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Cytomorphologic features distinguishing Bethesda category IV thyroid lesions from parathyroid

BACKGROUND: Thyroid follicular cells share similar cytomorphological features with parathyroid. Without a clinical suspicion, the distinction between a thyroid neoplasm and an intrathyroidal parathyroid can be challenging. The aim of this study was to assess the distinguishing cytomorphological feat...

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Autores principales: Sung, Simon, Saqi, Anjali, Margolskee, Elizabeth M., Crapanzano, John P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430501/
https://www.ncbi.nlm.nih.gov/pubmed/28567111
http://dx.doi.org/10.4103/1742-6413.205313
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author Sung, Simon
Saqi, Anjali
Margolskee, Elizabeth M.
Crapanzano, John P.
author_facet Sung, Simon
Saqi, Anjali
Margolskee, Elizabeth M.
Crapanzano, John P.
author_sort Sung, Simon
collection PubMed
description BACKGROUND: Thyroid follicular cells share similar cytomorphological features with parathyroid. Without a clinical suspicion, the distinction between a thyroid neoplasm and an intrathyroidal parathyroid can be challenging. The aim of this study was to assess the distinguishing cytomorphological features of parathyroid (including intrathyroidal) and Bethesda category IV (Beth-IV) thyroid follicular lesions, which carry a 15%–30% risk of malignancy and are often followed up with surgical resection. METHODS: A search was performed to identify “parathyroid” diagnoses in parathyroid/thyroid-designated fine-needle aspirations (FNAs) and Beth-IV thyroid FNAs (follicular and Hurthle cell), all with diagnostic confirmation through surgical pathology, immunocytochemical stains, Afirma(®) analysis, and/or clinical correlation. Unique cytomorphologic features were scored (0-3) or noted as present versus absent. Statistical analysis was performed using R 3.3.1 software. RESULTS: We identified five FNA cases with clinical suspicion of parathyroid neoplasm, hyperthyroidism, or thyroid lesion that had an eventual final diagnosis of the parathyroid lesion (all female; age 20–69 years) and 12 Beth-IV diagnoses (11 female, 1 male; age 13–64 years). The following cytomorphologic features are useful distinguishing features (P value): overall pattern (0.001), single cells (0.001), cell size compared to red blood cell (0.01), nuclear irregularity (0.001), presence of nucleoli (0.001), nuclear-to-cytoplasmic ratio (0.007), and nuclear chromatin quality (0.028). CONCLUSIONS: There are cytomorphologic features that distinguish Beth-IV thyroid lesions and (intrathyroidal) parathyroid. These features can aid in rendering correct diagnoses and appropriate management.
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spelling pubmed-54305012017-05-31 Cytomorphologic features distinguishing Bethesda category IV thyroid lesions from parathyroid Sung, Simon Saqi, Anjali Margolskee, Elizabeth M. Crapanzano, John P. Cytojournal Research Article BACKGROUND: Thyroid follicular cells share similar cytomorphological features with parathyroid. Without a clinical suspicion, the distinction between a thyroid neoplasm and an intrathyroidal parathyroid can be challenging. The aim of this study was to assess the distinguishing cytomorphological features of parathyroid (including intrathyroidal) and Bethesda category IV (Beth-IV) thyroid follicular lesions, which carry a 15%–30% risk of malignancy and are often followed up with surgical resection. METHODS: A search was performed to identify “parathyroid” diagnoses in parathyroid/thyroid-designated fine-needle aspirations (FNAs) and Beth-IV thyroid FNAs (follicular and Hurthle cell), all with diagnostic confirmation through surgical pathology, immunocytochemical stains, Afirma(®) analysis, and/or clinical correlation. Unique cytomorphologic features were scored (0-3) or noted as present versus absent. Statistical analysis was performed using R 3.3.1 software. RESULTS: We identified five FNA cases with clinical suspicion of parathyroid neoplasm, hyperthyroidism, or thyroid lesion that had an eventual final diagnosis of the parathyroid lesion (all female; age 20–69 years) and 12 Beth-IV diagnoses (11 female, 1 male; age 13–64 years). The following cytomorphologic features are useful distinguishing features (P value): overall pattern (0.001), single cells (0.001), cell size compared to red blood cell (0.01), nuclear irregularity (0.001), presence of nucleoli (0.001), nuclear-to-cytoplasmic ratio (0.007), and nuclear chromatin quality (0.028). CONCLUSIONS: There are cytomorphologic features that distinguish Beth-IV thyroid lesions and (intrathyroidal) parathyroid. These features can aid in rendering correct diagnoses and appropriate management. Medknow Publications & Media Pvt Ltd 2017-04-28 /pmc/articles/PMC5430501/ /pubmed/28567111 http://dx.doi.org/10.4103/1742-6413.205313 Text en Copyright: © 2017 Sung, et al.; Licensee Cytopathology Foundation Inc. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Research Article
Sung, Simon
Saqi, Anjali
Margolskee, Elizabeth M.
Crapanzano, John P.
Cytomorphologic features distinguishing Bethesda category IV thyroid lesions from parathyroid
title Cytomorphologic features distinguishing Bethesda category IV thyroid lesions from parathyroid
title_full Cytomorphologic features distinguishing Bethesda category IV thyroid lesions from parathyroid
title_fullStr Cytomorphologic features distinguishing Bethesda category IV thyroid lesions from parathyroid
title_full_unstemmed Cytomorphologic features distinguishing Bethesda category IV thyroid lesions from parathyroid
title_short Cytomorphologic features distinguishing Bethesda category IV thyroid lesions from parathyroid
title_sort cytomorphologic features distinguishing bethesda category iv thyroid lesions from parathyroid
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430501/
https://www.ncbi.nlm.nih.gov/pubmed/28567111
http://dx.doi.org/10.4103/1742-6413.205313
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