Combined pancreatic and gastric heterotopia in small intestine presenting as intussusception—A rare congenital anomaly
Pancreatic and gastric heterotopias are rare congenital anomalies which have been reported throughout the length of the gastrointestinal tract. Combined gastric and pancreatic heterotopias, although very rare, have been described mainly in the duodenum followed by jejunum with ileum being a rare sit...
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Wolters Kluwer Medknow Publications
2021
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oai:doaj.org-article:fd5bfd44a2824ca6b343fdef2da56a802021-12-02T19:27:27ZCombined pancreatic and gastric heterotopia in small intestine presenting as intussusception—A rare congenital anomaly0377-492910.4103/IJPM.IJPM_662_20https://doaj.org/article/fd5bfd44a2824ca6b343fdef2da56a802021-01-01T00:00:00Zhttp://www.ijpmonline.org/article.asp?issn=0377-4929;year=2021;volume=64;issue=5;spage=175;epage=177;aulast=Singhhttps://doaj.org/toc/0377-4929Pancreatic and gastric heterotopias are rare congenital anomalies which have been reported throughout the length of the gastrointestinal tract. Combined gastric and pancreatic heterotopias, although very rare, have been described mainly in the duodenum followed by jejunum with ileum being a rare site. The reported incidence of this combined heterotopias is low, ranging from <1% to 13%. Extensive literature search has revealed that only Four cases of combined pancreatic and gastric heterotopias have been reported in the small intestine till date. Hence, we report this case for its rarity and unusual presentation as intussusception in a young male.Tejasvita SinghSonal TripathiShatakshee TewariKachnar VarmaVatsala MisraWolters Kluwer Medknow Publicationsarticleileumintussceptionmixed gastric and pancreatic heterotopiasPathologyRB1-214MicrobiologyQR1-502ENIndian Journal of Pathology and Microbiology, Vol 64, Iss 5, Pp 175-177 (2021) |
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ileum intussception mixed gastric and pancreatic heterotopias Pathology RB1-214 Microbiology QR1-502 |
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ileum intussception mixed gastric and pancreatic heterotopias Pathology RB1-214 Microbiology QR1-502 Tejasvita Singh Sonal Tripathi Shatakshee Tewari Kachnar Varma Vatsala Misra Combined pancreatic and gastric heterotopia in small intestine presenting as intussusception—A rare congenital anomaly |
description |
Pancreatic and gastric heterotopias are rare congenital anomalies which have been reported throughout the length of the gastrointestinal tract. Combined gastric and pancreatic heterotopias, although very rare, have been described mainly in the duodenum followed by jejunum with ileum being a rare site. The reported incidence of this combined heterotopias is low, ranging from <1% to 13%. Extensive literature search has revealed that only Four cases of combined pancreatic and gastric heterotopias have been reported in the small intestine till date. Hence, we report this case for its rarity and unusual presentation as intussusception in a young male. |
format |
article |
author |
Tejasvita Singh Sonal Tripathi Shatakshee Tewari Kachnar Varma Vatsala Misra |
author_facet |
Tejasvita Singh Sonal Tripathi Shatakshee Tewari Kachnar Varma Vatsala Misra |
author_sort |
Tejasvita Singh |
title |
Combined pancreatic and gastric heterotopia in small intestine presenting as intussusception—A rare congenital anomaly |
title_short |
Combined pancreatic and gastric heterotopia in small intestine presenting as intussusception—A rare congenital anomaly |
title_full |
Combined pancreatic and gastric heterotopia in small intestine presenting as intussusception—A rare congenital anomaly |
title_fullStr |
Combined pancreatic and gastric heterotopia in small intestine presenting as intussusception—A rare congenital anomaly |
title_full_unstemmed |
Combined pancreatic and gastric heterotopia in small intestine presenting as intussusception—A rare congenital anomaly |
title_sort |
combined pancreatic and gastric heterotopia in small intestine presenting as intussusception—a rare congenital anomaly |
publisher |
Wolters Kluwer Medknow Publications |
publishDate |
2021 |
url |
https://doaj.org/article/fd5bfd44a2824ca6b343fdef2da56a80 |
work_keys_str_mv |
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