2012
DOI: 10.4103/0971-9261.91088
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Heterotopic pancreas causing duodenal obstruction in a patient previously treated for choledochal cyst

Abstract: A 9-year-old boy presented with duodenal pancreatic rest causing obstruction and required surgical intervention. He had been treated at the age of 4 months for a choledochal cyst. Both choledochal cyst and heterotopic pancreas are entities that are commonly encountered in children, but the incidental presence of both the entities in the same child, albeit presenting metachronously, is extremely rare.

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Cited by 7 publications
(4 citation statements)
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“…The etiology of ectopic pancreas is not clear but several theories have been proposed to explain it. Most accepted theory is that, during embryonic rotation of foregut in a fetus and fusion of dorsal and ventral parts of pancreas, small islands of pancreatic rests are carried away and then they continue to develop at this abnormal new location [11,12]. Heterotopic pancreas is usually an isolated lesion; however multifocal lesions can also be seen.…”
Section: Discussionmentioning
confidence: 99%
“…The etiology of ectopic pancreas is not clear but several theories have been proposed to explain it. Most accepted theory is that, during embryonic rotation of foregut in a fetus and fusion of dorsal and ventral parts of pancreas, small islands of pancreatic rests are carried away and then they continue to develop at this abnormal new location [11,12]. Heterotopic pancreas is usually an isolated lesion; however multifocal lesions can also be seen.…”
Section: Discussionmentioning
confidence: 99%
“…The presence of pancreatic tissue outside its normal localization and without anatomic and vascular continuity with the normal pancreas is termed pancreatic heterotopia (PH) [8]. The incidence reported is 1-2% as per autopsy studies.…”
Section: Discussionmentioning
confidence: 99%
“…However, occasionally they can attain larger sizes and cause symptoms of obstruction [5,6]. PH is a rare condition which is generally asymptomatic, but may present as a cause of GOO [8,9]. We present an unusual case where all the three rare entities caused pyloric obstruction in unison.…”
Section: Introductionmentioning
confidence: 96%
“…Labiausiai priimtina – embriono priekinės žarnos sukimosi bei dorsalinės ir ventralinės kasos dalies susiliejimo metu mažos kasos salelės patenka į įvairias lokalizacijas ir pradeda vystytis į ektopinį kasos audinį atipinėje vietoje (16, 17). Tai galėtų paaiškinti, kodėl dauguma EK būna aplink kasą, daugiausiai virškinamajame trakte, skrandyje, dvylikapirštėje žarnoje, proksimalinėje tuščiosios žarnos dalyje (18).…”
Section: Diskusijaunclassified