| Literature DB >> 36120192 |
Juan Pesantez1, Carla Lituma1, Carla Valencia2, Jose Prieto3, Marco Cazorla4.
Abstract
Thyroid nodules are relatively prevalent in clinical practice; they are found by palpation in 3-7% of the general population and by ultrasonography (US) in roughly 50%. Image-guided nonsurgical procedures such as ethanol ablation (EA) or radiofrequency ablation (RFA) have been proposed for a selected group of patients as alternatives to traditional treatments. We present a case of a low-risk follicular variant of papillary thyroid cancer treated successfully with EA after examination and identification of the nodule as an ideal candidate for the treatment proposed. We highlight the efficacy of EA in this case, and how this contributes to the existing literature to continue proposing this as a viable treatment option.Entities:
Keywords: ethanol ablation; follicular tumor; papillary tumor; thyroid cancer; thyroid nodules
Year: 2022 PMID: 36120192 PMCID: PMC9467489 DOI: 10.7759/cureus.27960
Source DB: PubMed Journal: Cureus ISSN: 2168-8184
Figure 1Neck ultrasound showing the thyroid nodule with cystic features and microcalcifications
Figure 2Neck ultrasound after aspiration of fluid from the cystic space
Figure 3Reduction in volume of cystic space after ethanol injection
Figure 4Neck ultrasound showing a 4 x 6 mm (0.49 x 0.64 cm) thyroid cystic mass, compatible with shrinkage of the previously treated thyroid nodule
ATA 2009 risk stratification system with proposed modifications for structural disease recurrence in differentiated thyroid cancer
Adapted from Iñiguez-Ariza et al. [2].
ATA, American Thyroid Association; DM, distant metastases; EFVPTC, encapsulated follicular variant of papillary thyroid cancer; ETE, extrathyroidal extension; FTC, follicular thyroid cancer; Gross ETE, macroscopic invasion of tumor into the perithyroidal soft tissues; LN, lymph nodes; N0, no evidence of regional lymph node metastases; N1, metastases to regional node; PMC, papillary microcarcinoma; PTC, papillary thyroid carcinoma; RAI, radioactive iodine; WBS, whole body scan; WDFTC, well-differentiated follicular thyroid cancer.
| ATA low-risk | ATA intermediate risk | ATA high risk |
| PTC with all of the following: | Microscopic ETE | Gross ETE |
| No local or DM | RAI-avid metastatic foci in the neck on the first post-treatment WBS | Incomplete tumor resection |
| All macroscopic tumor has been resected | Aggressive cytotype (e.g., tall cell, hobnail variant, and columnar cell carcinoma) | Distant metastases |
| No tumor invasion of loco-regional tissues or structures | PTC with vascular invasion | Postoperative serum thyroglobulin suggestive of DM |
| No aggressive cytotype (e.g., tall cell, hobnail variant, and columnar cell carcinoma) | Clinical N1 or >5 pathologic N1 with all involved LN <3cm in the largest dimension | Pathologic N1 with any metastatic LN ≥3 cm in the largest dimension |
| If RAI was given, there are no RAI-avid metastatic foci outside the thyroid bed on the first post-treatment WBS | Multifocal PMC with ETE and BRAFV600E mutated (if known) | FTC with extensive vascular invasion (>4 foci of vascular invasion) |
| No vascular invasion | ||
| Clinical N0 or ≤5 pathologic N1 micro-metastases (<0.2 cm in largest dimension) | ||
| Intra-thyroidal EFVPTC | ||
| Intra-thyroidal WD-FTC with capsular invasion and no or minimal (<4 foci) vascular invasion | ||
| Intra-thyroidal PMC, unifocal or multifocal including BRAFV600E mutated (if known) |