<?xml version="1.0" encoding="UTF-8"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-10-18T23:53:59Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/10935" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/10935</identifier><datestamp>2026-10-18T21:13:10Z</datestamp><setSpec>openaire</setSpec><setSpec>driver</setSpec><setSpec>com_ebyu_10000</setSpec><setSpec>col_ebyu_10001</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:title>Columnar cell variant of papillary thyroid carcinoma in an adolescent: a comprehensive histopathological, immunohistochemical, and molecular analysis</dc:title><dc:creator>Issin, Gizem</dc:creator><dc:creator>Demir, Fatih</dc:creator><dc:creator>Cagatay, Diren Vuslat</dc:creator><dc:creator>Yilmaz, Ismail</dc:creator><dc:subject>columnar cell variant</dc:subject><dc:subject>pediatric endocrine neoplasms</dc:subject><dc:subject>pediatric thyroid carcinoma</dc:subject><dc:subject>rare thyroid tumor</dc:subject><dc:subject>thyroid carcinoma prognosis</dc:subject><dc:subject>Adolescent</dc:subject><dc:subject>Carcinoma, Papillary</dc:subject><dc:subject>Female</dc:subject><dc:subject>Humans</dc:subject><dc:subject>Immunohistochemistry</dc:subject><dc:subject>Thyroid Cancer, Papillary</dc:subject><dc:subject>Thyroid Neoplasms</dc:subject><dc:subject>case report</dc:subject><dc:subject>genetics</dc:subject><dc:subject>human</dc:subject><dc:subject>papillary carcinoma</dc:subject><dc:subject>pathology</dc:subject><dc:subject>procedures</dc:subject><dc:subject>thyroid papillary carcinoma</dc:subject><dc:subject>thyroid tumor</dc:subject><dc:description>The columnar cell variant (CCV) of papillary thyroid carcinoma (PTC) is a rare histological subtype with distinct morphological and immuno-histochemical (IHC) features, which can present diagnostic challenges. We report a case of a 13-year-old girl diagnosed with CCV of PTC (CCV–PTC) following a total thyroidectomy for a solitary thyroid nodule. Histopathological (HP) examination revealed aggressive features, including vascular invasion and extrathyroidal extension. However, no metastases or recurrences were observed during six years of follow-up. This case report provides a comprehensive analysis of a rare CCV–PTC in an adolescent, focusing on its HP, IHC, and molecular characteristics. It also discusses diagnostic pitfalls and differential diagnoses that should be considered. © 2025, Publishing House of the Romanian Academy. All rights reserved.</dc:description><dc:publisher>Publishing House of the Romanian Academy</dc:publisher><dc:date>2025</dc:date><dc:type>Article</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/10935</dc:identifier><dc:identifier>https://doi.org/10.47162/rjme.66.3.17</dc:identifier><dc:identifier>1220-0522</dc:identifier><dc:language>en</dc:language><dc:relation>Romanian Journal of Morphology and Embryology</dc:relation><dc:rights>info:eu-repo/semantics/openAccess</dc:rights><dc:type>info:eu-repo/semantics/article</dc:type><dc:identifier>https://ebyu-rdlopen.rawdatalibrary.net/tr/items/ebyu/10935</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>