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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Main Authors: Adriana Moreira, MD, André Carvalho, MD, Inês Portugal, MD, José Miguel Jesus, MD
Format: Article
Language:English
Published: Elsevier 2018-02-01
Series:Radiology Case Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1930043317304028
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author Adriana Moreira, MD
André Carvalho, MD
Inês Portugal, MD
José Miguel Jesus, MD
author_facet Adriana Moreira, MD
André Carvalho, MD
Inês Portugal, MD
José Miguel Jesus, MD
author_sort Adriana Moreira, MD
collection DOAJ
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 doaj.art-4f22bcfe4cd1437c993dd5901dadaebe2022-12-21T18:27:59ZengElsevierRadiology Case Reports1930-04332018-02-01131687110.1016/j.radcr.2017.10.025Complete dorsal pancreatic agenesis and unilateral renal agenesisAdriana Moreira, MDAndré Carvalho, MDInês Portugal, MDJosé Miguel Jesus, MDDorsal 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.http://www.sciencedirect.com/science/article/pii/S1930043317304028EmbryogenesisDorsal pancreatic agenesisUrogenital abnormalities
spellingShingle Adriana Moreira, MD
André Carvalho, MD
Inês Portugal, MD
José Miguel Jesus, MD
Complete dorsal pancreatic agenesis and unilateral renal agenesis
Radiology Case Reports
Embryogenesis
Dorsal pancreatic agenesis
Urogenital abnormalities
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 Embryogenesis
Dorsal pancreatic agenesis
Urogenital abnormalities
url http://www.sciencedirect.com/science/article/pii/S1930043317304028
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