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Complete dorsal pancreatic agenesis and unilateral renal agenesis

Dorsal pancreatic agenesis is a very rare congenital anomaly. Unilateral renal agenesis, on the other hand, is a relatively common congenital anomaly, although its etiology is not fully understood. Renal and pancreatic embryologic development appears to be nonrelated. We report a case of a 34-year-o...

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Autores principales: Moreira, Adriana, Carvalho, André, Portugal, Inês, Jesus, José Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5826685/
https://www.ncbi.nlm.nih.gov/pubmed/29487639
http://dx.doi.org/10.1016/j.radcr.2017.10.025
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author Moreira, Adriana
Carvalho, André
Portugal, Inês
Jesus, José Miguel
author_facet Moreira, Adriana
Carvalho, André
Portugal, Inês
Jesus, José Miguel
author_sort Moreira, Adriana
collection PubMed
description Dorsal pancreatic agenesis is a very rare congenital anomaly. Unilateral renal agenesis, on the other hand, is a relatively common congenital anomaly, although its etiology is not fully understood. Renal and pancreatic embryologic development appears to be nonrelated. We report a case of a 34-year-old man who was referred to our hospital for evaluation of cholestasis and microalbuminuria. Ultrasound and magnetic resonance imaging examinations showed empty right renal fossa and absence of the pancreatic neck, body, and tail. Our case report is the second case of a dorsal pancreatic agenesis and unilateral renal agenesis in a young male patient.
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spelling pubmed-58266852018-02-27 Complete dorsal pancreatic agenesis and unilateral renal agenesis Moreira, Adriana Carvalho, André Portugal, Inês Jesus, José Miguel Radiol Case Rep Gastrointestinal Dorsal pancreatic agenesis is a very rare congenital anomaly. Unilateral renal agenesis, on the other hand, is a relatively common congenital anomaly, although its etiology is not fully understood. Renal and pancreatic embryologic development appears to be nonrelated. We report a case of a 34-year-old man who was referred to our hospital for evaluation of cholestasis and microalbuminuria. Ultrasound and magnetic resonance imaging examinations showed empty right renal fossa and absence of the pancreatic neck, body, and tail. Our case report is the second case of a dorsal pancreatic agenesis and unilateral renal agenesis in a young male patient. Elsevier 2017-12-01 /pmc/articles/PMC5826685/ /pubmed/29487639 http://dx.doi.org/10.1016/j.radcr.2017.10.025 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Gastrointestinal
Moreira, Adriana
Carvalho, André
Portugal, Inês
Jesus, José Miguel
Complete dorsal pancreatic agenesis and unilateral renal agenesis
title Complete dorsal pancreatic agenesis and unilateral renal agenesis
title_full Complete dorsal pancreatic agenesis and unilateral renal agenesis
title_fullStr Complete dorsal pancreatic agenesis and unilateral renal agenesis
title_full_unstemmed Complete dorsal pancreatic agenesis and unilateral renal agenesis
title_short Complete dorsal pancreatic agenesis and unilateral renal agenesis
title_sort complete dorsal pancreatic agenesis and unilateral renal agenesis
topic Gastrointestinal
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5826685/
https://www.ncbi.nlm.nih.gov/pubmed/29487639
http://dx.doi.org/10.1016/j.radcr.2017.10.025
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