most thyroid neoplasms present as
solitary nodules as incidental findings
ddx is between colloid nodule, adenoma and carcinoma
most thyroid neoplasms
non functional - don’t produce hormones
less than 1% of solitary thyroid nodules are malignant - still many cases because they’re common
most thyroid cancers are indolent - low stage follicular and papillary - 90% 20 year survival
clues to the nature of a thyroid nodule
nodules that take up radioactive iodine
hot nodules
more likely to be benign than malignant
history of radiation exposure is associated with
increased incidence of thyroid malignant
adenomas
benign epithelial tumours
follicular adenoma
hurthle cell adenoma
carcinomas
malignant epithelial tumours
follicular
papillary - common
anaplastic - undifferentiated
medullary - nueroendocrine - carcinoma
adenoma
adenoma nodule
encapsulated and well circumscribed solitary nodule
follicular carcinoma
papillary carcinoma
most common in thyroid cancer
often young women
strong association with ionising radiation
often multifocal - treatment is total thyroidectomy
forms papillae, with crowded cells demonstrating nuclear grooves and clear chromatin, often psammomatous calcification and fibrosis - not encapsulated
lyphatic invasion is common
underlying RET/PTC and BRAF mutations - activate MAPK pathway
good prognosis
prognosis papillary carcinoma
good in young, slightly worse in older
how many foci in papillary carcinoma
ofter multifocal - treatment is total thyroidectomy
papillary carcinoma forms
papillae, with crowded cells demonstrating nuclear grooves and clear chromatin - not encapsulated
anaplastic carcinoma
rare
older patients
often preceded by follicular or papillary thyroid carcinoma
agressive, rapidly enlarging and infiltrative neck mass with mass effect, hoarseness
often metastatic at time of presentation
often multifocal needing thyroidectomy
lymphatic invasion is common to central neck nodes
anaplastic carcinoma metastasis
lose markers of thyroid differentiation by immunochemistry - when four in other organs it is hard to identify the primary tumour
anaplastic carcinoma appearance
anaplastic, pleomorphic cells, mix of large and small, multi nucleation, spindled
medullary carcinoma
neuroendocrine carcinoma of the thyroid
originates from C cells (neuroendocrine cells)
solitary or multifocal, cytologically variable
express neuroendocrine markers and calcitonin by immunochemistry
behaviour variable, metastasise via lymphatics or blood vessels
medullary carcinoma may be preceded by
C cell hyperplasia
medullary carcinoma secrete
most secrete calcitonin and have amyloid in stroma
genetics of medullary carcinoma
associated with MEN2
nearly 100% lifetime risk for those with MEN2
genetics of medullary carcinoma
associated with MEN2
nearly 100% lifetime risk for those with MEN2
medullary carcinoma metastaises via
lymphatics or blood vessels
thyroid function tests
blood tests