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Pancreatic Agenesis with Congenital Diaphragmatic Hernia and Congenital Heart Disease: A Case Report

Pancreatic agenesis is a rare disease that causes neonatal diabetes mellitus and exocrine pancreatic insufficiency. We report the case of a very low birth weight infant with congenital diaphragmatic hernia, and congenital heart disease (ventricular septal defect and patent ductus arteriosus). Failur...

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Autores principales: Nakao, Atsushi, Takeda, Tomohiro, Hisaeda, Yoshiya, Hirota, Atsushi, Amagata, Syusuke, Sakurai, Yuko, Kawakami, Tadashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Medical Publishers 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799714/
https://www.ncbi.nlm.nih.gov/pubmed/24147249
http://dx.doi.org/10.1055/s-0033-1353388
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author Nakao, Atsushi
Takeda, Tomohiro
Hisaeda, Yoshiya
Hirota, Atsushi
Amagata, Syusuke
Sakurai, Yuko
Kawakami, Tadashi
author_facet Nakao, Atsushi
Takeda, Tomohiro
Hisaeda, Yoshiya
Hirota, Atsushi
Amagata, Syusuke
Sakurai, Yuko
Kawakami, Tadashi
author_sort Nakao, Atsushi
collection PubMed
description Pancreatic agenesis is a rare disease that causes neonatal diabetes mellitus and exocrine pancreatic insufficiency. We report the case of a very low birth weight infant with congenital diaphragmatic hernia, and congenital heart disease (ventricular septal defect and patent ductus arteriosus). Failure to gain weight, despite well-managed respiratory and heart failure, was improved by infusion of subcutaneous insulin, administration of pancreatic enzyme, and nutrition of medium-chain-triglyceride -enriched formula. This is the first case of pancreatic agenesis with both malformations where the patient is discharged from the hospital. Early diagnosis and adequate treatments to compensate pancreatic function may prevent mortality and improve growth.
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spelling pubmed-37997142013-10-21 Pancreatic Agenesis with Congenital Diaphragmatic Hernia and Congenital Heart Disease: A Case Report Nakao, Atsushi Takeda, Tomohiro Hisaeda, Yoshiya Hirota, Atsushi Amagata, Syusuke Sakurai, Yuko Kawakami, Tadashi AJP Rep Article Pancreatic agenesis is a rare disease that causes neonatal diabetes mellitus and exocrine pancreatic insufficiency. We report the case of a very low birth weight infant with congenital diaphragmatic hernia, and congenital heart disease (ventricular septal defect and patent ductus arteriosus). Failure to gain weight, despite well-managed respiratory and heart failure, was improved by infusion of subcutaneous insulin, administration of pancreatic enzyme, and nutrition of medium-chain-triglyceride -enriched formula. This is the first case of pancreatic agenesis with both malformations where the patient is discharged from the hospital. Early diagnosis and adequate treatments to compensate pancreatic function may prevent mortality and improve growth. Thieme Medical Publishers 2013-08-14 2013-10 /pmc/articles/PMC3799714/ /pubmed/24147249 http://dx.doi.org/10.1055/s-0033-1353388 Text en © Thieme Medical Publishers
spellingShingle Article
Nakao, Atsushi
Takeda, Tomohiro
Hisaeda, Yoshiya
Hirota, Atsushi
Amagata, Syusuke
Sakurai, Yuko
Kawakami, Tadashi
Pancreatic Agenesis with Congenital Diaphragmatic Hernia and Congenital Heart Disease: A Case Report
title Pancreatic Agenesis with Congenital Diaphragmatic Hernia and Congenital Heart Disease: A Case Report
title_full Pancreatic Agenesis with Congenital Diaphragmatic Hernia and Congenital Heart Disease: A Case Report
title_fullStr Pancreatic Agenesis with Congenital Diaphragmatic Hernia and Congenital Heart Disease: A Case Report
title_full_unstemmed Pancreatic Agenesis with Congenital Diaphragmatic Hernia and Congenital Heart Disease: A Case Report
title_short Pancreatic Agenesis with Congenital Diaphragmatic Hernia and Congenital Heart Disease: A Case Report
title_sort pancreatic agenesis with congenital diaphragmatic hernia and congenital heart disease: a case report
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799714/
https://www.ncbi.nlm.nih.gov/pubmed/24147249
http://dx.doi.org/10.1055/s-0033-1353388
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