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Updated: Feb 1, 2026

Author Spotlight: Integrating Ultrasound Imaging with Biochemical Markers for Thyroid Disease Diagnosis
Published on: February 9, 2024
HATRICK-Synchronous Triple Primary Tumors of Thyroid
A P Roshini1, Rakesh Ramesh2, T Rajalakshmi3
11St. John's Medical College and Hospital, Bengaluru, Karnataka India.
A rare case of triple thyroid tumors, including papillary carcinoma thyroid and medullary carcinoma thyroid, was found in a young woman. This simultaneous occurrence of multiple primary cancers (MPC) in the thyroid is exceptionally uncommon.
Area of Science:
- Endocrinology
- Oncology
- Pathology
Background:
- Multiple primary cancer (MPC) involves diagnosing two or more distinct cancers in one patient, with an incidence of 1.8%. Synchronous tumors are defined as two or more primary tumors diagnosed within six months.
- Thyroid nodules are common, but the concurrent presence of multiple distinct thyroid malignancies is rare.
Observation:
- A 27-year-old female presented with a year-long, painless, progressive right-sided neck swelling.
- Initial ultrasound revealed a hypoechoic solid nodule on the right thyroid lobe, with the left lobe appearing normal.
- Fine-needle aspiration cytology (FNAC) suggested an adenomatous colloid nodule (Bethesda II).
Findings:
- Histopathological examination of the right hemithyroidectomy specimen unexpectedly revealed three distinct tumors: a not-otherwise-specified (NOS) tumor, papillary carcinoma thyroid (PTC), and medullary carcinoma thyroid.
- Immunohistochemistry (IHC) confirmed the presence of medullary carcinoma thyroid through positive staining for synaptophysin, CEA, and chromogranin.
Implications:
- This case represents an extremely rare instance of concurrent triple thyroid tumors (NOS, PTC, and medullary carcinoma) in a single patient.
- The simultaneous occurrence highlights the complexity of thyroid cancer diagnosis and the potential for multiple primary malignancies.
- Further investigation into the genetic and etiological factors contributing to such rare multifocal thyroid neoplasms may be warranted.
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