Tiemann Thyroid Nodules DSA Flashcards
Incidence of thyroid nodules and cancer
Palpable nodules found in about 5% of adults
Ultrasound studies (or autopsy studies) find nodules in ~50% of adults
Increasing incidence of thyroid nodules found on exams for other reasons
Only about 15% of nodules will be malignant
Incidence of thyroid cancer increasing, but mortality rate remains stable
The task is to identify those nodules that require surgery
work-up of thyroid nodule: history
Identify higher or lower risk groups
Gender–nodules more common in women (x4), but more often malignant in men
Age–malignant nodules more common in ages<30 and >60
History of radiation exposure to head and neck
Family history of thyroid cancer, FAP, MEN, multiple hamartoma syndrome
Voice symptoms, visual symptoms, fatigue, anxiety (Sx of hypo or hyperthyroidism)
workup of thyroid nodule: physical exam, labs, radiology
PHYSICAL EXAM
Character of nodule and thyroid
Solitary vs. multiple
Associated lymphadenopathy (anterior and posterior triangles)
Extrathyroidal manifiestations (voice, eyes, reflexes) looking for signs of hyper or hypo thyroidism
LAB
TSH, T4, T3
RADIOLOGY
Radionuclide scanning if hyperthyroid
Neck ultrasound
FNA
Dependent on technique and pathologist
Best done under US guidance and small-bore needle
Requires pathologist trained in cytopathology
~90% sensitivity and specificity
Indicated for nodules >1cm and/or suspicious on US (hypoechoic, irregular, intranodular vascularity, calcifications, nodal metastases)
May need to aspirate multiple nodules, if more than one meets criteria (up to 4 nodules)
FNA RESULTS
Inadequate specimen
- Requires repeat FNA
Benign
- Requires 6-12 month follow-up (5% false- negative rate)
Malignant
- Requires surgery
Indeterminant (follicular lesion)
- Usually contains follicular cells or Hurthle cells
- Formerly required surgery to examine entire nodule
- — Malignancy in follicular lesions determined by invasion of capsule or follicular cells in surrounding blood vessels or lymphatics
- Now can be further evaluated by gene-expression classifier profile with 90-95% sensitivity and specificity
PAPILLARY CA ON FNA
Little Orphan Annie cells, intra-nuclear grooving, papillary projections, psammoma bodies
SURGICAL TREATMENT OF PAPILLARY CARCINOMA
Total Thyroidectomy +/- Lymph node dissection
Survival rates depend on prognostic factors
Low-Risk vs. High-Risk
Age: <40 vs. >40
Sex: Female vs. male
Extent: Contained vs. capsular invasion, extrathyroidal extension
Metastasis: None vs. regional or distant
Size: <2cm vs. >4cm
Grade: Well-differentiated vs. poorly differentiated
Long-term survival varies from 50%-99%
FNA = FOLLICULAR LESION
Stippled cytoplasm, sheets of cells
FNA = HURTHLE CELLS
Extensive amyloid deposits in the cellular matrix
FNA = INDETERMINATE
Follicular or Hurthle cell lesions
Formerly required the entire nodule for diagnosis to determine invasion of the capsule, lymphatics or blood vessels
Now evaluated first by gene-expression classifier method to determine liklihood of malignancy (NEJM, 2012)
If surgery indicated, lobectomy + isthmusectomy and frozen section
If malignant, then total thyroidectomy, no lymph node dissection
Occasionally FS benign and permanent sections malignant—decision on whether to do completion thyroidectomy dependent on degree of risk
FNA = MEDULLARY CA
Large bi-lobed nuclei with intense staining, Parafollicular C-cells
Medullary carcinoma
Parafollicular “C” cells which secrete calcitonin
5-10% of thyroid cancers, PTC and FTC ~90%
Sporadic (75%) Usually more indolent
Familial (25%)—MEN 2A (60%),2B (5%) or Familial (35%)
Screen for parathyroid and adrenal disease if 2B suspected
Pre-operative calcitonin levels
RET proto-oncogene in patient and relatives
Total thyroidectomy +/- lymph node dissection
Follow-up with serum calcitonin levels or stimulated calcitonin levels
RAI, serum thyroglobulin of no use in follow-up
ANAPLASTIC THYROID CANCER
~ 1% of thyroid cancers
Very aggressive and often presents as a rapidly enlarging, painful mass with obstructive symptoms
Can be diagnosed with FNA
Palliative care only, doesn’t respond well to surgery, radiation therapy, or chemotherapy
FOLLOW-UP OF THYROID CANCERS
Most well-differentiated epithelial thyroid cancer treated with post-op radioactive iodine to ablate subclinical disease or mets
Thyroid replacement
Monitor physical exam and thyroglobulin levels to look for recurrent disease
Medullary cancers followed with calcitonin and family evaluation
Use of PET scan promising, but not yet standard of care
Surgery appropriate for:
Hot” nodule
Toxic nodular goiter
Grave’s Disease, especially in pregnant patient
Multinodular goiter
Surgery usually not performed in thyroiditis with hyperthyroidism
Thyroiditis usually self-limiting