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A right thoracic kidney with a pulmonary vascular malformation in an adult
Ectopic thoracic kidneys are rare anomalies, accounting for less than 5% of all renal ectopia. The anomaly is usually found incidentally on a chest radiograph, with no respiratory or systemic symptoms. It usually presents in the left posteroinferior thorax, associated with a congenital diaphragmatic...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4184529/ https://www.ncbi.nlm.nih.gov/pubmed/25473544 http://dx.doi.org/10.1002/rcr2.8 |
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author | Jhun, Byung Woo Lee, Kyung-Jong |
author_facet | Jhun, Byung Woo Lee, Kyung-Jong |
author_sort | Jhun, Byung Woo |
collection | PubMed |
description | Ectopic thoracic kidneys are rare anomalies, accounting for less than 5% of all renal ectopia. The anomaly is usually found incidentally on a chest radiograph, with no respiratory or systemic symptoms. It usually presents in the left posteroinferior thorax, associated with a congenital diaphragmatic defect or hernia and is more frequent in males than females. Associated anomalies of other organs are rare and inconsistent. We report a case of a 55-year-old female who was referred to our hospital for evaluation of a mass-like lesion in the right chest, identified incidentally on a chest radiograph. Contrast-enhanced chest computed tomography revealed a right ectopic thoracic kidney with a closed diaphragm and an accompanying pulmonary vascular malformation. |
format | Online Article Text |
id | pubmed-4184529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41845292014-12-03 A right thoracic kidney with a pulmonary vascular malformation in an adult Jhun, Byung Woo Lee, Kyung-Jong Respirol Case Rep Case Reports Ectopic thoracic kidneys are rare anomalies, accounting for less than 5% of all renal ectopia. The anomaly is usually found incidentally on a chest radiograph, with no respiratory or systemic symptoms. It usually presents in the left posteroinferior thorax, associated with a congenital diaphragmatic defect or hernia and is more frequent in males than females. Associated anomalies of other organs are rare and inconsistent. We report a case of a 55-year-old female who was referred to our hospital for evaluation of a mass-like lesion in the right chest, identified incidentally on a chest radiograph. Contrast-enhanced chest computed tomography revealed a right ectopic thoracic kidney with a closed diaphragm and an accompanying pulmonary vascular malformation. Blackwell Publishing Ltd 2013-12 2013-10-11 /pmc/articles/PMC4184529/ /pubmed/25473544 http://dx.doi.org/10.1002/rcr2.8 Text en © 2013 The Authors. Respirology Case Reports published by John Wiley & Sons Ltd on behalf of The Asian Pacific Society of Respirology. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Case Reports Jhun, Byung Woo Lee, Kyung-Jong A right thoracic kidney with a pulmonary vascular malformation in an adult |
title | A right thoracic kidney with a pulmonary vascular malformation in an adult |
title_full | A right thoracic kidney with a pulmonary vascular malformation in an adult |
title_fullStr | A right thoracic kidney with a pulmonary vascular malformation in an adult |
title_full_unstemmed | A right thoracic kidney with a pulmonary vascular malformation in an adult |
title_short | A right thoracic kidney with a pulmonary vascular malformation in an adult |
title_sort | right thoracic kidney with a pulmonary vascular malformation in an adult |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4184529/ https://www.ncbi.nlm.nih.gov/pubmed/25473544 http://dx.doi.org/10.1002/rcr2.8 |
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