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Cytology and Pathology: Pitfalls and Challenges

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Abstract

This chapter reviews the morphological features of thyroid C-cell proliferations with a focus on identifying the potential pitfalls in the diagnosis of these important disorders. The most important component of making the diagnosis of medullary thyroid carcinoma is to consider it in the differential diagnosis. The spectrum of parafollicular C-cell proliferations includes C-cell hyperplasia, medullary thyroid carcinoma, and mixed medullary and follicular epithelial tumors. Various histologic variants of medullary thyroid carcinoma can pose diagnostic challenges; however, with the application of immunohistochemistry, C-cell proliferations can be identified. The important markers include those of neuroendocrine differentiation, synaptophysin and chromogranin, and their specific peptide products, calcitonin and carcinoembryonic antigen. Since 25 % of medullary thyroid carcinomas are inherited, pathologists can provide insights into those that warrant genetic testing by performing C-cell mapping that determines whether there is associated C-cell hyperplasia and whether its growth pattern (nodular vs. linear) suggests genetic predisposition. Molecular markers can be applied to predict appropriate therapy, and immunohistochemistry can prove unusual hormone production associated with various clinical syndromes. Novel prognostic markers are being identified, but the accurate identification of angioinvasion is an important feature that has been shown to be the most reliable predictor of disease recurrence and death.

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Asa, S.L., Mete, O. (2016). Cytology and Pathology: Pitfalls and Challenges. In: Wang, T., Evans, D. (eds) Medullary Thyroid Cancer. Springer, Cham. https://doi.org/10.1007/978-3-319-39412-1_4

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