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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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Autores principales: Kure, Shoko, Ohashi, Ryuji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
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.
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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
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