医学
甲状腺
病理
平滑肌肉瘤
甲状腺球蛋白
孤立性纤维性肿瘤
鉴别诊断
组织学
波形蛋白
免疫组织化学
生物
内科学
川地34
干细胞
遗传学
作者
Amal Bennani,Hinde El Fatemi,Ihsane Souaf,Kaouthar Moumna,A. Amarti
标识
DOI:10.1186/1746-1596-8-36
摘要
Primary leiomyosarcomas of the thyroid gland are extremely rare. we report a case of a 72 year-old women with a painful growing mass of the left neck with skin fistula. The patient underwent a lobectomy. The tumor histology showed spindle-shaped cells arranged in interlacing fascicles that expressed desmine and H-caldesmone, but were negative for cytokeratins and thyroglobulin. Total body CT scan didn't show any other tumor. The patient died two months after surgery. Primary thyroid leiomyosarcoma may be mistaken for other tumors, such as anaplastic or medullary carcinomas. Therefore, the diagnosis is difficult and requires numerous clinical, radiological, and pathological investigations.The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1917621950869224.
科研通智能强力驱动
Strongly Powered by AbleSci AI