Fluorescence-guided lymphatic mapping in patients with differentiated thyroid cancer
https://doi.org/10.24931/2413-9432-2026-15-2-4-8
Abstract
The role of prophylactic central neck dissection in patients with differentiated thyroid cancer without clinically evident lymph node involvement remains controversial despite its importance for staging and risk stratification. In this context, intraoperative lymphatic mapping may provide an opportunity to reduce the extent of surgical intervention.
The study included 125 patients with cN0 differentiated thyroid cancer who underwent thyroidectomy or hemityroidectomy. Central neck dissection was performed in 98 patients, while 27 patients underwent fluorescence-guided lymphatic mapping using indocyanine green with selective lymph node removal. The mean number of removed lymph nodes was significantly lower in the ICG group (3.67 vs 10.3; p < 0.001), while the rate of metastatic node detection did not differ between groups (33.3% vs 34.7%; p = 0.62). The incidence of transient hypoparathyroidism was comparable (14.8% vs 13.3%; p = 0.74), whereas permanent hypoparathyroidism was observed only in the central neck dissection group (17.3% vs 0%; p = 0.02). However, in the subgroup of patients undergoing thyroidectomy, no difference in transient hypoparathyroidism was found (15.5% vs 15.4%; p = 1.00). Permanent recurrent laryngeal nerve palsy occurred in 4.1% of patients in the control group and was not observed in the ICG group.
These findings suggest that fluorescence-guided lymphatic mapping allows selective lymph node removal with a reduced extent of dissection while maintaining a comparable rate of metastatic detection. The differences in postoperative complications appear to be primarily related to the extent of surgery. Further studies are required to evaluate the diagnostic accuracy and long-term outcomes of this approach.
About the Authors
F. P. VetshevRussian Federation
Moscow
K. K. Popov
Russian Federation
Moscow
S. P. Vetshev
Russian Federation
Moscow
L. I. Ippolotov
Russian Federation
Moscow
D. I. Gabaidze
Russian Federation
Moscow
S. S. Kharnas
Russian Federation
Moscow
M. B. Saliba
Russian Federation
Moscow
V. S. Tugusheva
Russian Federation
Moscow
References
1. Ringel M.D., Sosa J.A., Baloch Z. et al. 2025 American Thyroid Association Management Guidelines for Adult Patients with Differentiated Thyroid Cancer. Thyroid, 2025, vol. 35(8), pp. 841-985. doi:10.1177/10507256251363120
2. Sung H., Ferlay J., Siegel R.L. et al. Global Cancer Statistics 2020: CA Cancer J Clin, 2021, vol. 71(3), pp. 209–249. doi:10.3322/caac.21660
3. Pizzato M. et al. The epidemiological landscape of thyroid cancer worldwide. Lancet Diabetes Endocrinol, 2022, vol. 10(4), pp. 264–272. doi:10.1016/S2213-8587(22)00035-3
4. Kaprin A.D., Starinsky V.V., Shakhzadova A.O. The state of oncological care for the Russian population in 2023. Moscow: P.A. Herzen Moscow Institute of Medical Sciences – branch of the Federal State Budgetary Institution "NMITS of Radiology" of the Ministry of Health of the Russian Federation, 2024, pp. 248.
5. Lee J., Song Y., Soh E.Y. Prognostic Significance of the Number of Metastatic Lymph Nodes to Stratify the Risk of Recurrence. World J Surg, 2014, vol. 38(4), pp. 858–62. doi:10.1007/s00268-013-2345-6
6. Randolph G.W. et al. The prognostic significance of nodal metastases. Thyroid, 2012, vol. 22(11), pp. 1144–1152. doi:10.1089/thy.2012.0043
7. Miličić B. et al. Skip metastases in papillary thyroid carcinoma – prevalence, predictive and clinicopathological factors. Acta Clin Croat, 2020, vol. 59(1), pp. 123–131. doi:10.20471/acc.2020.59.s1.16.
8. Chen L., Wu Y.H., Lee C.H., Chen H.A., Loh E.W., Tam K.W. Prophylactic central neck dissection for papillary thyroid carcinoma with clinically uninvolved central neck lymph nodes: a systematic review and metaanalysis. World J Surg, 2018, vol. 42(9), pp. 2846–2857. doi:10.1007/s00268-018-4547-4.
9. Garau L.M., Rubello D., Ferretti A. et al. Sentinel lymph node biopsy in small papillary thyroid cancer. Endocrine, 2018, vol. 62(2), pp. 340–350. doi:10.1007/s12020-018-1658-5
10. Zhang X., Ning L., Liu D. et al. Clinical feasibility of imaging with indocyanine green combined with methylene blue for sentinel lymph node identification in papillary thyroid microcarcinoma. Medicine (Baltimore), 2019, vol. 98(36), pp. e16935. doi:10.1097/MD.0000000000016935
11. Sitges-Serra A., Ruiz S., Girvent M. et al. Outcome of protracted hypo-parathyroidism after total thyroidectomy. Br J Surg, 2010, vol. 97(11), pp. 1687–1695. doi:10.1002/bjs.7219
12. Fanaropoulou N.M., Chorti A., Markakis M., Papaioannou M., Michalopoulos A., Papavramidis T. The use of Indocyanine green in endocrine surgery of the neck: A systematic review. Medicine, 2019, vol. 98(10), pp. e14765. doi:10.1097/MD.0000000000014765
13. Di Marco A.N., Palazzo F.F. Near-infrared autofluorescence in thyroid and parathyroid surgery. Gland Surg, 2020, vol. 9(2), pp. 136–46. doi:10.21037/gs.2020.01.04
Review
For citations:
Vetshev F.P., Popov K.K., Vetshev S.P., Ippolotov L.I., Gabaidze D.I., Kharnas S.S., Saliba M.B., Tugusheva V.S. Fluorescence-guided lymphatic mapping in patients with differentiated thyroid cancer. Biomedical Photonics. 2026;15(2):4-8. https://doi.org/10.24931/2413-9432-2026-15-2-4-8
JATS XML


























