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A poor prognostic case of mucoepidermoid carcinoma of the thyroid: a case report.

作者信息

Shindo Koji, Aishima Shinichi, Okido Masayuki, Ohshima Akira

机构信息

Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.

出版信息

Case Rep Endocrinol. 2012;2012:862545. doi: 10.1155/2012/862545. Epub 2012 Aug 30.

Abstract

Mucoepidermoid carcinoma (MEC) of the thyroid is very rare and low-grade indolent neoplasm. In past reports of the thyroid MEC, only seven cases were described as poor prognosis. A 91-year-old woman presented with a rapidly growing mass of the left upper neck. She was followed thyroid papillary carcinoma (PC) without operation for two years. Fine needle aspiration cytology (FNAC) showed undifferentiated cells. Total thyroidectomy and bilateral neck dissection were performed. In pathological findings, the tumor had two areas of MEC and PC. The boundary of them was mixed. She died of multiple lung metastases only after four months from the operation. We report a rare case of thyroid MEC which had an aggressive behavior and poor prognosis. This case is a precious in that thyroid MEC occurred during observation of PC and suggests a possibility of the transformation from PC to MEC.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dba/3437277/fe017798e622/CRIM.ENDOCRINOLOGY2012-862545.001.jpg

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