A PATIENT WITH AN ATYPIC NECK MASS LESION

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dc.authoridGÖKÇAY CANPOLAT, ASENA/0000-0003-1186-2960
dc.authoridCANPOLAT, ASENA/0000-0003-1186-2960
dc.authoridKorkmaz, Fatma Nur Nur/0000-0002-3994-8320
dc.authorwosidGÖKÇAY CANPOLAT, ASENA/AAB-9310-2022
dc.authorwosidCANPOLAT, ASENA/AAH-1447-2020
dc.authorwosidKorkmaz, Fatma Nur Nur/IZP-6196-2023
dc.contributor.authorKorkmaz, F. N.
dc.contributor.authorCanpolat, A. Gokcay
dc.contributor.authorBilezikci, B.
dc.contributor.authorGurkan, H.
dc.contributor.authorErdogan, M. F.
dc.date.accessioned2024-06-12T11:12:03Z
dc.date.available2024-06-12T11:12:03Z
dc.date.issued2020
dc.departmentTrakya Üniversitesien_US
dc.description.abstractAn 81-year-old woman presented with a history of essential hypertension for eight years and an asymptomatic multinodular goiter that had been incidentally discovered on neck ultrasonography two years ago and an-isohypoechoic mass lesion located adjacent to the right lobe inferior pole of the thyroid gland. Parathyroid adenoma or lymphadenopathy were the differential diagnosis. After two years, the endocrine surgeon decided to operate her multinodular goiter and her probably benign lesion. intraoperatively, the blood pressure and pulse rate increased markedly and intravenous antihypertensive treatment was administered. She was discharged after blood pressure control. A 2 mm micromedullary thyroid carcinoma with C-cell hyperplasia located on the left lobe of the thyroid was detected. The aforementioned mass lesion was also reported as typical cervical paraganglioma. Because of concomitant medullary thyroid carcinoma with C-cell hyperplasia and paraganglioma the patient was subjected to genetic counseling and molecular testing for hereditary cancer syndromes. A variation of the succinate dehydrogenase gene D (SDHD) NM_003002.3: c.325C> T (Gln109Term) has been reported as the disease-causing mutation. Herein we present a case diagnosed for neck paraganglioma and medullary thyroid carcinoma after an intraoperative hypertensive crisis.en_US
dc.identifier.doi10.4183/aeb.2020.232
dc.identifier.endpage235en_US
dc.identifier.issn1841-0987
dc.identifier.issn1843-066X
dc.identifier.issue2en_US
dc.identifier.pmid33029241en_US
dc.identifier.scopus2-s2.0-85092506777en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage232en_US
dc.identifier.urihttps://doi.org/10.4183/aeb.2020.232
dc.identifier.urihttps://hdl.handle.net/20.500.14551/23023
dc.identifier.volume16en_US
dc.identifier.wosWOS:000597111200016en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherEditura Acad Romaneen_US
dc.relation.ispartofActa Endocrinologica-Bucharesten_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectParagangliomaen_US
dc.subjectThyroid Noduleen_US
dc.subjectHypertensive Crisisen_US
dc.subjectSDHD Geneen_US
dc.subjectPheochromocytomaen_US
dc.subjectParagangliomaen_US
dc.subjectResectionen_US
dc.subjectHeaden_US
dc.titleA PATIENT WITH AN ATYPIC NECK MASS LESIONen_US
dc.typeArticleen_US

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