Primary Extra-Osseous Ewing Sarcoma of the Thyroid: A Case Report and Review of the Literature.

IF 4.1
Head and neck pathology Pub Date : 2022-06-01 Epub Date: 2021-07-26 DOI:10.1007/s12105-021-01365-x
Amanda H Seipel, Hiba Mechahougui, Nicolas Mach, Frédéric Triponez, William C Faquin, Claudio De Vito
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引用次数: 4

Abstract

Extra-osseous Ewing sarcoma (ES) is a rare and aggressive malignant tumor found in a variety of organs. Primary ES of the thyroid is exceedingly rare and few cases have been documented to date. We describe the case of a 54-year old woman with a history of breast carcinoma in whom a unique hypermetabolic left thyroid nodule was identified during a follow-up PET-CT scan. An ultrasound examination showed a hypoechogenic nodule of 3.7 cm. A cytological diagnosis of poorly differentiated thyroid carcinoma was made, and a total thyroidectomy was performed. The surgical specimen revealed a poorly differentiated neoplasm composed of medium-sized cells with scant cytoplasm, expressing pancytokeratin, CD99 and NKX2.2 but lacking p63 and p40 expression. Molecular analysis revealed a EWSR1-FLI1 fusion transcript supporting the diagnosis of a primary extra-osseous ES of the thyroid. The patient received adjuvant chemotherapy and has no evidence of recurrent disease.

Abstract Image

Abstract Image

原发性甲状腺骨外尤文氏肉瘤1例报告及文献复习。
骨外尤文氏肉瘤(ES)是一种罕见的侵袭性恶性肿瘤,可在多种器官中发现。原发性甲状腺ES极为罕见,至今仅有少数病例被记录在案。我们描述了一个54岁的女性乳腺癌病史,在随访PET-CT扫描中发现了一个独特的高代谢左甲状腺结节。超声检查显示低回声结节3.7厘米。经细胞学诊断为低分化甲状腺癌,并行甲状腺全切除术。手术标本显示为低分化肿瘤,由中等大小的细胞组成,细胞质较少,表达泛细胞角蛋白、CD99和NKX2.2,但缺乏p63和p40的表达。分子分析显示EWSR1-FLI1融合转录物支持原发性甲状腺骨外ES的诊断。患者接受了辅助化疗,无复发迹象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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