Periampullary neuroendocrine tumor as a cause of acute pancreatitis

dc.contributor.authorNicolas, Gregory N.
dc.contributor.authorNasser, Haydar A.
dc.contributor.authorHaddad, Juliano
dc.contributor.authorZaghrini, Elie R.
dc.contributor.authorDaher, Karim
dc.contributor.authorNasser, Amal Assef
dc.contributor.authorSaliba, Christian
dc.contributor.authorGharios, Nour
dc.contributor.authorWakim, Raja
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:53:09Z
dc.date.available2025-01-24T11:53:09Z
dc.date.issued2018
dc.description.abstractObjective: Rare disease Background: Duodenal and ampullary carcinoids are very rare tumors accounting respectively for 2% and 0.03% of all carcinoid tumors. Clinical findings vary according to the location of the tumor within the periampullary region; with epigastric pain being the most common presenting symptom in duodenal carcinoids and jaundice the most common clinical finding in ampullary carcinoids. Treatment options include pancreaticoduodenectomy, local excision, and endoscopic excision. Case Report: In this case report, we present a 60-year-old male who presented with a one-week history of intractable epigastric pain. He was diagnosed with duodenal periampullary carcinoid tumor and treated with local excision. Conclusions: Although duodenal and ampullary carcinoid tumors may have different clinical presentations, as well as histo-chemistry characteristics and metastatic potential, they appear to benefit from the same surgical treatment. © Am J Case Rep, 2018.
dc.identifier.doihttps://doi.org/10.12659/AJCR.908205
dc.identifier.eid2-s2.0-85054553545
dc.identifier.pmid30181528
dc.identifier.urihttp://hdl.handle.net/10938/31095
dc.language.isoen
dc.publisherInternational Scientific Information, Inc.
dc.relation.ispartofAmerican Journal of Case Reports
dc.sourceScopus
dc.subjectCarcinoid tumor
dc.subjectGeneral surgery
dc.subjectPancreatic neoplasms
dc.subjectAcute disease
dc.subjectAmpulla of vater
dc.subjectDuodenal neoplasms
dc.subjectHumans
dc.subjectMale
dc.subjectMiddle aged
dc.subjectPancreatitis
dc.subjectChromogranin
dc.subjectCytokeratin antibody
dc.subjectMethylene blue
dc.subjectSynaptophysin
dc.subjectAbdominal tenderness
dc.subjectAcute pancreatitis
dc.subjectAdult
dc.subjectArticle
dc.subjectCase report
dc.subjectCholecystectomy
dc.subjectClinical article
dc.subjectDigestive system examination
dc.subjectEchography
dc.subjectEndoscopic retrograde cholangiopancreatography
dc.subjectEpigastric pain
dc.subjectGallbladder disease
dc.subjectGastrointestinal biopsy
dc.subjectGastrointestinal carcinoid
dc.subjectGastrointestinal endoscopy
dc.subjectHemicolectomy
dc.subjectHuman
dc.subjectHuman tissue
dc.subjectImmunohistochemistry
dc.subjectLocal excision
dc.subjectPatient history of surgery
dc.subjectPhysical examination
dc.subjectScintigraphy
dc.subjectTumor cell
dc.subjectX-ray computed tomography
dc.subjectCarcinoid
dc.subjectComplication
dc.subjectDuodenum tumor
dc.titlePeriampullary neuroendocrine tumor as a cause of acute pancreatitis
dc.typeArticle

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