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p63 as a prognostic marker for giant cell tumor of bone

BACKGROUND AND PURPOSE: Giant cell tumor of bone (GCT) is sometimes difficult to distinguish from other giant-cell-rich tumors such as chondroblastoma (CHB) and aneurysmal bone cyst (ABC). The usefulness of p63 as a diagnostic marker for GCT is controversial. While there have been no reports about p...

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Autores principales: Yanagisawa, Michiro, kakizaki, Hiroshi, Okada, Kyoji, Torigoe, Tomoaki, Kusumi, Tomomi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Informa Healthcare 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3572666/
https://www.ncbi.nlm.nih.gov/pubmed/23033898
http://dx.doi.org/10.3109/03009734.2012.724731
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author Yanagisawa, Michiro
kakizaki, Hiroshi
Okada, Kyoji
Torigoe, Tomoaki
Kusumi, Tomomi
author_facet Yanagisawa, Michiro
kakizaki, Hiroshi
Okada, Kyoji
Torigoe, Tomoaki
Kusumi, Tomomi
author_sort Yanagisawa, Michiro
collection PubMed
description BACKGROUND AND PURPOSE: Giant cell tumor of bone (GCT) is sometimes difficult to distinguish from other giant-cell-rich tumors such as chondroblastoma (CHB) and aneurysmal bone cyst (ABC). The usefulness of p63 as a diagnostic marker for GCT is controversial. While there have been no reports about p63 as a prognostic marker for local recurrence, various p63-positive rates in GCT have been reported. The purpose of this study was to investigate retrospectively whether p63 is useful as a diagnostic marker and/or a prognostic marker for local recurrence of GCT. METHODS: This study included 36 patients diagnosed with either GCT (n = 16), CHB (n = 9), ABC (n = 7), or non-ossifying fibroma (NOF) (n = 4). p63 immunostaining was performed for all specimens. The mean p63-positive rate was compared with the four diseases and between the recurrent and non-recurrent cases of GCT. RESULTS: Although the mean p63-positive rate for GCT (36.3%) was statistically higher than that of all other diseases examined (CHB: 15.2%; ABC: 5.8%; NOF: 3.4%), p63 was not specific for GCT. The mean p63-positive rate for recurrent GCT cases (73.6%) was statistically higher than that for non-recurrent cases (29.1%). CONCLUSION: In the diagnosis of GCT, p63 is a useful but not a conclusive marker. However, p63 did appear to indicate the biological aggressiveness of GCT. Therefore, p63 may help surgeons to estimate the risk of recurrence after surgery and help them to choose the best treatment for each GCT case.
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spelling pubmed-35726662013-03-15 p63 as a prognostic marker for giant cell tumor of bone Yanagisawa, Michiro kakizaki, Hiroshi Okada, Kyoji Torigoe, Tomoaki Kusumi, Tomomi Ups J Med Sci Original Article BACKGROUND AND PURPOSE: Giant cell tumor of bone (GCT) is sometimes difficult to distinguish from other giant-cell-rich tumors such as chondroblastoma (CHB) and aneurysmal bone cyst (ABC). The usefulness of p63 as a diagnostic marker for GCT is controversial. While there have been no reports about p63 as a prognostic marker for local recurrence, various p63-positive rates in GCT have been reported. The purpose of this study was to investigate retrospectively whether p63 is useful as a diagnostic marker and/or a prognostic marker for local recurrence of GCT. METHODS: This study included 36 patients diagnosed with either GCT (n = 16), CHB (n = 9), ABC (n = 7), or non-ossifying fibroma (NOF) (n = 4). p63 immunostaining was performed for all specimens. The mean p63-positive rate was compared with the four diseases and between the recurrent and non-recurrent cases of GCT. RESULTS: Although the mean p63-positive rate for GCT (36.3%) was statistically higher than that of all other diseases examined (CHB: 15.2%; ABC: 5.8%; NOF: 3.4%), p63 was not specific for GCT. The mean p63-positive rate for recurrent GCT cases (73.6%) was statistically higher than that for non-recurrent cases (29.1%). CONCLUSION: In the diagnosis of GCT, p63 is a useful but not a conclusive marker. However, p63 did appear to indicate the biological aggressiveness of GCT. Therefore, p63 may help surgeons to estimate the risk of recurrence after surgery and help them to choose the best treatment for each GCT case. Informa Healthcare 2013-03 2013-02-13 /pmc/articles/PMC3572666/ /pubmed/23033898 http://dx.doi.org/10.3109/03009734.2012.724731 Text en © Informa Healthcare http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the source is credited.
spellingShingle Original Article
Yanagisawa, Michiro
kakizaki, Hiroshi
Okada, Kyoji
Torigoe, Tomoaki
Kusumi, Tomomi
p63 as a prognostic marker for giant cell tumor of bone
title p63 as a prognostic marker for giant cell tumor of bone
title_full p63 as a prognostic marker for giant cell tumor of bone
title_fullStr p63 as a prognostic marker for giant cell tumor of bone
title_full_unstemmed p63 as a prognostic marker for giant cell tumor of bone
title_short p63 as a prognostic marker for giant cell tumor of bone
title_sort p63 as a prognostic marker for giant cell tumor of bone
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3572666/
https://www.ncbi.nlm.nih.gov/pubmed/23033898
http://dx.doi.org/10.3109/03009734.2012.724731
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