Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/12656
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dc.contributor.authorTangsirapat V.
dc.contributor.authorWongta K.
dc.contributor.authorChakrapan Na Ayudhya K.
dc.contributor.authorChakrapan Na Ayudhya V.
dc.contributor.authorSookpotarom P.
dc.date.accessioned2021-04-05T03:04:46Z-
dc.date.available2021-04-05T03:04:46Z-
dc.date.issued2019
dc.identifier.issn22102612
dc.identifier.other2-s2.0-85074370143
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/12656-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85074370143&doi=10.1016%2fj.ijscr.2019.10.073&partnerID=40&md5=5b9a16290d25b029551b8842ea027afa
dc.description.abstractBackground: Pancreatic neuroendocrine tumors (PNETs) are rarely found and the majority of PNETs are nonfunctioning. At present, a patient with pancreatic neuroendocrine tumor (PNET), lymphoma, and squamous cell carcinoma (SCC) occurring simultaneously has not been reported. We presented all these three primary cancers in a same patient. Case presentation: A 51-year-old male presented with a right testicular mass for four months. He underwent right orchidectomy, and the patient was diagnosed malignant diffuse large B-cell lymphoma. Consequently, CHOP regimen and intrathecal methotrexate were given as treatment. During the metastasis work up, a hypodense lesion at the tail of pancreas was found. Distal pancreatectomy and splenectomy were completed, and the pathological report revealed PNET. Eighteen months later, the patient developed a symptom of odynophagia, direct laryngoscopy was performed and a mass at the left arytenoid was found. The biopsy was done and confirmed the diagnosis of SCC. The patient went through concurrent chemo-radiation with a complete response. Currently the patient remains in a complete remission of all three cancers. Discussion: As the patient had non-functioning PNET and was symptom-free, the diagnosis would have not been discovered without the metastasis workup of lymphoma. Although non-functioning PNET less than 2 cm can be safely observed, the tumor was 4.3 × 1.3 cm and adenocarcinoma was suspected, so the patient underwent the surgery. Conclusion: Although many cases with multiple primary cancers have been published, a case of patient with PNET, lymphoma, and SCC occurring as primary cancers has not been yet reported. © 2019 The Author(s)
dc.subjectCD20 antigen
dc.subjectKi 67 antigen
dc.subjectmethotrexate
dc.subjectneuron specific enolase
dc.subjectreceptor type tyrosine protein phosphatase C
dc.subjectsynaptophysin
dc.subjectadult
dc.subjectantigen expression
dc.subjectArticle
dc.subjectaxillary lymph node
dc.subjectcancer adjuvant therapy
dc.subjectcancer diagnosis
dc.subjectcancer regression
dc.subjectcancer staging
dc.subjectcase report
dc.subjectchemoradiotherapy
dc.subjectclinical article
dc.subjectcomputer assisted tomography
dc.subjectdiabetes mellitus
dc.subjectdiffuse large B cell lymphoma
dc.subjectdistal pancreatectomy
dc.subjecthuman
dc.subjecthypertension
dc.subjecthypopharynx squamous cell carcinoma
dc.subjectimmunohistochemistry
dc.subjectincidental finding
dc.subjectinguinal region
dc.subjectlymphadenopathy
dc.subjectmale
dc.subjectmedical history
dc.subjectmiddle aged
dc.subjectodynophagia
dc.subjectorchiectomy
dc.subjectpancreas islet cell tumor
dc.subjectpriority journal
dc.subjectradiation response
dc.subjectsmoking
dc.subjectsplenectomy
dc.subjectsurgical margin
dc.subjecttestis tumor
dc.titlePancreatic neuroendocrine tumor, lymphoma, and squamous cell carcinoma of hypopharynx; A case report of three primary cancers in one patient
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationInternational Journal of Surgery Case Reports. Vol 65, (2019), p.111-114
dc.identifier.doi10.1016/j.ijscr.2019.10.073
Appears in Collections:Scopus 1983-2021

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