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Ipsilateral renal dysgenesis or agenesis with tubulocystic anomalies of the mesonephric duct

Tubulocystic anomalies of the mesonephric duct (MND) are a rare group of related entities with a perplexing clinical presentation. Ultrasound is a useful screening investigation, which can help identify a dysplastic kidney or point to renal agenesis and identify cystic or tubulocystic changes in the...

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Autores principales: Joshi, Anagha R., Muthe, Mridula M., Gonapati, Sheethal, Agarwal, Mehak R., Rai, Pareekshith R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AOSIS 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10546241/
https://www.ncbi.nlm.nih.gov/pubmed/37794947
http://dx.doi.org/10.4102/sajr.v27i1.2700
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author Joshi, Anagha R.
Muthe, Mridula M.
Gonapati, Sheethal
Agarwal, Mehak R.
Rai, Pareekshith R.
author_facet Joshi, Anagha R.
Muthe, Mridula M.
Gonapati, Sheethal
Agarwal, Mehak R.
Rai, Pareekshith R.
author_sort Joshi, Anagha R.
collection PubMed
description Tubulocystic anomalies of the mesonephric duct (MND) are a rare group of related entities with a perplexing clinical presentation. Ultrasound is a useful screening investigation, which can help identify a dysplastic kidney or point to renal agenesis and identify cystic or tubulocystic changes in the structures derived from the ureteric bud or MND. Further evaluation with MRI can help in characterisation and direct management. The presence of a dysplastic kidney or absence of a kidney should prompt further evaluation for associated ureteric abnormalities such as ectopic insertion or ureterocoele, which could lead to a diagnosis of tubulocystic anomaly of the MND. CONTRIBUTION: The authors describe two cases, briefly outline the diagnostic approach and summarise the literature on management. Reporting radiologists should be aware of these entities.
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spelling pubmed-105462412023-10-04 Ipsilateral renal dysgenesis or agenesis with tubulocystic anomalies of the mesonephric duct Joshi, Anagha R. Muthe, Mridula M. Gonapati, Sheethal Agarwal, Mehak R. Rai, Pareekshith R. SA J Radiol Case Series Tubulocystic anomalies of the mesonephric duct (MND) are a rare group of related entities with a perplexing clinical presentation. Ultrasound is a useful screening investigation, which can help identify a dysplastic kidney or point to renal agenesis and identify cystic or tubulocystic changes in the structures derived from the ureteric bud or MND. Further evaluation with MRI can help in characterisation and direct management. The presence of a dysplastic kidney or absence of a kidney should prompt further evaluation for associated ureteric abnormalities such as ectopic insertion or ureterocoele, which could lead to a diagnosis of tubulocystic anomaly of the MND. CONTRIBUTION: The authors describe two cases, briefly outline the diagnostic approach and summarise the literature on management. Reporting radiologists should be aware of these entities. AOSIS 2023-09-26 /pmc/articles/PMC10546241/ /pubmed/37794947 http://dx.doi.org/10.4102/sajr.v27i1.2700 Text en © 2023. The Authors https://creativecommons.org/licenses/by/4.0/Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License.
spellingShingle Case Series
Joshi, Anagha R.
Muthe, Mridula M.
Gonapati, Sheethal
Agarwal, Mehak R.
Rai, Pareekshith R.
Ipsilateral renal dysgenesis or agenesis with tubulocystic anomalies of the mesonephric duct
title Ipsilateral renal dysgenesis or agenesis with tubulocystic anomalies of the mesonephric duct
title_full Ipsilateral renal dysgenesis or agenesis with tubulocystic anomalies of the mesonephric duct
title_fullStr Ipsilateral renal dysgenesis or agenesis with tubulocystic anomalies of the mesonephric duct
title_full_unstemmed Ipsilateral renal dysgenesis or agenesis with tubulocystic anomalies of the mesonephric duct
title_short Ipsilateral renal dysgenesis or agenesis with tubulocystic anomalies of the mesonephric duct
title_sort ipsilateral renal dysgenesis or agenesis with tubulocystic anomalies of the mesonephric duct
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10546241/
https://www.ncbi.nlm.nih.gov/pubmed/37794947
http://dx.doi.org/10.4102/sajr.v27i1.2700
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