dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2016-04-01T18:43:37Z
dc.date.available2016-04-01T18:43:37Z
dc.date.created2016-04-01T18:43:37Z
dc.date.issued2011
dc.identifierClinical Case Studies, v. 2, n. 2, p. 29-31, 2011.
dc.identifier1534-6501
dc.identifierhttp://hdl.handle.net/11449/136976
dc.identifier4880803690413862
dc.identifier4880803690413862
dc.identifier4880803690413862
dc.description.abstractPrimary malignant epithelioid hemangioendothelioma (MEH) of the thyroid is a rare neoplasia with only a few cases reported in the literature. We report a 75 year old man, who presented with a substernal goiter and compressive symptoms. Ultrasonographic evaluation revealed a hypoechogenic nodule in the left lobe, measuring 4.1 cm in maximum diameter, and associated gross calcifications. Fine needle aspiration yielded hemorrhagic material. A left thyroid lobectomy and isthmusectomy was performed. The surgical specimen contained a malignant epithelioid hemangioendothelioma measuring 6 x 4 x 3 cm that had infiltrated about 50% of the thyroidal parenchyma, and surrounded a necrotic nodule. Immunohistochemistry results corroborated the histopathological findings; staining was positive for AE1/AE3, CD31, CD34, factor VIII-related antigen, and Ki-67 expression. Because of the patient’s comorbidities, surgical complementation was not undertaken and he has been undergoing conservative treatment.
dc.languageeng
dc.relationClinical Case Studies
dc.relation0.742
dc.relation0,364
dc.rightsAcesso restrito
dc.sourceCurrículo Lattes
dc.subjectThyroid nodules
dc.subjectHemangioendothelioma
dc.subjectGoiter
dc.subjectRare neoplasia
dc.titleMalignant epitheliod hemangioendothelioma of the thyroid: a case report
dc.typeArtículos de revistas


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