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Histopathological features of condylar hyperplasia and condylar Osteochondroma: a comparison study

BACKGROUND: Both mandibular condylar hyperplasia and condylar osteochondroma can lead to maxillofacial skeletal asymmetry and malocclusion, although they exhibit different biological behavior. This study attempted to compare the histological features of mandibular condylar hyperplasia and condylar o...

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Autores principales: Yu, Jingshuang, Yang, Tong, Dai, Jiewen, Wang, Xudong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916444/
https://www.ncbi.nlm.nih.gov/pubmed/31842965
http://dx.doi.org/10.1186/s13023-019-1272-5
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author Yu, Jingshuang
Yang, Tong
Dai, Jiewen
Wang, Xudong
author_facet Yu, Jingshuang
Yang, Tong
Dai, Jiewen
Wang, Xudong
author_sort Yu, Jingshuang
collection PubMed
description BACKGROUND: Both mandibular condylar hyperplasia and condylar osteochondroma can lead to maxillofacial skeletal asymmetry and malocclusion, although they exhibit different biological behavior. This study attempted to compare the histological features of mandibular condylar hyperplasia and condylar osteochondroma using hematoxylin-and-eosin (H&E) staining, and immunohistochemistry staining of PCNA and EXT1 with quantitative analysis method. RESULTS: The H&E staining showed that condylar hyperplasia and condylar osteochondroma could be divided into four histological types and exhibited features of different endochondral ossification stages. There was evidence of a thicker cartilage cap in condylar osteochondroma as compared condylar hyperplasia (P = 0.018). The percentage of bone formation in condylar osteochondroma was larger than was found in condylar hyperplasia (P = 0.04). Immunohistochemical staining showed that PCNA was mainly located in the undifferentiated mesenchymal layer and the hypertrophic cartilage layer, and there were more PCNA positive cells in the condylar osteochondroma (P = 0.007). EXT1 was mainly expressed in the cartilage layer, and there was also a higher positive rate of EXT1 in condylar osteochondroma (P = 0.0366). The thicker cartilage cap, higher bone formation rate and higher PCNA positive rate indicated a higher rate of proliferative activity in condylar osteochondroma. The more significant positive rate of EXT1 in condylar osteochondroma implied differential biological characteristic as compared to condylar hyperplasia. CONCLUSIONS: These features might be useful in histopathologically distinguishing condylar hyperplasia and osteochondroma.
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spelling pubmed-69164442019-12-20 Histopathological features of condylar hyperplasia and condylar Osteochondroma: a comparison study Yu, Jingshuang Yang, Tong Dai, Jiewen Wang, Xudong Orphanet J Rare Dis Research BACKGROUND: Both mandibular condylar hyperplasia and condylar osteochondroma can lead to maxillofacial skeletal asymmetry and malocclusion, although they exhibit different biological behavior. This study attempted to compare the histological features of mandibular condylar hyperplasia and condylar osteochondroma using hematoxylin-and-eosin (H&E) staining, and immunohistochemistry staining of PCNA and EXT1 with quantitative analysis method. RESULTS: The H&E staining showed that condylar hyperplasia and condylar osteochondroma could be divided into four histological types and exhibited features of different endochondral ossification stages. There was evidence of a thicker cartilage cap in condylar osteochondroma as compared condylar hyperplasia (P = 0.018). The percentage of bone formation in condylar osteochondroma was larger than was found in condylar hyperplasia (P = 0.04). Immunohistochemical staining showed that PCNA was mainly located in the undifferentiated mesenchymal layer and the hypertrophic cartilage layer, and there were more PCNA positive cells in the condylar osteochondroma (P = 0.007). EXT1 was mainly expressed in the cartilage layer, and there was also a higher positive rate of EXT1 in condylar osteochondroma (P = 0.0366). The thicker cartilage cap, higher bone formation rate and higher PCNA positive rate indicated a higher rate of proliferative activity in condylar osteochondroma. The more significant positive rate of EXT1 in condylar osteochondroma implied differential biological characteristic as compared to condylar hyperplasia. CONCLUSIONS: These features might be useful in histopathologically distinguishing condylar hyperplasia and osteochondroma. BioMed Central 2019-12-16 /pmc/articles/PMC6916444/ /pubmed/31842965 http://dx.doi.org/10.1186/s13023-019-1272-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Yu, Jingshuang
Yang, Tong
Dai, Jiewen
Wang, Xudong
Histopathological features of condylar hyperplasia and condylar Osteochondroma: a comparison study
title Histopathological features of condylar hyperplasia and condylar Osteochondroma: a comparison study
title_full Histopathological features of condylar hyperplasia and condylar Osteochondroma: a comparison study
title_fullStr Histopathological features of condylar hyperplasia and condylar Osteochondroma: a comparison study
title_full_unstemmed Histopathological features of condylar hyperplasia and condylar Osteochondroma: a comparison study
title_short Histopathological features of condylar hyperplasia and condylar Osteochondroma: a comparison study
title_sort histopathological features of condylar hyperplasia and condylar osteochondroma: a comparison study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916444/
https://www.ncbi.nlm.nih.gov/pubmed/31842965
http://dx.doi.org/10.1186/s13023-019-1272-5
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