The conventional classification based on morphology and clinical features is largely supported by molecular data currently available. Genetic profiles of four main categories appear distinctly different from each other with a few areas of overlap.
The classification of thyroid tumors modified from WHO classification (2004) is as follows:
Tumors of Follicular Epithelium:
■Follicular adenoma (including Hurthle cell adenoma)
■Hyalinizing trabecular adenoma ■Follicular carcinoma (including Hurthle cell carcinoma)
– Minimally invasive – – Widely invasive
■Papillary carcinomas
■Poorly differentiated carcinoma ■Anaplastic carcinoma
■Squamous cell carcinoma ■Mucoepidermoid carcinoma ■Sclerosing mucoepidermoid carcinoma with eosinophilia ■Mucinous carcinoma
Tumors with C Cell Differentiation
Medullary carcinoma
Tumors with Mixed Differentiation
■Collision tumor—follicular/papillary or follicular/medullary
■Mixed differentiated carcinoma intermediate type
Tumors Showing Thymic or Related Branchial Pouch Differentiation
■Ectopic thymoma
■Spindle epithelial tumor with thymus-like
element (SETTLE)
■Carcinoma showing thymus-like element (CASTLE).
Tumors of Lymphoid Cells
■Malignant lymphoma ■Plasmacytoma
Mesenchymal Tumors
■Smooth muscle tumors ■Peripheral nerve sheath tumors ■Paragangliomas
■Solitary fibrous tumors ■Follicular dendritic cell tumors ■LCH
■Angiosarcoma.
Teratomas
Secondaries
