Thyroid Nodules: Ultrasound Risk, TI-RADS & FNA Pathway
Most thyroid nodules are benign. A disciplined pathway—TSH → ultrasound risk stratification → size-based FNA → cytology-guided management—prevents over-biopsy while catching the cancers that matter.
Step 1 — Initial Clinical & Lab Assessment
- History/Exam: prior neck irradiation, family history (thyroid cancer/MEN2), rapid growth, compressive symptoms (dysphagia, dyspnea, voice change), firm/fixed mass, cervical nodes.
- TSH first.
- Low TSH: order radionuclide thyroid scan. A hyperfunctioning (“hot”) nodule is rarely malignant → usually no FNA; treat hyperthyroidism per guidelines.
- Normal/High TSH: proceed directly to high-quality thyroid ultrasound.
Step 2 — Ultrasound Risk Features (ACR TI-RADS logic)
Assign points for composition, echogenicity, shape, margin, and echogenic foci → sum to a TI-RADS level (TR1–TR5). Key risk cues:
- Higher suspicion: solid hypoechoic, taller-than-wide, irregular/lobulated margins, microcalcifications, extrathyroidal extension, suspicious cervical nodes.
- Lower suspicion: spongiform, partially cystic with comet-tail artifacts, isoechoic/hyperechoic without worrisome features.
Step 3 — Size Thresholds for FNA (typical ACR TI-RADS thresholds)
Use your local protocol; the following are commonly used cutoffs:
- TR1 (benign): no FNA, no routine follow-up.
- TR2 (not suspicious): no FNA; consider follow-up if large or symptomatic.
- TR3 (mildly suspicious): FNA ≥ 2.5 cm; follow-up if ≥1.5 cm.
- TR4 (moderately suspicious): FNA ≥ 1.5 cm; follow-up if ≥1.0 cm.
- TR5 (highly suspicious): FNA ≥ 1.0 cm; follow-up if ≥0.5 cm (or earlier if nodes present).
Symptomatic or compressive nodules can be referred even if below thresholds.
Step 4 — Cervical Nodes Matter
- Any suspicious lymph node (round, cystic, calcifications, peripheral vascularity, loss of hilum) → dedicated US of compartments + FNA of the node (with thyroglobulin washout for PTC suspicion).
Step 5 — Cytology with the Bethesda System
FNA results map to management:
- I — Nondiagnostic: repeat US-guided FNA (optimize technique; consider on-site adequacy).
- II — Benign: US surveillance per risk (often 12–24 months, then lengthen if stable).
- III — AUS/FLUS: repeat FNA and/or consider molecular testing to refine risk; surgical lobectomy if worrisome clinical/US features or positive molecular risk.
- IV — Follicular neoplasm/suspicious for follicular neoplasm: diagnostic lobectomy vs molecular testing to guide extent.
- V — Suspicious for malignancy: surgical referral; extent (lobectomy vs total) individualized.
- VI — Malignant: surgical management with appropriate staging and node evaluation.
Step 6 — Surveillance Intervals (rule-of-thumb)
- High suspicion (TR5) not biopsied or benign cytology: US at ~12 months (earlier if interval growth/symptoms).
- Intermediate (TR4): US 12–24 months.
- Low (TR3): US 1–2 years, then extend if stable.
- Growth definition: ≥20% increase in at least two dimensions (minimum +2 mm) or ≥50% volume increase → consider re-biopsy.
When to Think Beyond the Algorithm
- Childhood neck irradiation, strong family syndromes (MEN2, DICER1, PTEN), rapidly enlarging hard nodule, hoarseness, or fixed mass.
- Substernal goiter with compressive symptoms → CT (without contrast if avoiding iodine pre-RAI) and endocrine/surgical consult.
Special Situations
- Pregnancy: prioritize ultrasound; defer radionuclide scans; surgery only if compelling indications.
- Low TSH “hot” nodules: manage hyperthyroidism (RAI, surgery, or meds). FNA typically not indicated for autonomous nodules lacking suspicious US features.
- Cystic/spongiform nodules: usually benign; aspiration or ethanol ablation for recurrent symptomatic cysts.
Patient FAQs
“Do all nodules need biopsy?” No—ultrasound features and size set rational thresholds so we biopsy only higher-risk nodules.
“If my FNA is benign, why follow it?” A small fraction change over time; periodic ultrasound ensures stability without overtreatment.
References & Notes
Practical pathway aligning with widely used ACR TI-RADS size thresholds and Bethesda cytology actions. Institutions vary—use local protocols and multidisciplinary input. Educational only.