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A rare diaphragmatic ureteral herniation case report: endoscopic and open reconstructive management
BACKGROUND: Ureteral herniations are a rare occurrence, generally found incidentally on cross sectional imaging or during surgical intervention for unrelated processes. Several locations of ureteral herniations can occur including the inguinal, femoral, sciatic, obturator, and thoracic regions. Whil...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381035/ https://www.ncbi.nlm.nih.gov/pubmed/28381270 http://dx.doi.org/10.1186/s12894-017-0207-5 |
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author | Lin, Frank C. Lin, Jamie S. Kim, Samuel Walker, Jonathan R. |
author_facet | Lin, Frank C. Lin, Jamie S. Kim, Samuel Walker, Jonathan R. |
author_sort | Lin, Frank C. |
collection | PubMed |
description | BACKGROUND: Ureteral herniations are a rare occurrence, generally found incidentally on cross sectional imaging or during surgical intervention for unrelated processes. Several locations of ureteral herniations can occur including the inguinal, femoral, sciatic, obturator, and thoracic regions. While few reports of ureteral hernias are reported in the literature overall, the vast majority of those reported are inguinoscrotal herniations found during evaluation and treatment of inguinal hernias. Pelvic outlet ureteral herniations intrinsically are more common secondary to their dependent locations. Intrathoracic ureteral herniations through diaphragmatic defects are an exceptionally rare subset of ureteral herniations and have only been described sparingly. Fewer than ten case reports of diaphramatic ureteral herniations have been reported and none have described both cystoscopic management and open reconstruction. CASE PRESENTATION: We report the case of a 81 year old female with flank pain who was found to have idiopathic diaphragmatic hernia with incarcerated proximal ureter. She had no prior injury or surgery that explained her clinical presentation. She was initially observed and then managed conservatively with ureteral stent exchanges. Ultimately she underwent open surgical repair of her diaphragmatic hernia, reduction, resection and anastomosis of redundant proximal incarcerated ureteral segment, and nephropexy for a hypermobile right renal unit. This case report illustrates the pre- and post-operative imaging studies of a very rare intrathoracic ureteral herniation as well as surgical approach to repair. CONCLUSION: A herniated ureter is a potential source of serious renal and ureteral complications. The thoracic herniation of ureter is the rarest of the ureteral herniations. When discovered, they should be managed to preserve renal function and prevent strangulation of the affected segment of ureter. This case report documents the treatment of a thoracic ureteral herniation with observation, conservative endoscopic management, and finally open surgical reconstruction. |
format | Online Article Text |
id | pubmed-5381035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53810352017-04-10 A rare diaphragmatic ureteral herniation case report: endoscopic and open reconstructive management Lin, Frank C. Lin, Jamie S. Kim, Samuel Walker, Jonathan R. BMC Urol Case Report BACKGROUND: Ureteral herniations are a rare occurrence, generally found incidentally on cross sectional imaging or during surgical intervention for unrelated processes. Several locations of ureteral herniations can occur including the inguinal, femoral, sciatic, obturator, and thoracic regions. While few reports of ureteral hernias are reported in the literature overall, the vast majority of those reported are inguinoscrotal herniations found during evaluation and treatment of inguinal hernias. Pelvic outlet ureteral herniations intrinsically are more common secondary to their dependent locations. Intrathoracic ureteral herniations through diaphragmatic defects are an exceptionally rare subset of ureteral herniations and have only been described sparingly. Fewer than ten case reports of diaphramatic ureteral herniations have been reported and none have described both cystoscopic management and open reconstruction. CASE PRESENTATION: We report the case of a 81 year old female with flank pain who was found to have idiopathic diaphragmatic hernia with incarcerated proximal ureter. She had no prior injury or surgery that explained her clinical presentation. She was initially observed and then managed conservatively with ureteral stent exchanges. Ultimately she underwent open surgical repair of her diaphragmatic hernia, reduction, resection and anastomosis of redundant proximal incarcerated ureteral segment, and nephropexy for a hypermobile right renal unit. This case report illustrates the pre- and post-operative imaging studies of a very rare intrathoracic ureteral herniation as well as surgical approach to repair. CONCLUSION: A herniated ureter is a potential source of serious renal and ureteral complications. The thoracic herniation of ureter is the rarest of the ureteral herniations. When discovered, they should be managed to preserve renal function and prevent strangulation of the affected segment of ureter. This case report documents the treatment of a thoracic ureteral herniation with observation, conservative endoscopic management, and finally open surgical reconstruction. BioMed Central 2017-04-05 /pmc/articles/PMC5381035/ /pubmed/28381270 http://dx.doi.org/10.1186/s12894-017-0207-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Lin, Frank C. Lin, Jamie S. Kim, Samuel Walker, Jonathan R. A rare diaphragmatic ureteral herniation case report: endoscopic and open reconstructive management |
title | A rare diaphragmatic ureteral herniation case report: endoscopic and open reconstructive management |
title_full | A rare diaphragmatic ureteral herniation case report: endoscopic and open reconstructive management |
title_fullStr | A rare diaphragmatic ureteral herniation case report: endoscopic and open reconstructive management |
title_full_unstemmed | A rare diaphragmatic ureteral herniation case report: endoscopic and open reconstructive management |
title_short | A rare diaphragmatic ureteral herniation case report: endoscopic and open reconstructive management |
title_sort | rare diaphragmatic ureteral herniation case report: endoscopic and open reconstructive management |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381035/ https://www.ncbi.nlm.nih.gov/pubmed/28381270 http://dx.doi.org/10.1186/s12894-017-0207-5 |
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