Abstract
The optimal surgical management of low-risk papillary thyroid cancer (PTC) has remained a controversial topic for many decades. Recent guidelines propose that both thyroid lobectomy and total thyroidectomy for low-risk PTC may be appropriate and safe, based on available clinical information and patient preferences. Approximately 7–10% of patients with PTC have a family history of thyroid cancer. Some investigators have suggested familial PTC is more aggressive, with advanced disease at presentation and a higher risk of recurrence. In this chapter, we discuss the options available for the surgical management of patients with low-risk PTC and a family history of differentiated thyroid cancer. While there is reportedly no difference in survival among patients with low-risk PTC treated with thyroid lobectomy versus total thyroidectomy, patients with familial PTC (three or more first-degree relatives affected) may benefit from total thyroidectomy, given the higher risk of multicentricity and bilateral tumors, and risk of recurrence. Alternatively, for patients diagnosed with low-risk PTC on screening, with only two first-degree relatives affected with differentiated thyroid cancer, a strong desire to avoid thyroid hormone replacement and commitment to participate in an active surveillance program, a thyroid lobectomy is a reasonable treatment approach.
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Alobuia, W., Kebebew, E. (2023). Management of Low-risk Papillary Thyroid Cancer in a Patient with Familial Non-Medullary Thyroid Cancer. In: Roman, S.A., Shen, W.T., Sosa, J.A. (eds) Controversies in Thyroid Nodules and Differentiated Thyroid Cancer. Springer, Cham. https://doi.org/10.1007/978-3-031-37135-6_7
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