Management of TI-RADS 3 Thyroid Nodules with Bilateral Involvement
For this patient with TI-RADS 3 bilateral thyroid nodules, the largest measuring 1.06 cm, obtain thyroid function tests (TSH) immediately and schedule ultrasound follow-up in 12 months, as none of the nodules meet the 1.5 cm threshold for fine-needle aspiration biopsy. 1, 2
Immediate Next Steps
Laboratory Assessment
- Measure serum TSH as the first-line thyroid function test to assess functional status of the nodules and exclude hyperthyroidism or hypothyroidism 1, 2, 3
- Complete thyroid function panel if TSH is abnormal 1
Size-Based Management Decision
The American College of Radiology TI-RADS system provides clear size thresholds for FNA biopsy based on risk category 1, 2:
- TI-RADS 3 nodules require FNA only if ≥1.5 cm 1, 2, 3
- Your largest nodule measures 1.06 cm in the right lobe, which is below the FNA threshold 1
- The left lobe nodules (0.56 cm and 0.44 cm) are also well below this threshold 1
Surveillance Strategy
Follow-Up Imaging Timeline
- Schedule ultrasound follow-up in 12 months for nodules not meeting FNA criteria 1, 2
- Alternative acceptable range is 6-12 months per ACR guidelines 2, 3
- The 12-month interval is appropriate given the low-risk features: smooth borders, isoechoic appearance, no calcifications, and no intranodular vascularity 1, 4
What to Monitor on Follow-Up
Assess for these concerning changes that would prompt FNA 1, 2:
- Growth to ≥1.5 cm in any dimension (primary trigger for biopsy)
- Development of suspicious features: irregular margins, microcalcifications, marked hypoechogenicity, or taller-than-wide shape
- New intranodular vascularity on color Doppler
- Emergence of suspicious cervical lymph nodes
Risk Assessment Based on Current Features
Favorable Characteristics Present
Your nodules demonstrate multiple reassuring features that support the TI-RADS 3 classification 1, 4:
- Smooth, well-defined borders (associated with benign nodules) 2, 4
- Isoechoic appearance (intermediate risk, not the high-risk hypoechoic or very hypoechoic pattern) 2, 4
- No calcifications (absence of punctate echogenic foci, which carry 72% association with malignancy) 4
- No intranodular flow on Doppler (benign feature) 1
- Symmetrical proportions (not taller-than-wide) 1
Understanding TI-RADS 3 Risk Level
- TI-RADS 3 carries a 1% to <10% risk of malignancy 1
- Research confirms no TR2 or TR3 nodules showed malignant cytology in validation studies 5
- The majority of TR4 nodules (78.9%) and TR5 nodules (64.6%) were benign on FNA, emphasizing that even higher-risk categories are predominantly benign 5
Important Clinical Considerations
Heterogeneous Echotexture Context
- The heterogeneous thyroid echotexture likely represents underlying thyroiditis (Hashimoto's or chronic lymphocytic thyroiditis) 1
- This background pattern does not independently increase malignancy risk of the nodules 1
- TSH measurement is particularly important in this context to assess thyroid function 1, 2
New Nodules Detected
- The report notes new nodules in both lobes compared to prior study 1
- New nodule development in the setting of heterogeneous thyroid is common with thyroiditis and does not automatically indicate malignancy 1
- All nodules should be measured and followed, but the same size thresholds apply 1, 2
Common Pitfalls to Avoid
- Do not perform FNA on nodules <1.5 cm with TI-RADS 3 classification, as this leads to unnecessary biopsies with high false-positive rates 1, 2, 5
- Do not skip thyroid function testing, as functional abnormalities may alter management 1, 2, 3
- Do not assume heterogeneous echotexture alone warrants biopsy—this is a common benign finding 1
- Be aware that FNA has a 5-10% false-negative rate, so maintain clinical vigilance during follow-up even with benign results 1
If Nodules Reach FNA Threshold
Should any nodule grow to ≥1.5 cm on follow-up 1, 2:
- Perform ultrasound-guided FNA with on-site cytopathology evaluation (preferred) 1
- Results will be reported using Bethesda classification (I-VI) 5
- If FNA shows benign cytology (Bethesda II), continue surveillance at 12-24 month intervals 1
- If indeterminate (Bethesda III-IV) or suspicious/malignant (Bethesda V-VI), refer for surgical consultation or molecular testing 1