Warthin-Like Variant of Papillary Thyroid Carcinoma: A Rare Case in an Adolescent Female with Diagnostic and Clinical Insights

Abstract The Warthin-like subtype of papillary thyroid carcinoma (WL-PTC) represents a rare morphological variant, often linked with Hashimoto’s thyroiditis. Characterized by oncocytic epithelial cells forming papillae amid dense lymphoplasmacytic infiltration, this variant typically presents in adult women. Due to imaging and cytological overlaps with classical PTC, preoperative diagnosis can be intricate. This report details an exceptional case involving an 18-year-old female with a left thyroid lobe nodule. Cytological assessment indicated PTC, later confirmed as WL-PTC following histological evaluation post-thyroidectomy. The tumor exhibited defining oncocytic and nuclear features amid prominent lymphoid stroma. Recognizing such rare variants is crucial to avoid misdiagnosis and to tailor appropriate management, especially given their generally favorable prognosis.

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Publication Details

Journal
Journal of Microscopy and Ultrastructure
Published
2026-06-26
DOI
https://doi.org/10.4103/jmau.jmau_50_25
Primary Topic
Thyroid Cancer Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00
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article

Warthin-Like Variant of Papillary Thyroid Carcinoma: A Rare Case in an Adolescent Female with Diagnostic and Clinical Insights

Tanvi Jha, Kriti Roy, Neha A. Singh
Journal of Microscopy and Ultrastructure
Thyroid Cancer Diagnosis and Treatment
article

Warthin-Like Variant of Papillary Thyroid Carcinoma: A Rare Case in an Adolescent Female with Diagnostic and Clinical Insights

Tanvi Jha, Kriti Roy, Neha A. Singh
article en

Abstract

Abstract The Warthin-like subtype of papillary thyroid carcinoma (WL-PTC) represents a rare morphological variant, often linked with Hashimoto’s thyroiditis. Characterized by oncocytic epithelial cells forming papillae amid dense lymphoplasmacytic infiltration, this variant typically presents in adult women. Due to imaging and cytological overlaps with classical PTC, preoperative diagnosis can be intricate. This report details an exceptional case involving an 18-year-old female with a left thyroid lobe nodule. Cytological assessment indicated PTC, later confirmed as WL-PTC following histological evaluation post-thyroidectomy. The tumor exhibited defining oncocytic and nuclear features amid prominent lymphoid stroma. Recognizing such rare variants is crucial to avoid misdiagnosis and to tailor appropriate management, especially given their generally favorable prognosis.

Journal of Microscopy and Ultrastructure
Atal Bihari Vajpayee Institute of Medical Sciences and Dr. Ram Manohar Lohia Hospital (IN), Institute of Medical Sciences (IN)
Good health and well-being
Openalex Percentile: Top 7%
Thyroid Cancer Diagnosis and Treatment
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