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Urachal cyst presenting with huge abscess formation in adults
Urachal disease, a disorder where embryonic remnant of the cloaca and the allantois present after birth as a midline fibrous cord, is usually detected in infancy and childhood. But urachal disease in adults is rare. We report a case of a huge abscess derived from a urachal cyst in an adult. A 52-yea...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Surgical Society
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467394/ https://www.ncbi.nlm.nih.gov/pubmed/23091800 http://dx.doi.org/10.4174/jkss.2012.83.4.254 |
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author | Lee, Sung Hwan Lee, Hyang Im Shin, Dong Gue |
author_facet | Lee, Sung Hwan Lee, Hyang Im Shin, Dong Gue |
author_sort | Lee, Sung Hwan |
collection | PubMed |
description | Urachal disease, a disorder where embryonic remnant of the cloaca and the allantois present after birth as a midline fibrous cord, is usually detected in infancy and childhood. But urachal disease in adults is rare. We report a case of a huge abscess derived from a urachal cyst in an adult. A 52-year-old man presented with peri-umbilical distension and abdominal pain for 2 weeks. Ultrasonography and abdominal computed tomography scan demonstrated a huge abscess derived from the abdominal wall. After prompt incision and drainage, the remaining abscess cavity was removed completely under general anesthesia. Pathologic report was consistent with urachal duct cyst, and the patient was discharged in a week without complication. |
format | Online Article Text |
id | pubmed-3467394 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Korean Surgical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-34673942012-10-22 Urachal cyst presenting with huge abscess formation in adults Lee, Sung Hwan Lee, Hyang Im Shin, Dong Gue J Korean Surg Soc Case Report Urachal disease, a disorder where embryonic remnant of the cloaca and the allantois present after birth as a midline fibrous cord, is usually detected in infancy and childhood. But urachal disease in adults is rare. We report a case of a huge abscess derived from a urachal cyst in an adult. A 52-year-old man presented with peri-umbilical distension and abdominal pain for 2 weeks. Ultrasonography and abdominal computed tomography scan demonstrated a huge abscess derived from the abdominal wall. After prompt incision and drainage, the remaining abscess cavity was removed completely under general anesthesia. Pathologic report was consistent with urachal duct cyst, and the patient was discharged in a week without complication. The Korean Surgical Society 2012-10 2012-09-25 /pmc/articles/PMC3467394/ /pubmed/23091800 http://dx.doi.org/10.4174/jkss.2012.83.4.254 Text en Copyright © 2012, the Korean Surgical Society http://creativecommons.org/licenses/by-nc/3.0 Journal of the Korean Surgical Society is an Open Access Journal. All articles are distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Lee, Sung Hwan Lee, Hyang Im Shin, Dong Gue Urachal cyst presenting with huge abscess formation in adults |
title | Urachal cyst presenting with huge abscess formation in adults |
title_full | Urachal cyst presenting with huge abscess formation in adults |
title_fullStr | Urachal cyst presenting with huge abscess formation in adults |
title_full_unstemmed | Urachal cyst presenting with huge abscess formation in adults |
title_short | Urachal cyst presenting with huge abscess formation in adults |
title_sort | urachal cyst presenting with huge abscess formation in adults |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467394/ https://www.ncbi.nlm.nih.gov/pubmed/23091800 http://dx.doi.org/10.4174/jkss.2012.83.4.254 |
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