Cargando…

An Unusual Case of Choledochal Cyst

Choledochal cyst (CC) is an important surgical cause of jaundice in infants. Infantile variant of CC can mimic biliary atresia in clinical presentation. CC associated with biliary atresia is well described in literature. We encountered an atretic variant of CC that has not been described in literatu...

Descripción completa

Detalles Bibliográficos
Autores principales: Pathak, Manish, Saxena, Rahul, Jayakumar, T.K., Sinha, Arvind, Yadav, Taruna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202579/
https://www.ncbi.nlm.nih.gov/pubmed/30370205
http://dx.doi.org/10.1055/s-0038-1673379
_version_ 1783365706671194112
author Pathak, Manish
Saxena, Rahul
Jayakumar, T.K.
Sinha, Arvind
Yadav, Taruna
author_facet Pathak, Manish
Saxena, Rahul
Jayakumar, T.K.
Sinha, Arvind
Yadav, Taruna
author_sort Pathak, Manish
collection PubMed
description Choledochal cyst (CC) is an important surgical cause of jaundice in infants. Infantile variant of CC can mimic biliary atresia in clinical presentation. CC associated with biliary atresia is well described in literature. We encountered an atretic variant of CC that has not been described in literature ever. The characteristics of this unusual case, management, and proposed hypothesis to its pathogenesis are discussed here.
format Online
Article
Text
id pubmed-6202579
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Georg Thieme Verlag KG
record_format MEDLINE/PubMed
spelling pubmed-62025792018-10-26 An Unusual Case of Choledochal Cyst Pathak, Manish Saxena, Rahul Jayakumar, T.K. Sinha, Arvind Yadav, Taruna European J Pediatr Surg Rep Choledochal cyst (CC) is an important surgical cause of jaundice in infants. Infantile variant of CC can mimic biliary atresia in clinical presentation. CC associated with biliary atresia is well described in literature. We encountered an atretic variant of CC that has not been described in literature ever. The characteristics of this unusual case, management, and proposed hypothesis to its pathogenesis are discussed here. Georg Thieme Verlag KG 2018-01 2018-10-18 /pmc/articles/PMC6202579/ /pubmed/30370205 http://dx.doi.org/10.1055/s-0038-1673379 Text en https://creativecommons.org/licenses/by/4.0/ 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 Pathak, Manish
Saxena, Rahul
Jayakumar, T.K.
Sinha, Arvind
Yadav, Taruna
An Unusual Case of Choledochal Cyst
title An Unusual Case of Choledochal Cyst
title_full An Unusual Case of Choledochal Cyst
title_fullStr An Unusual Case of Choledochal Cyst
title_full_unstemmed An Unusual Case of Choledochal Cyst
title_short An Unusual Case of Choledochal Cyst
title_sort unusual case of choledochal cyst
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202579/
https://www.ncbi.nlm.nih.gov/pubmed/30370205
http://dx.doi.org/10.1055/s-0038-1673379
work_keys_str_mv AT pathakmanish anunusualcaseofcholedochalcyst
AT saxenarahul anunusualcaseofcholedochalcyst
AT jayakumartk anunusualcaseofcholedochalcyst
AT sinhaarvind anunusualcaseofcholedochalcyst
AT yadavtaruna anunusualcaseofcholedochalcyst
AT pathakmanish unusualcaseofcholedochalcyst
AT saxenarahul unusualcaseofcholedochalcyst
AT jayakumartk unusualcaseofcholedochalcyst
AT sinhaarvind unusualcaseofcholedochalcyst
AT yadavtaruna unusualcaseofcholedochalcyst