Publication:
Pancreatic neuroendocrine tumor, lymphoma, and squamous cell carcinoma of hypopharynx; A case report of three primary cancers in one patient

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.date.issuedBE2562
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.format.mimetypeapplication/pdf
dc.identifier.citationInternational Journal of Surgery Case Reports. Vol 65, (2019), p.111-114
dc.identifier.doi10.1016/j.ijscr.2019.10.073
dc.identifier.issn22102612
dc.identifier.other2-s2.0-85074370143
dc.identifier.urihttps://hdl.handle.net/20.500.14740/5697
dc.rights.holderScopus
dc.subject.otherCD20 antigen
dc.subject.otherKi 67 antigen
dc.subject.otherMethotrexate
dc.subject.otherNeuron specific enolase
dc.subject.otherReceptor type tyrosine protein phosphatase C
dc.subject.otherSynaptophysin
dc.subject.otherAdult
dc.subject.otherAntigen expression
dc.subject.otherArticle
dc.subject.otherAxillary lymph node
dc.subject.otherCancer adjuvant therapy
dc.subject.otherCancer diagnosis
dc.subject.otherCancer regression
dc.subject.otherCancer staging
dc.subject.otherCase report
dc.subject.otherChemoradiotherapy
dc.subject.otherClinical article
dc.subject.otherComputer assisted tomography
dc.subject.otherDiabetes mellitus
dc.subject.otherDiffuse large B cell lymphoma
dc.subject.otherDistal pancreatectomy
dc.subject.otherHuman
dc.subject.otherHypertension
dc.subject.otherHypopharynx squamous cell carcinoma
dc.subject.otherImmunohistochemistry
dc.subject.otherIncidental finding
dc.subject.otherInguinal region
dc.subject.otherLymphadenopathy
dc.subject.otherMale
dc.subject.otherMedical history
dc.subject.otherMiddle aged
dc.subject.otherOdynophagia
dc.subject.otherOrchiectomy
dc.subject.otherPancreas islet cell tumor
dc.subject.otherPriority journal
dc.subject.otherRadiation response
dc.subject.otherSmoking
dc.subject.otherSplenectomy
dc.subject.otherSurgical margin
dc.subject.otherTestis tumor
dc.titlePancreatic neuroendocrine tumor, lymphoma, and squamous cell carcinoma of hypopharynx; A case report of three primary cancers in one patient
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85074370143&doi=10.1016%2fj.ijscr.2019.10.073&partnerID=40&md5=5b9a16290d25b029551b8842ea027afa

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