Shah Akeesha A, La Fortune Kristin, Miller Caitlyn, Mills Stacey E, Baloch Zubair, LiVolsi Virginia, Dacic Sanja, Mahaffey Alyssa L, Nikiforova Marina, Nikiforov Yuri E, Seethala Raja R
Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Department of Pathology and Laboratory Medicine, Indiana University Medical Center, Indianapolis, IN, USA.
Mod Pathol. 2017 Mar;30(3):329-339. doi: 10.1038/modpathol.2016.180. Epub 2016 Dec 2.
Sclerosing mucoepidermoid carcinoma with eosinophilia is a rare thyroid neoplasm of uncertain pathogenesis that resembles salivary gland mucoepidermoid carcinoma. This multi-institutional study characterizes the clinicopathologic and molecular features of this tumor by utilizing next-generation sequencing to assess common mutations and gene fusions involved in thyroid carcinogenesis as well as fluorescence in-situ hybridization for MAML2 translocations typical of salivary gland mucoepidermoid carcinoma. Nine cases (6 females and 3 males, mean age: 59 years, range 30-77 years) were identified. All cases were comprised of nests and strands of tumor cells with both squamous and mucinous differentiation embedded in a fibrohyaline stroma with an inflammatory infiltrate replete with eosinophils. All cases were p63 positive, thyroglobulin negative and showed variable expression of TTF-1. All nine cases were negative for MAML2 rearrangements. Five cases successfully tested by next-generation sequencing (ThyroSeq v.2 assay) were negative for mutations and translocations commonly involved in thyroid carcinogenesis. NTRK1 showed overexpression but no evidence of translocation. On follow-up, one patient died of persistent disease, whereas one of four remaining patients with available follow-up (mean: 7.3 years, range 4-11 years) demonstrated recurrence at 4 years. Thus, we show that sclerosing mucoepidermoid carcinoma with eosinophilia appears molecularly and morphologically distinct from follicular and C-cell-derived thyroid tumors as well as from salivary gland mucoepidermoid carcinoma. The overall and recurrence-free survival for these patients may be lower than for other well-differentiated thyroid cancers.
伴嗜酸性粒细胞增多的硬化性黏液表皮样癌是一种发病机制不明的罕见甲状腺肿瘤,类似于涎腺黏液表皮样癌。这项多机构研究通过利用二代测序评估甲状腺癌发生过程中常见的突变和基因融合,以及针对涎腺黏液表皮样癌典型的MAML2易位进行荧光原位杂交,来描述该肿瘤的临床病理和分子特征。共纳入9例患者(6例女性,3例男性,平均年龄59岁,范围30 - 77岁)。所有病例均由巢状和条索状肿瘤细胞组成,肿瘤细胞具有鳞状和黏液样分化,包埋于伴有嗜酸性粒细胞浸润的纤维透明质间质中。所有病例p63均呈阳性,甲状腺球蛋白呈阴性,TTF - 1表达各异。所有9例病例MAML2重排均为阴性。通过二代测序(ThyroSeq v.2检测)成功检测的5例病例,均未发现甲状腺癌发生过程中常见的突变和易位。NTRK1呈过表达,但无易位证据。随访中,1例患者死于疾病持续状态,而其余4例有随访信息的患者中(平均随访7.3年,范围4 - 11年),有1例在4年时复发。因此,我们发现伴嗜酸性粒细胞增多的硬化性黏液表皮样癌在分子和形态上与滤泡性和C细胞来源的甲状腺肿瘤以及涎腺黏液表皮样癌均不同。这些患者的总生存率和无复发生存率可能低于其他高分化甲状腺癌。