Literature DB >> 23575234

[A case of double primary neuroendocrine tumor from duodenum and pancreas].

Dae Won Ma1, Min Kyung Kim, Sun Och Yoon, Kwangwon Rhee, Dong Sup Yoon, Hyojin Park.   

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.

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Year:  2013        PMID: 23575234     DOI: 10.4166/kjg.2013.61.3.155

Source DB:  PubMed          Journal:  Korean J Gastroenterol        ISSN: 1598-9992


  1 in total

1.  Primary retroperitoneal neuroendocrine tumor with nonspecific presentation: A case report.

Authors:  Tareq Hamed Al Taei; Sarah Ali Al Mail; Abdulaziz Hajjaj Al Thinayyan
Journal:  Radiol Case Rep       Date:  2020-07-16
  1 in total

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