Publication:
Leiomyosarcoma: A rare tumor of the thyroid

dc.contributor.authorJantima Tanboonen_US
dc.contributor.authorPhawin Keskoolen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-10-19T04:36:19Z
dc.date.available2018-10-19T04:36:19Z
dc.date.issued2013-09-01en_US
dc.description.abstractPrimary leiomyosarcoma of the thyroid gland is uncommon. To date, 20 cases have been reported in English in the literature. The tumors usually present in elderly patients with female predilection and are associated with poor clinical outcome. Herein, we report an additional case of primary thyroid leiomyosarcoma in a 64-year-old woman. She underwent total thyroidectomy and later was discovered to have multiple lung and liver metastases. The patient died 3 months after surgery. The major differential diagnoses including undifferentiated (anaplastic) carcinoma of the thyroid, spindle cell variant of medullary thyroid carcinoma, spindle cell tumor with thymus-like differentiation, uncommon primary tumor of the thyroid and metastatic tumors with predominant spindle cells are discussed. © 2013 Springer Science+Business Media New York.en_US
dc.identifier.citationEndocrine Pathology. Vol.24, No.3 (2013), 136-143en_US
dc.identifier.doi10.1007/s12022-013-9251-1en_US
dc.identifier.issn15590097en_US
dc.identifier.issn10463976en_US
dc.identifier.other2-s2.0-84883489191en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/31226
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84883489191&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleLeiomyosarcoma: A rare tumor of the thyroiden_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84883489191&origin=inwarden_US

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