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Papillary Carcinoma: Cytology and Pathology

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Thyroid Cancer

Abstract

Papillary thyroid carcinoma (PTC) is the most common thyroid cancer and endocrine malignancy, constituting 75–85 % of the malignant thyroid lesions in regions where iodine-deficient goiter is no longer present (Rosai et al., Tumors of the thyroid gland. Washington, DC: Forces Institute of Pathology, 1992; Carcangiu et al., Pathol Annu 20(Pt 1):1–44, 1985). It represents most of the thyroid cancers that occur in children and young adults, whether idiopathic or related to radiation. A small proportion is familial (Moses et al., Thyroid ;21:367–371, 2011). Generally, PTCs grow slowly and therefore behave in an indolent fashion and spread mostly by lymphatic vessels to regional lymph nodes. Vascular invasion is rare in papillary thyroid carcinoma and metastases outside the confines of neck are rare (Mazzaferri, Semin Oncol 14:315–332, 1987). Both gross and microscopic features are varied, depending on cellularity, amount and type of stroma, architectural features and the presence or absence of cystic degeneration. Cytologic and pathologic features of the more common variants of PTC are described in this chapter and in Chap. 66 with clinical descriptions in Chap. 66.

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Baloch, Z.W., LiVolsi, V.A. (2016). Papillary Carcinoma: Cytology and Pathology. In: Wartofsky, L., Van Nostrand, D. (eds) Thyroid Cancer. Springer, New York, NY. https://doi.org/10.1007/978-1-4939-3314-3_32

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