Review articleThyroid cancer

Overview of the 2022 WHO Classification of Thyroid Neoplasms

Endocr Pathol · 2022Not applicable (review article)
Baloch ZW, Asa SL, Barletta JA, Ghossein RA, Juhlin CC, Jung CK, et al. Endocr Pathol. 2022. 33:27-63
Study type
Review article
Study name
WHO 2022 Thyroid
Design
Narrative review of the changes in the fifth edition of the WHO classification of endocrine and neuroendocrine tumours (thyroid section)
Sample size
Not applicable (review article)
Source
Endocr Pathol · 2022

In plain words

The World Health Organization (WHO) has updated the list and names of the types of thyroid tumour so that pathologists everywhere use a common language. In this classification, tumours are grouped by the cell they start from, how they look under the microscope, their molecular features and how they are likely to behave. This helps make the diagnosis more accurate. For example, some tumours have been placed in a "low-risk" group. If your pathology report uses new names, talk with your treating doctor about what they mean and how they affect your treatment.

Key results

Divided into benign, low-risk and malignant
Follicular cell-derived neoplasms
Low-risk: NIFTP, thyroid tumours of uncertain malignant potential and hyalinising trabecular tumour
Consensus on this term
Thyroid follicular nodular disease (FND)
For multifocal hyperplastic/neoplastic lesions in the setting of multinodular goitre
Papillary carcinoma (PTC): BRAF-like; invasive encapsulated follicular variant of PTC and follicular carcinoma: RAS-like
Molecular classification of follicular malignancies
Requires careful subtyping; recommended not to be recorded as a PTC subtype
Papillary microcarcinoma
No longer a subtype of PTC
Cribriform-morular carcinoma
Listed among tumours of uncertain histogenesis
Its use is not recommended
The term "Hürthle cell"
Because it is a misnomer
A distinct entity: more than 75% oncocytic cells, without PTC nuclear features and without high-grade features
Oncocytic carcinoma
High-grade features: necrosis and at least 5 mitoses per 2 mm²
Include conventional poorly differentiated carcinoma and high-grade differentiated thyroid carcinomas
High-grade follicular cell-derived malignancies
Both with increased mitotic activity and tumour necrosis, without anaplastic histology, and with similar clinical behaviour
Now a subtype of anaplastic carcinoma
Squamous cell carcinoma of the thyroid
Introduction of a grading system based on mitotic count, tumour necrosis and Ki67 index
Medullary thyroid carcinoma
A separate section for mixed C-cell and follicular cell tumours
Salivary gland-type carcinomas of the thyroid; thymic tumours within the thyroid; thyroblastoma
New categories
Thyroblastoma is a rare embryonal tumour associated with DICER1 mutations

Study population

Not applicable. This article did not enrol patients; it reviews the changes in the histological and molecular classification of thyroid neoplasms.

Endpoints

Not applicable. This is a review article and no clinical endpoint is defined. It focuses on changes in the classification, nomenclature and diagnostic criteria of thyroid tumours.

Safety and side effects

Not applicable. This is a review article on classification and reports no treatment adverse events.

Clinical significance and place in guidelines

This article summarises the fifth edition of the WHO classification of thyroid tumours, which changes pathology nomenclature and reporting criteria: division of follicular cell-derived tumours into benign, low-risk and malignant; separation of BRAF-like and RAS-like malignancies; definition of high-grade malignancies; grading of medullary carcinoma; and new categories such as thyroblastoma. The abstract makes no statement on changes to treatment protocols or endorsement in clinical guidelines; the adoption of these changes in treatment guidelines should be checked separately.

Limitations

This article is a narrative review of a consensus classification and gives no data on patients' clinical outcomes. The abstract does not state the level of evidence for the changes. The practical effect of this classification on treatment decisions should be checked in the full text and clinical guidelines.

This summary was prepared by the editorial team from the published paper; the original paper is the final reference. Read the original abstract on PubMed.