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dc.contributor.authorNiafar, M
dc.contributor.authorDabiri, S
dc.contributor.authorBozorgi, F
dc.contributor.authorNiafar, F
dc.contributor.authorGholami, N
dc.date.accessioned2018-08-26T08:08:26Z
dc.date.available2018-08-26T08:08:26Z
dc.date.issued2011
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/50329
dc.description.abstractMedullary thyroid carcinoma accounts for 4% of thyroid carcinoma and originates from parafollicular cells, secreting calcitonin and carcinoembryonic antigen (CEA). Conventional radiographic modalities such as Computerized Tomography (CT), Magnetic Resonance Imaging (MRI), and Ultrasonography (U/S), are used for detecting recurrences following total thyroidectomy. However, metastatic disease frequently escapes detection by the above modalities, even when its presence is suggested by persistently elevated serum calcitonin levels. In this paper, we report a case of medullary thyroid carcinoma in a 40 year-old woman who had whole body octreotide scintigraphy to evaluate and detect the origin of calcitonin and CEA secretion.
dc.language.isoEnglish
dc.relation.ispartofJOURNAL OF RESEARCH IN MEDICAL SCIENCES
dc.subjectThyroid cancer
dc.subjectMedullary
dc.subjectCalcitonin
dc.subjectNeoplasm metastasis
dc.titleMetastatic medullary thyroid carcinoma: A case report
dc.typeArticle
dc.citation.volume16
dc.citation.issue4
dc.citation.spage568
dc.citation.epage573
dc.citation.indexWeb of science
dc.citation.URLhttp://jrms.mui.ac.ir/index.php/jrms/article/view/5944


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