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伴有嗜酸粒细胞增多的甲状腺硬化性黏蛋白样癌合并腮腺基底细胞腺瘤:细胞学、组织学和分子特征。

Thyroid sclerosing mucoepidermoid carcinoma with eosinophilia in conjunction with parotid basal cell adenoma: Cytologic, histologic, and molecular features.

机构信息

Department of Pathology, University of Rochester, Rochester, New York, USA.

Department of Pathology, Ohio State University Wexner Medical Center, Columbus, Ohio, USA.

出版信息

Diagn Cytopathol. 2021 Jul;49(7):E262-E268. doi: 10.1002/dc.24701. Epub 2021 Jan 23.

Abstract

Sclerosing mucoepidermoid carcinoma with eosinophilia (SMECE) is a rare malignancy in the thyroid: only 56 cases with histologic descriptions are reported in the literature and fewer reports describe the cytomorphology. Given the rarity of SMECE, data on the cytomorphologic and molecular features are limited. We report a case of a 53-year-old woman with a 5 cm left thyroid mass. Fine-needle aspiration (FNA) revealed atypia of undetermined significance and pathology of left thyroid lobectomy specimen showed SMECE. Additionally, a left pre-auricular lump was noted and FNA followed by left superficial parotidectomy showed basal cell adenoma. Next-generation sequencing showed point mutations in NTRK3 and NF1. Unlike salivary gland mucoepidermoid carcinoma, MAML2 translocations are not present in SMECE. Even though it is a rare entity, awareness of SMECE of the thyroid is important. In this case report we review the cytomorphologic, histologic, and molecular features.

摘要

伴有嗜酸性粒细胞增多的硬化型黏液表皮样癌(SMECE)是甲状腺的一种罕见恶性肿瘤:文献中仅报道了 56 例具有组织学描述的病例,并且较少有报道描述其细胞形态学特征。鉴于 SMECE 的罕见性,关于其细胞形态学和分子特征的数据有限。我们报告了一例 53 岁女性,其左侧甲状腺有 5cm 大的肿块。细针抽吸(FNA)显示意义未明的非典型性,左甲状腺叶切除术标本的病理显示为 SMECE。此外,还发现左侧耳前有一个肿块,行 FNA 后行左侧腮腺浅叶切除术显示基底细胞腺瘤。下一代测序显示 NTRK3 和 NF1 的点突变。与唾液腺黏液表皮样癌不同,SMECE 中不存在 MAML2 易位。尽管它是一种罕见实体,但认识甲状腺的 SMECE 很重要。在本病例报告中,我们回顾了其细胞形态学、组织学和分子特征。

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