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dc.contributor.authorKarakose, Melia
dc.contributor.authorCaliskan, Mustafa
dc.contributor.authorArslan, Muyesser Sayki
dc.contributor.authorCakal, Erman
dc.contributor.authorYesilyurt, Ahmet
dc.contributor.authorDelibasi, Tuncay
dc.date.accessioned2019-12-10T11:21:02Z
dc.date.available2019-12-10T11:21:02Z
dc.date.issued2015
dc.identifier.issn2359-3997
dc.identifier.urihttps://doi.org/10.1590/2359-3997000000091
dc.identifier.urihttp://hdl.handle.net/11655/15421
dc.description.abstractResistance to thyroid hormone (RTH) is a rare autosomal dominant hereditary disorder. Here in, we report two patients with RTH in whom differentiated thyroid cancer was diagnosed. Two patients were admitted to our clinic and their laboratory results were elevated thyroid hormone levels with unsuppressed TSH. We considered this situation thyroid hormone resistance in the light of laboratory and clinical datas. Thyroid nodule was palpated on physical examination. Thyroid ultrasonography showed multiple nodules in both lobes. Total thyroidectomy was performed. The pathological findings were consistent with papillary thyroid microcarcinoma. BRAFV600E mutation analysis results were negative. RTH is very rare and might be overlooked. There is no consensus on how to overcome the persistently high TSH in patients with RTH and differentiated thyroid cancer (DTC). Further studies are needed to explain the relationship between RTH and DTC which might be helpful for the treatment of these patients.
dc.language.isoen
dc.publisherSbem-Soc Brasil Endocrinologia & Metabologia
dc.relation.isversionof10.1590/2359-3997000000091
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectEndocrinology & Metabolism
dc.titleThyroid Hormone Resistance In Two Patients With Papillary Thyroid Microcarcinoma And Their Brafv600E Mutation Status
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalArchives Of Endocrinology Metabolism
dc.contributor.departmentİç Hastalıkları
dc.identifier.volume59
dc.identifier.issue4
dc.identifier.startpage364
dc.identifier.endpage366
dc.description.indexWoS
dc.description.indexScopus


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