Thyroid Papillary Carcinoma
Benign nodular Goiter
Toxic nodules
Benign Neoplasms
Malignant Neoplasms
About 1% of all cancers
80% of all thyroid cancers
Can present in any age group
Mainly in adults, ages 20-40
Females more affected than males
Indolent and non-aggressive
Commonly, tumor may invade lymphatics leading to multifocal lesions, presenting with enlarged lymph nodes within the neck region (lymphadenopathy)
Vascular invasion rare
Radiation
Autoimmune diseases, such as Graves disease
Certain genetic syndromes, such as familial adenomatous polyposis coli
Encapsulated Variant – well encapsulated
Papillary Microcarcinoma
Follicular Variant – follicular architecture
Tall Cell Variant -
Columnar Cell Variant
Can arise anywhere in gland
Average 2 cm
Appear as firm, white, lesions, often with scars and cysts
Presence of necrosis signifies an aggressive lesion
Can often see papillary foci
Usually papilla
Psammoma bodies, which are collections of dead papillae cells, with calcium deposition
Nuclei are round, clear and empty looking
Areas of squamous differentiation
Monoclonal proliferation
RET oncogene rearrangements
Poor Prognosis
Male, young, large mass and presence of cells outside of thyroid
Not used as far majority are low-grade, grade 1
Thyrogloblin
Cytokeratin-19
HBME-1
Cytokeratin
Epithelial cells
Thyroglobulin
Thyroid cancer
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