Mixed medullary‑follicular thyroid carcinoma: A case report and literature review

Papillary thyroid cancer (PTC) and medullary thyroid cancer (MTC) originate from follicular and neuro-endocrine parafollicular C cells, respectively. PTC and MTC simultaneously exist in tumors containing both MTC and PTC features in a rare condition known as mixed medullary-follicular thyroid carcin...

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Veröffentlicht in:Oncology letters 2023-10, Vol.26 (4), p.1, Article 429
Hauptverfasser: Wang, Yonghui, Yin, Dandan, Ren, Guifang, Wang, Zhengjiang, Kong, Fanhua
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Sprache:eng
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Zusammenfassung:Papillary thyroid cancer (PTC) and medullary thyroid cancer (MTC) originate from follicular and neuro-endocrine parafollicular C cells, respectively. PTC and MTC simultaneously exist in tumors containing both MTC and PTC features in a rare condition known as mixed medullary-follicular thyroid carcinoma (MMFTC). In the present study, a 60-year-old female presented with a small mass on the left side of the neck. Ultrasonography indicated a hyperechoic nodule measuring ~11.9x9.7 [mm.sup.2] in the left lobe of the thyroid gland. The preoperative calcitonin serum value was elevated and total thyroidectomy and bilateral central compartment lymph node dissection was performed. Histological and immuno-histochemical analysis of the tumor demonstrated MMFTC. No metastasis was observed in lymph nodes isolated from the bilateral central compartment. Given the rarity of MMFTC, enhancing understanding and management of such tumors is crucial. Key words: medullary, follicular, papillary, thyroid cancer, case report
ISSN:1792-1074
1792-1082
DOI:10.3892/ol.2023.14015