Congenital duodenal obstruction with situs inversus totalis: Report of a rare association and discussion

This report is to present and discuss an extremely rare association of situs inversus with duodenal atresia in an 11-day-old male neonate born full term and weighing 1.9 kg. The baby presented with recurrent bilious vomiting. Babygram revealed situs inversus and duodenal obstruction. Echocardiograph...

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Autores principales: Sharma, Satendra, Rashid, Kumar Abdul, Dube, Ravi, Malik, G. K., Tandon, R. K.
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2008
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2788442/
https://www.ncbi.nlm.nih.gov/pubmed/20011474
http://dx.doi.org/10.4103/0971-9261.43029
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author Sharma, Satendra
Rashid, Kumar Abdul
Dube, Ravi
Malik, G. K.
Tandon, R. K.
author_facet Sharma, Satendra
Rashid, Kumar Abdul
Dube, Ravi
Malik, G. K.
Tandon, R. K.
author_sort Sharma, Satendra
collection PubMed
description This report is to present and discuss an extremely rare association of situs inversus with duodenal atresia in an 11-day-old male neonate born full term and weighing 1.9 kg. The baby presented with recurrent bilious vomiting. Babygram revealed situs inversus and duodenal obstruction. Echocardiography showed dextrocardia with a small ASD. Exploration confirmed a duodenal diaphragm with a central perforation between the third and fourth part of the duodenum and situs inversus. The literature search revealed 20 cases reported so far.
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spelling pubmed-27884422009-12-13 Congenital duodenal obstruction with situs inversus totalis: Report of a rare association and discussion Sharma, Satendra Rashid, Kumar Abdul Dube, Ravi Malik, G. K. Tandon, R. K. J Indian Assoc Pediatr Surg Case Report This report is to present and discuss an extremely rare association of situs inversus with duodenal atresia in an 11-day-old male neonate born full term and weighing 1.9 kg. The baby presented with recurrent bilious vomiting. Babygram revealed situs inversus and duodenal obstruction. Echocardiography showed dextrocardia with a small ASD. Exploration confirmed a duodenal diaphragm with a central perforation between the third and fourth part of the duodenum and situs inversus. The literature search revealed 20 cases reported so far. Medknow Publications 2008 /pmc/articles/PMC2788442/ /pubmed/20011474 http://dx.doi.org/10.4103/0971-9261.43029 Text en © Journal of Indian Association of Pediatric Surgeons http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Sharma, Satendra
Rashid, Kumar Abdul
Dube, Ravi
Malik, G. K.
Tandon, R. K.
Congenital duodenal obstruction with situs inversus totalis: Report of a rare association and discussion
title Congenital duodenal obstruction with situs inversus totalis: Report of a rare association and discussion
title_full Congenital duodenal obstruction with situs inversus totalis: Report of a rare association and discussion
title_fullStr Congenital duodenal obstruction with situs inversus totalis: Report of a rare association and discussion
title_full_unstemmed Congenital duodenal obstruction with situs inversus totalis: Report of a rare association and discussion
title_short Congenital duodenal obstruction with situs inversus totalis: Report of a rare association and discussion
title_sort congenital duodenal obstruction with situs inversus totalis: report of a rare association and discussion
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2788442/
https://www.ncbi.nlm.nih.gov/pubmed/20011474
http://dx.doi.org/10.4103/0971-9261.43029
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