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Primary small cell thyroid carcinoma combined with poorly differentiated thyroid carcinoma, evidence for a common origin: A case report

  • Kyoung Min Kim
  • , Ae Ri Ahn
  • , Yong Tae Hong
  • , Myoung Ja Chung*
  • *Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

Abstract

Primary small cell thyroid carcinomas are extremely rare and there is still debate about their classifi‑ cation as a distinct disease entity. The present case report reports a small cell carcinoma (SCC) combined with poorly differentiated thyroid carcinoma (PDTC) in a 34 year old man. The tumor consisted of ~80% PDTC and ~20% SCC. The PDTC component was positive for cytokeratin and thyroid transcription factor‑1 (TTF‑1), and negative for calcitonin, chromogranin and synaptophysin. The SCC component was positive for synaptophysin and CD56, and negative for calci‑ tonin, chromogranin and TTF‑1. Seven months after thyroid surgery, two new lung nodules were detected. Histologically and immunohistochemically, the lung tumors were similar to the SCC component of the thyroid carcinoma. The mutational status of cancer‑related genes was assessed using targeted next‑generation sequencing in both the thyroid and lung, which identified similar genetic alterations. The histogenesis of SCC was evaluated through NGS analysis of the two cancer components.

Original languageEnglish
Article number233
JournalOncology Letters
Volume25
Issue number6
DOIs
StatePublished - 2023.06

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • next generation sequencing
  • poorly differentiated carcinoma
  • small cell carcinoma
  • thyroid

Quacquarelli Symonds(QS) Subject Topics

  • Medicine
  • Biological Sciences

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