Prolonged Ileus in an Infant Presenting with Primary Congenital Hypothyroidism

Congenital hypothyroidism (CH) is the most common endocrine disorder affecting the newborn. Universal newborn screening (NBS) has virtually eliminated the static encephalopathy and devastating neurodevelopmental syndrome known as cretinism. This report describes the presentation of an infant referre...

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Main Authors: Caroline Chua, Shilpa Gurnurkar, Yahdira Rodriguez-Prado, Victoria Niklas
Format: Article
Language:English
Published: Hindawi Limited 2015-01-01
Series:Case Reports in Pediatrics
Online Access:http://dx.doi.org/10.1155/2015/584735
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spelling doaj-c16303b642d045de9dc98a8c4af1cb192020-11-24T20:45:49ZengHindawi LimitedCase Reports in Pediatrics2090-68032090-68112015-01-01201510.1155/2015/584735584735Prolonged Ileus in an Infant Presenting with Primary Congenital HypothyroidismCaroline Chua0Shilpa Gurnurkar1Yahdira Rodriguez-Prado2Victoria Niklas3Division of Neonatology, Department of Pediatrics, University of Central Florida College of Medicine, Nemours Children’s Hospital, Orlando, FL 32827, USADivision of Endocrinology, Department of Pediatrics, University of Central Florida College of Medicine, Nemours Children’s Hospital, Orlando, FL 32827, USADivision of Neonatology, Department of Pediatrics, University of Central Florida College of Medicine, Nemours Children’s Hospital, Orlando, FL 32827, USADivision of Neonatology and Newborn Services, Olive View UCLA Medical Center, Los Angeles, CA 91342, USACongenital hypothyroidism (CH) is the most common endocrine disorder affecting the newborn. Universal newborn screening (NBS) has virtually eliminated the static encephalopathy and devastating neurodevelopmental syndrome known as cretinism. This report describes the presentation of an infant referred by the primary pediatrician to our hospital at 12 days of age for confirmatory testing after the NBS was consistent with CH. The infant had hypoglycemia secondary to lethargy and poor feeding and required transfer to the neonatal intensive care unit for worsening abdominal distension despite normalization of serum thyroid function tests following hormone replacement. In particular, the recalcitrant ileus and secondary bowel obstruction resulted in an additional diagnostic workup and lengthened hospital day. Our report highlights the acute gastrointestinal consequences of hypothyroidism despite evidence of effective treatment. We believe that the preclinical detection and immediate therapy for CH have lessened the prevalence of this presentation in general practice, and hence practitioners are less likely to be familiar with its natural history and management.http://dx.doi.org/10.1155/2015/584735
collection DOAJ
language English
format Article
sources DOAJ
author Caroline Chua
Shilpa Gurnurkar
Yahdira Rodriguez-Prado
Victoria Niklas
spellingShingle Caroline Chua
Shilpa Gurnurkar
Yahdira Rodriguez-Prado
Victoria Niklas
Prolonged Ileus in an Infant Presenting with Primary Congenital Hypothyroidism
Case Reports in Pediatrics
author_facet Caroline Chua
Shilpa Gurnurkar
Yahdira Rodriguez-Prado
Victoria Niklas
author_sort Caroline Chua
title Prolonged Ileus in an Infant Presenting with Primary Congenital Hypothyroidism
title_short Prolonged Ileus in an Infant Presenting with Primary Congenital Hypothyroidism
title_full Prolonged Ileus in an Infant Presenting with Primary Congenital Hypothyroidism
title_fullStr Prolonged Ileus in an Infant Presenting with Primary Congenital Hypothyroidism
title_full_unstemmed Prolonged Ileus in an Infant Presenting with Primary Congenital Hypothyroidism
title_sort prolonged ileus in an infant presenting with primary congenital hypothyroidism
publisher Hindawi Limited
series Case Reports in Pediatrics
issn 2090-6803
2090-6811
publishDate 2015-01-01
description Congenital hypothyroidism (CH) is the most common endocrine disorder affecting the newborn. Universal newborn screening (NBS) has virtually eliminated the static encephalopathy and devastating neurodevelopmental syndrome known as cretinism. This report describes the presentation of an infant referred by the primary pediatrician to our hospital at 12 days of age for confirmatory testing after the NBS was consistent with CH. The infant had hypoglycemia secondary to lethargy and poor feeding and required transfer to the neonatal intensive care unit for worsening abdominal distension despite normalization of serum thyroid function tests following hormone replacement. In particular, the recalcitrant ileus and secondary bowel obstruction resulted in an additional diagnostic workup and lengthened hospital day. Our report highlights the acute gastrointestinal consequences of hypothyroidism despite evidence of effective treatment. We believe that the preclinical detection and immediate therapy for CH have lessened the prevalence of this presentation in general practice, and hence practitioners are less likely to be familiar with its natural history and management.
url http://dx.doi.org/10.1155/2015/584735
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