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ArticleAACE endocrinology and diabetes

Coexistence of Hyalinizing Trabecular Tumor and Papillary Thyroid Carcinoma: A Diagnostic Challenge.

Mubashirah S Charolia, Alka Rani, Aisha Hassan Memon, Shayan Anwar, Saira Fatima

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Article in AACE endocrinology and diabetes. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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5 authors.

Mubashirah S CharoliaMedical College, Aga Khan University, Karachi, Pakistan.
Alka RaniDepartment of Pathology and Laboratory Medicine, Aga Khan University, Karachi, Pakistan.
Aisha Hassan MemonDepartment of Pathology and Laboratory Medicine, Aga Khan University, Karachi, Pakistan.
Shayan AnwarDepartment of Radiology, Aga Khan University, Karachi, Pakistan.
Saira FatimaDepartment of Pathology and Laboratory Medicine, Aga Khan University, Karachi, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Objective: Hyalinizing trabecular tumor (HTT) of the thyroid is an uncommon follicular cell-derived neoplasm. Histologically, it shares several nuclear features with papillary thyroid carcinoma (PTC), such as nuclear grooves and pseudoinclusions, making accurate diagnosis challenging, particularly in cytology. Coexistence of HTT and PTC within the same thyroid gland is exceptionally rare and can further complicate clinical interpretation. Case Report: A 54-year-old woman presented with a gradually enlarging anterior neck swelling. Ultrasound revealed 2 nodules in the right thyroid lobe with differing echogenic features. Fine-needle aspiration cytology was reported as Bethesda Category III (Atypia of Undetermined Significance). A right lobectomy was performed for definitive diagnosis. Histopathology revealed 2 distinct lesions: a 1.2 cm hyalinizing trabecular tumor showing trabecular architecture, hyalinized stroma, CD56 positivity, and characteristic membranous Ki-67 staining; and an incidental 0.1 cm papillary thyroid carcinoma exhibiting fibrovascular cores with nuclear clearing and grooves, CK19 positivity, and CD56 loss. No capsular, vascular, or extrathyroidal invasion was identified. The patient recovered uneventfully and remains disease-free after 2.5 years of follow-up. Discussion: The coexistence of HTT and PTC within the same thyroid gland is a rare but documented phenomenon, reported in only a few cases worldwide. The morphologic overlap between HTT and PTC frequently leads to diagnostic uncertainty in cytology. Immunohistochemistry and, when available, molecular testing for GLIS1/GLIS3 rearrangements provide essential diagnostic clarity. Conclusion: This case underscores the importance of integrating cytologic, histopathologic, and molecular features when evaluating thyroid nodules with overlapping characteristics. Recognition of this rare coexistence prevents misclassification and unnecessary aggressive management, ensuring accurate diagnosis and optimal patient outcomes.

Indexed as

case reportfine-needle aspirationhyalinizing trabecular tumorimmunohistochemistrypapillary thyroid carcinomathyroid neoplasms

Identifiers

PMID42221404
PMCPMC13221926

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