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Papillary Carcinoma

Clinical Aspects

  • Chapter
Thyroid Cancer

Abstract

Papillary thyroid carcinoma (PTC) is a cancer of the thyroid follicular epithelium; like follicular carcinoma, it is the more highly differentiated of all of the classes of thyroid malignancy. The biological behavior of PTC varies widely, from small (<1.0 cm) tumors found at autopsy with surprisingly high frequency that show little evidence of invasion, to rapidly growing, locally invasive tumors that may be resistant to radioiodine therapy, eventually metastasizing and can cause death. To date, it has not been possible in a given patient to predict which course the tumor may take until several years, or even decades, of follow-up have elapsed. Fortunately, the overwhelming majority of tumors less than 1.5 cm in diameter tend to behave in a more biologically benign manner and can be completely cured with definitive therapy. This reflects the importance of tumor size on prognosis and risk of recurrence or death. Although PTC tends to affect women more often than men (ñ2:1), the risk of cancer in thyroid nodules in men is equally, if not more, significant because of the much lower frequency of any type of thyroid disease in men. This chapter deals with several clinical aspects of these tumors and descriptions of pathology and management appear in the immediate chapters that follow.

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Wartofsky, L. (2006). Papillary Carcinoma. In: Wartofsky, L., Van Nostrand, D. (eds) Thyroid Cancer. Humana Press. https://doi.org/10.1007/978-1-59259-995-0_23

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