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Thyroid Hürthle Cell Carcinoma: Clinical, Pathological, and Molecular Features
SIMPLE SUMMARY: Hürthle cell carcinoma (HCC) represents 3–4% of thyroid carcinoma cases. It is characterized by its large, granular and eosinophilic cytoplasm, due to an excessive number of mitochondria. Hürthle cells can be identified only after fine needle aspiration cytology biopsy or by histolog...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793513/ https://www.ncbi.nlm.nih.gov/pubmed/33374707 http://dx.doi.org/10.3390/cancers13010026 |
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author | Kure, Shoko Ohashi, Ryuji |
author_facet | Kure, Shoko Ohashi, Ryuji |
author_sort | Kure, Shoko |
collection | PubMed |
description | SIMPLE SUMMARY: Hürthle cell carcinoma (HCC) represents 3–4% of thyroid carcinoma cases. It is characterized by its large, granular and eosinophilic cytoplasm, due to an excessive number of mitochondria. Hürthle cells can be identified only after fine needle aspiration cytology biopsy or by histological diagnosis after the surgical operation. Published studies on HCC indicate its putative high aggressiveness. In this article, current knowledge of HCC focusing on clinical features, cytopathological features, genetic changes, as well as pitfalls in diagnosis are reviewed in order to improve clinical management. ABSTRACT: Hürthle cell carcinoma (HCC) represents 3–4% of thyroid carcinoma cases. It is considered to be more aggressive than non-oncocytic thyroid carcinomas. However, due to its rarity, the pathological characteristics and biological behavior of HCC remain to be elucidated. The Hürthle cell is characterized cytologically as a large cell with abundant eosinophilic, granular cytoplasm, and a large hyperchromatic nucleus with a prominent nucleolus. Cytoplasmic granularity is due to the presence of numerous mitochondria. These mitochondria display packed stacking cristae and are arranged in the center. HCC is more often observed in females in their 50–60s. Preoperative diagnosis is challenging, but indicators of malignancy are male, older age, tumor size > 4 cm, a solid nodule with an irregular border, or the presence of psammoma calcifications according to ultrasound. Thyroid lobectomy alone is sufficient treatment for small, unifocal, intrathyroidal carcinomas, or clinically detectable cervical nodal metastases, but total thyroidectomy is recommended for tumors larger than 4 cm. The effectiveness of radioactive iodine is still debated. Molecular changes involve cellular signaling pathways and mitochondria-related DNA. Current knowledge of Hürthle cell carcinoma, including clinical, pathological, and molecular features, with the aim of improving clinical management, is reviewed. |
format | Online Article Text |
id | pubmed-7793513 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77935132021-01-09 Thyroid Hürthle Cell Carcinoma: Clinical, Pathological, and Molecular Features Kure, Shoko Ohashi, Ryuji Cancers (Basel) Review SIMPLE SUMMARY: Hürthle cell carcinoma (HCC) represents 3–4% of thyroid carcinoma cases. It is characterized by its large, granular and eosinophilic cytoplasm, due to an excessive number of mitochondria. Hürthle cells can be identified only after fine needle aspiration cytology biopsy or by histological diagnosis after the surgical operation. Published studies on HCC indicate its putative high aggressiveness. In this article, current knowledge of HCC focusing on clinical features, cytopathological features, genetic changes, as well as pitfalls in diagnosis are reviewed in order to improve clinical management. ABSTRACT: Hürthle cell carcinoma (HCC) represents 3–4% of thyroid carcinoma cases. It is considered to be more aggressive than non-oncocytic thyroid carcinomas. However, due to its rarity, the pathological characteristics and biological behavior of HCC remain to be elucidated. The Hürthle cell is characterized cytologically as a large cell with abundant eosinophilic, granular cytoplasm, and a large hyperchromatic nucleus with a prominent nucleolus. Cytoplasmic granularity is due to the presence of numerous mitochondria. These mitochondria display packed stacking cristae and are arranged in the center. HCC is more often observed in females in their 50–60s. Preoperative diagnosis is challenging, but indicators of malignancy are male, older age, tumor size > 4 cm, a solid nodule with an irregular border, or the presence of psammoma calcifications according to ultrasound. Thyroid lobectomy alone is sufficient treatment for small, unifocal, intrathyroidal carcinomas, or clinically detectable cervical nodal metastases, but total thyroidectomy is recommended for tumors larger than 4 cm. The effectiveness of radioactive iodine is still debated. Molecular changes involve cellular signaling pathways and mitochondria-related DNA. Current knowledge of Hürthle cell carcinoma, including clinical, pathological, and molecular features, with the aim of improving clinical management, is reviewed. MDPI 2020-12-23 /pmc/articles/PMC7793513/ /pubmed/33374707 http://dx.doi.org/10.3390/cancers13010026 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Kure, Shoko Ohashi, Ryuji Thyroid Hürthle Cell Carcinoma: Clinical, Pathological, and Molecular Features |
title | Thyroid Hürthle Cell Carcinoma: Clinical, Pathological, and Molecular Features |
title_full | Thyroid Hürthle Cell Carcinoma: Clinical, Pathological, and Molecular Features |
title_fullStr | Thyroid Hürthle Cell Carcinoma: Clinical, Pathological, and Molecular Features |
title_full_unstemmed | Thyroid Hürthle Cell Carcinoma: Clinical, Pathological, and Molecular Features |
title_short | Thyroid Hürthle Cell Carcinoma: Clinical, Pathological, and Molecular Features |
title_sort | thyroid hürthle cell carcinoma: clinical, pathological, and molecular features |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7793513/ https://www.ncbi.nlm.nih.gov/pubmed/33374707 http://dx.doi.org/10.3390/cancers13010026 |
work_keys_str_mv | AT kureshoko thyroidhurthlecellcarcinomaclinicalpathologicalandmolecularfeatures AT ohashiryuji thyroidhurthlecellcarcinomaclinicalpathologicalandmolecularfeatures |