Thyroid Nodules Flashcards
How common are thyroid nodules?
nearly 60%
-risk of cancer in a thyroid nodule is small (10-15%), but not insignif
Thyroid neoplasms
Benign: adenoma malignant: papillary (85-90%): multifocal, LN follicular/hurthle (5%): vascular spread Anaplastic (2%) very aggressive medullary (5%) familial
Thyroid adenoma
benign neoplasm -Solitary nodule Follicular / Hurthle cell DDx: hyperplastic nodule follicular carcinoma (to tell difference: evaluate surgical specimen): Careful evaluation of the capsule
Follicular/Hurthle cell carcinoma
two types: minimally invasive (vascular or capsular invasion)
widely invasive: more extensive invasion
Papillary carcinoma
Most common Well-differentiated Multifocal Lymphatic spread Excellent prognosis
-fingerlike papillary projections
-Microscope: nuclear features:
Papillae with vascular core
Optically clear nuclei (“orphan annie eyes”)
Nuclear pseudoinclusions
Nuclear grooves
Rare or absent mitoses
Psammoma Bodies
Anaplastic carcinoma of thyroid gland
Older age group (poor survival) Rapidly growing mass Three patterns: -Spindle cell -Giant cells -Squamoid cells Necrosis and hemorrhage
Medullary carcinoma
Solid proliferation of cells with granular cytoplasm (C cells)
Highly vascular stroma
Hyalinized collagen and/or amyloid
May have Psammoma bodies
Immunostains:
Thyroglobulin -, Calcitonin +, Chromogranin +
Lymphomas
Background autoimmune thyroiditis Large fleshy masses DDx : anaplastic ca of thyroid Positive LCA, usually B-cell Gene rearrangement
Clinical Eval
Hx:
growth
pain
cough, voice change
Physical Exam:
size, consistency, fixation, lymphadenopathy
Irradiation
FH
High clinical suspicion Rapid tumor growth Very firm nodule (rock hard) Fixation to adjacent structures Vocal cord paresis Enlarged regional lymph nodes Family history of PTC or MEN 2 Distant metastases
Approach to pt w/ thyroid nodules
**look at flow chart:
esp get TSH, Diagnostic US, Fine needle aspiration biopsy
Benign: follow most
malignant: surgery
inadequate: rebiopsy
suspicious/indeterminate: scan
Biopsy:
onto slide
alcohol fixative
dipquick stain
Papillary carcinoma of thyroid cytologic features
Highly cellular aspirate \+/- colloid Nuclear enlargement, elongation Nuclear grooves, pseudoinclusions Multiple small to large nucleoli Psammoma bodies (calcifications) Papillary cellular aggregates
Bethesda system
6 diagnostic categories: non-diagnostic benign (0-3%), clinical f/u ACUS (5-15%), repeat FNA suspicious for follicular neoplasm (15-30%) lobectomy susp for malig (60-75%) thyroidectomy malig (97-99%) thyroidectomy
also lists risk of malignancy and usual management
tumors result from
oncogene activation or tumor suppressor gene loss
Papillary cancer mutations
RET (proto-oncogene)/PTC rearrangement mutation (20%)
BRAF point mutation:40% (most common)**
p53 inactivation (point mutation)– normally inhibits cell growth and division
Follicular thyroid cancer
Ras point mutation (PI3K pathway activation in more aggressive tumors)
Pax8-PPARgamma rearrangement (40-50%)
*look at last slide