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Wunderlich syndrome with spontaneous renal hemorrhage into renal angiomyolipoma
Wunderlich syndrome is a rarely entity. We report our case of a 60-year-old female, who presented in the emergency medicine department with acute right flank pain, tender mass right upper quadrant abdomen, hypotension, and visible hematuria. Urgent computerized tomogram confirmed bleeding in the rig...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992525/ https://www.ncbi.nlm.nih.gov/pubmed/33776340 http://dx.doi.org/10.4103/UA.UA_169_19 |
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author | Bhatty, Tanweer Zia, Ahmad Khan, Iftikhar Ali Nawaz, Gul |
author_facet | Bhatty, Tanweer Zia, Ahmad Khan, Iftikhar Ali Nawaz, Gul |
author_sort | Bhatty, Tanweer |
collection | PubMed |
description | Wunderlich syndrome is a rarely entity. We report our case of a 60-year-old female, who presented in the emergency medicine department with acute right flank pain, tender mass right upper quadrant abdomen, hypotension, and visible hematuria. Urgent computerized tomogram confirmed bleeding in the right renal angiomyolipoma. Selective angioembolization was done. The patient recovered and was sent home after 1 week. On follow-up after 1 month, she is doing fine, and on ultrasound, AML had interval decrease in size. |
format | Online Article Text |
id | pubmed-7992525 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-79925252021-03-26 Wunderlich syndrome with spontaneous renal hemorrhage into renal angiomyolipoma Bhatty, Tanweer Zia, Ahmad Khan, Iftikhar Ali Nawaz, Gul Urol Ann Case Report Wunderlich syndrome is a rarely entity. We report our case of a 60-year-old female, who presented in the emergency medicine department with acute right flank pain, tender mass right upper quadrant abdomen, hypotension, and visible hematuria. Urgent computerized tomogram confirmed bleeding in the right renal angiomyolipoma. Selective angioembolization was done. The patient recovered and was sent home after 1 week. On follow-up after 1 month, she is doing fine, and on ultrasound, AML had interval decrease in size. Wolters Kluwer - Medknow 2020 2020-10-15 /pmc/articles/PMC7992525/ /pubmed/33776340 http://dx.doi.org/10.4103/UA.UA_169_19 Text en Copyright: © 2020 Urology Annals http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Bhatty, Tanweer Zia, Ahmad Khan, Iftikhar Ali Nawaz, Gul Wunderlich syndrome with spontaneous renal hemorrhage into renal angiomyolipoma |
title | Wunderlich syndrome with spontaneous renal hemorrhage into renal angiomyolipoma |
title_full | Wunderlich syndrome with spontaneous renal hemorrhage into renal angiomyolipoma |
title_fullStr | Wunderlich syndrome with spontaneous renal hemorrhage into renal angiomyolipoma |
title_full_unstemmed | Wunderlich syndrome with spontaneous renal hemorrhage into renal angiomyolipoma |
title_short | Wunderlich syndrome with spontaneous renal hemorrhage into renal angiomyolipoma |
title_sort | wunderlich syndrome with spontaneous renal hemorrhage into renal angiomyolipoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992525/ https://www.ncbi.nlm.nih.gov/pubmed/33776340 http://dx.doi.org/10.4103/UA.UA_169_19 |
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