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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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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. |
format | Online Article Text |
id | pubmed-5826685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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