaces. It can be fatal if not promptly recognized clinically and treated aggressively. We report a case of a 63-year-old Caucasian female who was prese...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855280/ https://www.ncbi.nlm.nih.gov/pubmed/24968401 http://dx.doi.org/10.1093/jscr/rjs015 |
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author | Wang, Bonnie H. Pureza, Vincent Wang, Huan |
author_facet | Wang, Bonnie H. Pureza, Vincent Wang, Huan |
author_sort | Wang, Bonnie H. |
collection | PubMed |
description | Wunderlich syndrome is a rare entity characterized by acute onset of spontaneous, non-traumatic renal hemorrhage into the subcapsular and perirenal spaces. It can be fatal if not promptly recognized clinically and treated aggressively. We report a case of a 63-year-old Caucasian female who was presented to the emergency department with acute onset of sharp abdominal and right flank pain, and hypotension. An urgent abdominal and pelvic computed tomography scan with contrast demonstrated a large (13 × 12 × 8.5 cm) right perinephric hematoma of unknown etiology. The patient subsequently underwent renal angiogram that demonstrated active extravasation of the right superior renal artery. She underwent successful embolization procedure and responded well to fluid resuscitation. She remained hemodynamically stable and was discharged home without further events. |
format | Online Article Text |
id | pubmed-3855280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38552802013-12-09 A tale of Wünderlich syndrome Wang, Bonnie H. Pureza, Vincent Wang, Huan J Surg Case Rep Case Reports Wunderlich syndrome is a rare entity characterized by acute onset of spontaneous, non-traumatic renal hemorrhage into the subcapsular and perirenal spaces. It can be fatal if not promptly recognized clinically and treated aggressively. We report a case of a 63-year-old Caucasian female who was presented to the emergency department with acute onset of sharp abdominal and right flank pain, and hypotension. An urgent abdominal and pelvic computed tomography scan with contrast demonstrated a large (13 × 12 × 8.5 cm) right perinephric hematoma of unknown etiology. The patient subsequently underwent renal angiogram that demonstrated active extravasation of the right superior renal artery. She underwent successful embolization procedure and responded well to fluid resuscitation. She remained hemodynamically stable and was discharged home without further events. Oxford University Press 2012-11 2012-12-06 /pmc/articles/PMC3855280/ /pubmed/24968401 http://dx.doi.org/10.1093/jscr/rjs015 Text en Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author 2012. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial reuse, 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 Reports Wang, Bonnie H. Pureza, Vincent Wang, Huan A tale of Wünderlich syndrome |
title | A tale of Wünderlich syndrome |
title_full | A tale of Wünderlich syndrome |
title_fullStr | A tale of Wünderlich syndrome |
title_full_unstemmed | A tale of Wünderlich syndrome |
title_short | A tale of Wünderlich syndrome |
title_sort | tale of wünderlich syndrome |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855280/ https://www.ncbi.nlm.nih.gov/pubmed/24968401 http://dx.doi.org/10.1093/jscr/rjs015 |
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