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Updated: Sep 21, 2025

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Spontaneous Murine Model of Anaplastic Thyroid Cancer
Published on: February 3, 2023
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Synchronous Hürthle cell and medullary thyroid carcinomas.
Zhu Hui Yeap1, Sam Arman2, Grant Stenhouse3
1Otolaryngology, NHS Highland, Inverness, UK zhuhui.yeap@nhs.scot.
BMJ Case Reports
|May 31, 2022
Summary
This case report details the first documented instance of a collision tumor involving Hürthle cell carcinoma (HCC) and medullary thyroid carcinoma (MTC). It highlights the complex management of these rare thyroid cancers.
Area of Science:
- Endocrinology
- Oncology
- Pathology
Background:
- Hürthle cell carcinoma (HCC) and medullary thyroid carcinoma (MTC) are rare thyroid cancer subtypes, each comprising approximately 3% of all thyroid malignancies.
- Thyroid cancer management requires accurate histological subtyping for appropriate treatment strategies.
Observation:
- A septuagenarian woman with a history of multiple primary cancers presented with a neck mass.
- Initial surgery revealed two distinct malignant tumors: one HCC and one MTC.
- The patient later developed nodal metastasis of HCC and further intrathyroidal MTC with extranodal HCC extension.
Findings:
- This case represents the first reported instance of a collision tumor comprising both HCC and MTC.
- The patient required completion thyroidectomy and neck dissection due to disease progression.
Implications:
- Collision tumors of HCC and MTC are exceptionally rare, necessitating a high index of suspicion.
- Multidisciplinary team discussions are crucial for managing complex cases of rare thyroid cancers.
- Further research into the optimal management strategies for such collision tumors is warranted.
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