外科理论与实践 ›› 2025, Vol. 30 ›› Issue (01): 27-33.doi: 10.16139/j.1007-9610.2025.01.06

• 指南与共识 • 上一篇    下一篇

第5版WHO内分泌和神经内分泌肿瘤分类解读:甲状腺滤泡细胞起源肿瘤的更新及进展

鲁姗姗, 纪元()   

  1. 复旦大学附属中山医院病理科,上海 200032
  • 收稿日期:2024-12-10 出版日期:2025-01-25 发布日期:2025-04-25
  • 通讯作者: 纪元,E-mail:ji.yuan@zs-hospital.sh.cn

Interpretation of the 5th edition of WHO classification of endocrine and neuroendocrine tumors: update and progress on follicular cell-derived thyroid tumors

LU Shanshan, JI Yuan()   

  1. Department of Pathology, Zhongshan Hospital, Fudan University, Shanghai 200032, China
  • Received:2024-12-10 Online:2025-01-25 Published:2025-04-25

摘要:

2022年WHO内分泌和神经内分泌肿瘤分类(第5版)将甲状腺滤泡细胞起源的肿瘤分为良性、低风险和恶性肿瘤。良性肿瘤新增了甲状腺滤泡结节性病变。旧称的“交界性肿瘤”修订为低风险滤泡细胞起源的肿瘤,包括具有乳头样核特征的非浸润性甲状腺滤泡性肿瘤、恶性潜能未定的甲状腺肿瘤以及透明变梁状肿瘤。新版WHO根据分子特征和侵袭性对恶性滤泡细胞起源的肿瘤进行分层。其中具有多种组织亚型的甲状腺乳头状癌(PTC)代表BRAF样恶性肿瘤,而浸润性包裹性滤泡亚型PTC和甲状腺滤泡癌代表RAS样恶性肿瘤。嗜酸细胞癌作为独立类型,特指嗜酸细胞成分≥75%的嗜酸性滤泡细胞起源并缺乏PTC核特征和高级别特征(坏死和核分裂象≥3/2 mm2)的肿瘤。新增的“高级别滤泡细胞起源的甲状腺癌”包括传统甲状腺低分化癌和高级别分化型甲状腺癌。间变性甲状腺癌(ATC)仍是分化最差的类型,甲状腺鳞状细胞癌目前归为ATC的亚型。不再推荐将“甲状腺微小乳头状癌”作为独立亚型;筛状-桑葚型甲状腺癌不再归类为PTC亚型,而被列为组织来源未定的甲状腺肿瘤。

关键词: 甲状腺肿瘤, 甲状腺滤泡细胞, 内分泌和神经内分泌肿瘤, 肿瘤分类, 病理诊断

Abstract:

The 2022 WHO classification of endocrine and neuroendocrine tumors (5th edition) categorizes thyroid follicular cell-derived tumors into benign, low-risk, and malignant types. Benign tumors now include thyroid follicular nodular lesions. A newly added category previously termed "borderline tumors" have been revised to low-risk follicular cell-derived tumors, which encompass non-invasive follicular thyroid neoplasm with papillary-like nuclear features, thyroid tumors of uncertain malignant potential, and hyalinizing trabecular tumors. The new WHO classification stratifies malignant follicular cell-derived tumors based on molecular characteristics and invasiveness: papillary thyroid carcinoma (PTC) with various histological subtypes represents BRAF-like malignancies; invasive encapsulated follicular variant PTC and follicular thyroid carcinoma represent RAS-like malignancies. Oncocytic carcinoma is now recognized as a distinct entity, specifically referring to tumors composed of ≥75% oncocytic follicular cells lacking PTC nuclear features and high-grade characteristics (necrosis and mitotic figures ≥3/2 mm²). A new category termed "high-grade follicular cell-derived thyroid carcinoma" has been added, encompassing traditional poorly differentiated thyroid carcinoma and differentiated high-grade thyroid carcinoma. Anaplastic thyroid carcinoma(ATC) remains the most undifferentiated type, with thyroid squamous cell carcinoma now classified as a subtype of ATC. The term "papillary thyroid microcarcinoma" is no longer recommended as a distinct subtype. Cribriform-morular thyroid carcinoma is no longer classified as a subtype of PTC, but is instead categorized as a tumor of uncertain histogenesis.

Key words: Thyroid tumor, Thyroid follicular cell, Endocrine and neuroendocrine tumor, Tumor classification, Pathological diagnosis

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