Congenital and hereditary cystic diseases of the abdomen

Congenital and hereditary cystic lesions of the abdomen are relatively rare. Correct diagnosis is critical as they may simulate several other benign and malignant acquired diseases of the abdomen. With the correct and appropriate use of imaging, diagnosis may be relatively straightforward and clinic...

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Autores principales: Karaosmanoglu, Ali Devrim, Arslan, Sevtap, Akata, Deniz, Ozmen, Mustafa, Haliloglu, Mithat, Oguz, Berna, Karcaaltincaba, Musturay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Educational Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7406601/
https://www.ncbi.nlm.nih.gov/pubmed/32757136
http://dx.doi.org/10.1186/s13244-020-00898-z
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author Karaosmanoglu, Ali Devrim
Arslan, Sevtap
Akata, Deniz
Ozmen, Mustafa
Haliloglu, Mithat
Oguz, Berna
Karcaaltincaba, Musturay
author_facet Karaosmanoglu, Ali Devrim
Arslan, Sevtap
Akata, Deniz
Ozmen, Mustafa
Haliloglu, Mithat
Oguz, Berna
Karcaaltincaba, Musturay
author_sort Karaosmanoglu, Ali Devrim
collection PubMed
description Congenital and hereditary cystic lesions of the abdomen are relatively rare. Correct diagnosis is critical as they may simulate several other benign and malignant acquired diseases of the abdomen. With the correct and appropriate use of imaging, diagnosis may be relatively straightforward and clinical management may be implemented appropriately. The purpose of this article is to describe imaging findings of common and uncommon congenital and hereditary cystic disease of the abdominal organs.
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spelling pubmed-74066012020-08-13 Congenital and hereditary cystic diseases of the abdomen Karaosmanoglu, Ali Devrim Arslan, Sevtap Akata, Deniz Ozmen, Mustafa Haliloglu, Mithat Oguz, Berna Karcaaltincaba, Musturay Insights Imaging Educational Review Congenital and hereditary cystic lesions of the abdomen are relatively rare. Correct diagnosis is critical as they may simulate several other benign and malignant acquired diseases of the abdomen. With the correct and appropriate use of imaging, diagnosis may be relatively straightforward and clinical management may be implemented appropriately. The purpose of this article is to describe imaging findings of common and uncommon congenital and hereditary cystic disease of the abdominal organs. Springer Berlin Heidelberg 2020-08-05 /pmc/articles/PMC7406601/ /pubmed/32757136 http://dx.doi.org/10.1186/s13244-020-00898-z Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Educational Review
Karaosmanoglu, Ali Devrim
Arslan, Sevtap
Akata, Deniz
Ozmen, Mustafa
Haliloglu, Mithat
Oguz, Berna
Karcaaltincaba, Musturay
Congenital and hereditary cystic diseases of the abdomen
title Congenital and hereditary cystic diseases of the abdomen
title_full Congenital and hereditary cystic diseases of the abdomen
title_fullStr Congenital and hereditary cystic diseases of the abdomen
title_full_unstemmed Congenital and hereditary cystic diseases of the abdomen
title_short Congenital and hereditary cystic diseases of the abdomen
title_sort congenital and hereditary cystic diseases of the abdomen
topic Educational Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7406601/
https://www.ncbi.nlm.nih.gov/pubmed/32757136
http://dx.doi.org/10.1186/s13244-020-00898-z
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