A case of double primary neuroendocrine tumor from duodenum and pancreas

Dae W.on Ma, Min K.yung Kim, SunOch Yoon, Kwangwon Rhee, Dong S.up Yoon, HyoJin Park

Research output: Contribution to journalArticle

Abstract

Gastrointestinal neuroendocrine tumors arise from cells of the diffuse neuroendocrine system and can take place almost anywhere within the gastrointestinal tract. A 40-year-old man admitted to evaluate a duodenal subepithelial lesion which was incidentally found at health check-up. The polypoid duodenal subepithelial lesion, measuring about 7 mm, was removed by the endoscopic mucosal resection and the pathology confirmed a neuroendocrine tumor. Abdominopelvic computed tomography, done for staging work up, revealed a mass in the pancreatic head and the patient received pylorus preserving pancreaticoduodenectomy. Mass at the pancreas also found out to be neuroendocrine tumor but showed different histopathologic traits under immunohistochemical staining. The patient was also diagnosed as hyperparathyroidism and pituitary microadenoma. Finally, multiple endocrine neoplasia type 1 was confirmed, which was accompanied by duodenal neuroendocrine tumor.

Original languageEnglish
Pages (from-to)155-159
Number of pages5
JournalThe Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi
Volume61
Issue number3
Publication statusPublished - 2013 Mar 25

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Neuroendocrine Tumors
Duodenum
Pancreas
Multiple Endocrine Neoplasia Type 1
Neurosecretory Systems
Pancreaticoduodenectomy
Hyperparathyroidism
Pylorus
Gastrointestinal Tract
Tomography
Pathology
Staining and Labeling
Health

All Science Journal Classification (ASJC) codes

  • Medicine(all)

Cite this

Ma, Dae W.on ; Kim, Min K.yung ; Yoon, SunOch ; Rhee, Kwangwon ; Yoon, Dong S.up ; Park, HyoJin. / A case of double primary neuroendocrine tumor from duodenum and pancreas. In: The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi. 2013 ; Vol. 61, No. 3. pp. 155-159.
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A case of double primary neuroendocrine tumor from duodenum and pancreas. / Ma, Dae W.on; Kim, Min K.yung; Yoon, SunOch; Rhee, Kwangwon; Yoon, Dong S.up; Park, HyoJin.

In: The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi, Vol. 61, No. 3, 25.03.2013, p. 155-159.

Research output: Contribution to journalArticle

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AU - Ma, Dae W.on

AU - Kim, Min K.yung

AU - Yoon, SunOch

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AU - Yoon, Dong S.up

AU - Park, HyoJin

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AB - Gastrointestinal neuroendocrine tumors arise from cells of the diffuse neuroendocrine system and can take place almost anywhere within the gastrointestinal tract. A 40-year-old man admitted to evaluate a duodenal subepithelial lesion which was incidentally found at health check-up. The polypoid duodenal subepithelial lesion, measuring about 7 mm, was removed by the endoscopic mucosal resection and the pathology confirmed a neuroendocrine tumor. Abdominopelvic computed tomography, done for staging work up, revealed a mass in the pancreatic head and the patient received pylorus preserving pancreaticoduodenectomy. Mass at the pancreas also found out to be neuroendocrine tumor but showed different histopathologic traits under immunohistochemical staining. The patient was also diagnosed as hyperparathyroidism and pituitary microadenoma. Finally, multiple endocrine neoplasia type 1 was confirmed, which was accompanied by duodenal neuroendocrine tumor.

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