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Hyalinizing trabecular tumor of the thyroid: a case report
P Caraci1, A Fulcheri, C Ondolo
1Section of Internal Medicine, San Luigi Hospital, regione Gonzole 10, Orbassano (Torino) 10043, Italy.
Head and Neck Pathology
|July 2, 2011
Summary
Hyalinizing trabecular tumor (HTT) is a rare thyroid neoplasm. Management should be conservative, focusing on surgical options and annual follow-up due to its generally benign nature.
Area of Science:
- Endocrinology
- Oncology
- Pathology
Background:
- Hyalinizing trabecular tumor (HTT) is a rare thyroid neoplasm of follicular origin.
- First described by Carney in 1987, HTT exhibits unique nuclear, architectural, histochemical, and immunohistochemical characteristics.
Observation:
- A case of HTT in a 69-year-old woman with multinodular goiter is presented.
- Nonspecific clinical and ultrasonographic features led to an indeterminate fine needle aspiration biopsy (FNAB) diagnosis (THY-3).
- Histologic diagnosis of HTT was confirmed post-total thyroidectomy.
Findings:
- The study discusses the clinical and diagnostic approach to HTT, emphasizing the role of FNAB.
- Pathologic features and differential diagnoses of HTT are reviewed.
- Total thyroidectomy or hemithyroidectomy are considered adequate treatments; radioiodine ablation is not standard.
Implications:
- HTT is generally considered a benign neoplasm or one with extremely low malignant potential.
- Conservative management, including precautionary annual follow-up, is recommended after diagnosis.
- This approach aims to exclude the rare possibility of recurrence.
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