Sunil V. Jagtap Professor, Department of Pathology, Krishna Vishwa Vidyapeeth, Krishna Institute of Medical Sciences, Karad 415539, Maharashtra, India
Shubham S Jagtap Resident, Department of Medicine, Krishna Vishwa Vidyapeeth, Krishna Institute of Medical Sciences, Karad 415539, Maharashtra, India
Maanasi R Bhade Resident, Department of Pathology,Krishna Vishwa Vidyapeeth, Krishna Institute of Medical Sciences, Karad 415539, Maharashtra, India
Drashti Maradiya Resident, Department of Pathology, Krishna Vishwa Vidyapeeth, Krishna Institute of Medical Sciences, Karad 415539, Maharashtra, India
Dhwani Mavani Resident, Department of Pathology, Krishna Vishwa Vidyapeeth, Krishna Institute of Medical Sciences, Karad 415539, Maharashtra, India
Abhilasha S Jadhav Tutor, Department of Pathology, Krishna Vishwa Vidyapeeth, Krishna Institute of Medical Sciences, Karad 415539, Maharashtra, India
Address for correspondence: Sunil V. Jagtap, Professor, Department of Pathology, Krishna Vishwa Vidyapeeth, Krishna Institute of Medical Sciences, Karad 415539, Maharashtra, India E-mail: drsvjagtap@gmail.com
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Sunil V. Jagtap, Shubham S Jagtap, Maanasi R Bhade et al. Oncocytic (Hurthle Cell )Adenoma: A Rare, Benign tumor of thyroidcase report and Review of literature. Ind Jr of Path: Res and Practice 2025;14(1)21-25.
Timeline
Received : February 01, 2025
Accepted : March 05, 2025
Published : April 30, 2025
Abstract
Oncocytic (Hurthle cell) adenoma is A Rare, Benign tumor of the thyroid gland. A 66-yearold woman presented with midline painless neck swelling over the past 3 months. The swelling moves up and down with her swallowing. On examination the swelling measured about 3x3x2.4 cm in size, in the right lobe of the thyroid gland. There was no symptoms of palpitation, hoarseness, or any pressure related signs. There was no family history of thyroid cancer. The ultrasonography showed right thyroid well circumscribed, heterogenous nodular mass lesion measuring 3.0x3.6 cm. Fine niddle aspiration cytology showed moderately cellular smears composed predominantly of Hürthle cells with abundant fine granular cytoplasm. Cellular atypia was noted. On cytology reported as suspicious for a follicular neoplasm with Hürthle cell type. Our patient underwent simple lobectomy. On histopathological findings reported as Oncocytic cell adenoma thyroid. Patient showed a good postoperative prognosis. This article presents a case of Oncocytic/Hurthle cell adenoma of the thyroid gland with a review of literature.
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Data Sharing Statement
There are no additional data available. All raw data and code are available upon request.
Funding
This research received no funding.
Author Contributions
All authors contributed significantly to the work and approve its publication.
Ethics Declaration
This article does not involve any human or animal subjects, and therefore does not require ethics approval.
Acknowledgements
We would like to express our gratitude to the patients, their families, and all those who have contributed to this study.
Conflicts of Interest
No conflicts of interest in this work.
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Cite this article
Sunil V. Jagtap, Shubham S Jagtap, Maanasi R Bhade et al. Oncocytic (Hurthle Cell )Adenoma: A Rare, Benign tumor of thyroidcase report and Review of literature. Ind Jr of Path: Res and Practice 2025;14(1)21-25.
This license
enables reusers to distribute, remix, adapt, and build upon the material in any
medium or format for noncommercial purposes only, and only so long as
attribution is given to the creator.
This license
enables reusers to distribute, remix, adapt, and build upon the material in any
medium or format for noncommercial purposes only, and only so long as
attribution is given to the creator.