Morlote Diana, Harada Shuko, Lindeman Brenessa, Stevens Todd M
Department of Pathology, University of Alabama at Birmingham, 3548 North Pavilion, 1802 6th Ave. S, Birmingham, AL, 35249, USA.
Department of Surgery, University of Alabama at Birmingham, Birmingham, AL, USA.
Head Neck Pathol. 2019 Dec;13(4):618-623. doi: 10.1007/s12105-019-01021-5. Epub 2019 Feb 8.
Currently considered a variant of Ewing sarcoma, adamantinoma-like Ewing sarcoma is a rare malignancy that shows classic Ewing sarcoma-associated gene fusions but also epithelial differentiation. Here we present the 6th reported case of adamantinoma-like Ewing sarcoma involving the thyroid gland. Sections of the thyroid tumor from a 20-year old woman showed sheets, lobules and trabeculae of primitive, uniform, small round blue cells that diffusely expressed pankeratin, p40 and CD99. Fluorescent in situ hybridization revealed an EWSR1 gene rearrangement and an EWSR1-FLI1 fusion was detected by RT-PCR. Neck lymph nodes were not involved, and the patient was treated with a Ewing sarcoma chemotherapy protocol and radiation and is disease free 7 months after surgery. The unusual histology and immunohistochemical profile of adamantinoma-like Ewing sarcoma makes diagnosis and classification very challenging. We also present a literature review of adamantinoma-like Ewing sarcoma involving the thyroid.
目前,类造釉细胞瘤样尤因肉瘤被认为是尤因肉瘤的一种变体,是一种罕见的恶性肿瘤,它不仅显示出与经典尤因肉瘤相关的基因融合,还具有上皮分化特征。在此,我们报告第6例累及甲状腺的类造釉细胞瘤样尤因肉瘤病例。一名20岁女性甲状腺肿瘤的切片显示,肿瘤由原始、形态一致的小圆形蓝色细胞构成的片状、小叶状和小梁状结构,这些细胞弥漫性表达全角蛋白、p40和CD99。荧光原位杂交显示EWSR1基因重排,逆转录聚合酶链反应检测到EWSR1-FLI1融合。颈部淋巴结未受累,患者接受了尤因肉瘤化疗方案及放疗,术后7个月无疾病复发。类造釉细胞瘤样尤因肉瘤不同寻常的组织学和免疫组化特征使得诊断和分类极具挑战性。我们还对涉及甲状腺的类造釉细胞瘤样尤因肉瘤进行了文献综述。