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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...

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Detalles Bibliográficos
Autores principales: Jhun, Byung Woo, Lee, Kyung-Jong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
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.
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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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