Current Oncology (Nov 2023)

Simultaneous Occurrence of Medullary Thyroid Carcinoma and Papillary Thyroid Carcinoma: A Case Series with Literature Review

  • Poupak Fallahi,
  • Armando Patrizio,
  • Giulio Stoppini,
  • Giusy Elia,
  • Francesca Ragusa,
  • Sabrina Rosaria Paparo,
  • Eugenia Balestri,
  • Valeria Mazzi,
  • Chiara Botrini,
  • Gilda Varricchi,
  • Salvatore Ulisse,
  • Marco Ghionzoli,
  • Alessandro Antonelli,
  • Silvia Martina Ferrari

DOI
https://doi.org/10.3390/curroncol30120745
Journal volume & issue
Vol. 30, no. 12
pp. 10237 – 10248

Abstract

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Background: Papillary thyroid carcinoma (PTC) is the most common type of differentiated TC, while medullary TC (MTC) accounts for 4%. The concomitant presence of PTC and MTC is rare. Methods: This is a retrospective, single-center observational study conducted over 16 years (2001–2017). The data were collected from the clinical records of patients who underwent total thyroidectomy at the Endocrine Unit-Department of Medicine of the University Hospital of Pisa, Italy. Results: Over 690 analyzed cases, 650 (94.2%) were exclusive DTC, 19 exclusive MTC (2.75%) and 5 PTC/MTC (0.7%). No case of mixed medullary/follicular TC or hereditary MTC (familial MTC/multiple endocrine neoplasia type 2) was found. Among the five PTC/MTC cases, there was a male prevalence (M:F = 3:2), and all PTC components were at stage I, whereas 40% of MTC were at stage I and III and 20% of MTC were at stage II; microPTC (mPTC) was prevalent (80%) and also microMTCs were frequent (40%); 60% of MTC patients recovered, while 40% of patients developed metastatic disease. The search for germline mutations of the RET gene resulted in being negative in all cases. Conclusions: The incidence of PTC/MTC has been increasing over the past 30 years. The etiology of PTC/MTC forms is still unknown, and although this simultaneous occurrence could be only a coincidence, we cannot exclude the hypothesis of a shared genetic origin.

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