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Plasmacytoma in patients with multiple myeloma: morphology and immunohistochemistry

BACKGROUND: To study the histological structure and immunohistochemical (IHC) parameters of the plasmacytoma tumour substrate in patients with multiple myeloma (MM). METHODS: The study included 21 patients (10 men/11 women) aged 23 to 73 years old with newly diagnosed MM complicated by plasmacytoma....

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Autores principales: Firsova, Maiia V., Mendeleeva, Larisa P., Kovrigina, Alla M., Solovev, Maxim V., Savchenko, Valery G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178964/
https://www.ncbi.nlm.nih.gov/pubmed/32321465
http://dx.doi.org/10.1186/s12885-020-06870-w
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author Firsova, Maiia V.
Mendeleeva, Larisa P.
Kovrigina, Alla M.
Solovev, Maxim V.
Savchenko, Valery G.
author_facet Firsova, Maiia V.
Mendeleeva, Larisa P.
Kovrigina, Alla M.
Solovev, Maxim V.
Savchenko, Valery G.
author_sort Firsova, Maiia V.
collection PubMed
description BACKGROUND: To study the histological structure and immunohistochemical (IHC) parameters of the plasmacytoma tumour substrate in patients with multiple myeloma (MM). METHODS: The study included 21 patients (10 men/11 women) aged 23 to 73 years old with newly diagnosed MM complicated by plasmacytoma. Bone plasmacytoma was diagnosed in 14 patients, and extramedullary plasmacytoma was diagnosed in 7 patients. Plasmacytoma tissue specimens were examined using a LEICA DM4000B microscope. Anti-CD56, anti-CD166, anti-CXCR4, anti-Ki-67, and anti-c-MYC antibodies were used for IHC study of plasmacytoma biopsies. RESULTS: When comparing the morphology of bone and extramedullary plasmacytoma, no significant differences were revealed; however, the substrate of extramedullary plasmacytoma was more often represented by tumour cells with an immature morphology than was the bone plasmacytoma substrate (57.1% vs. 28.6%, respectively). We revealed a significant difference in the expression of CD166 between bone and extramedullary plasmacytoma. The mean values ​​of CD166 expression in bone plasmacytoma cells were significantly higher (36.29 ± 7.61% versus 9.57 ± 8.46%, respectively; p = 0.033) than those in extramedullary plasmacytoma cells. We noticed that in extramedullary plasmacytoma cells, there were higher values for the Ki-67 index than in bone plasmacytoma cells, and this result was independent of cell morphology. CONCLUSION: The mechanisms involved in the dissemination of tumour plasma cells are currently unexplored. Even in such a small sample, some differences in expression could be identified, which may indicate that different mechanisms lead to the formation of bone and extramedullary plasmacytomas. Specifically, the expression of CD166 in extramedullary plasmacytoma cells was almost 4 times lower than that in bone plasmacytoma cells, which may indicate the involvement of CD166 in the mechanisms of bone destruction. The proliferative activity of extramedullary plasmacytoma cells was shown to be higher than that of bone plasmacytoma cells.
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spelling pubmed-71789642020-04-26 Plasmacytoma in patients with multiple myeloma: morphology and immunohistochemistry Firsova, Maiia V. Mendeleeva, Larisa P. Kovrigina, Alla M. Solovev, Maxim V. Savchenko, Valery G. BMC Cancer Research Article BACKGROUND: To study the histological structure and immunohistochemical (IHC) parameters of the plasmacytoma tumour substrate in patients with multiple myeloma (MM). METHODS: The study included 21 patients (10 men/11 women) aged 23 to 73 years old with newly diagnosed MM complicated by plasmacytoma. Bone plasmacytoma was diagnosed in 14 patients, and extramedullary plasmacytoma was diagnosed in 7 patients. Plasmacytoma tissue specimens were examined using a LEICA DM4000B microscope. Anti-CD56, anti-CD166, anti-CXCR4, anti-Ki-67, and anti-c-MYC antibodies were used for IHC study of plasmacytoma biopsies. RESULTS: When comparing the morphology of bone and extramedullary plasmacytoma, no significant differences were revealed; however, the substrate of extramedullary plasmacytoma was more often represented by tumour cells with an immature morphology than was the bone plasmacytoma substrate (57.1% vs. 28.6%, respectively). We revealed a significant difference in the expression of CD166 between bone and extramedullary plasmacytoma. The mean values ​​of CD166 expression in bone plasmacytoma cells were significantly higher (36.29 ± 7.61% versus 9.57 ± 8.46%, respectively; p = 0.033) than those in extramedullary plasmacytoma cells. We noticed that in extramedullary plasmacytoma cells, there were higher values for the Ki-67 index than in bone plasmacytoma cells, and this result was independent of cell morphology. CONCLUSION: The mechanisms involved in the dissemination of tumour plasma cells are currently unexplored. Even in such a small sample, some differences in expression could be identified, which may indicate that different mechanisms lead to the formation of bone and extramedullary plasmacytomas. Specifically, the expression of CD166 in extramedullary plasmacytoma cells was almost 4 times lower than that in bone plasmacytoma cells, which may indicate the involvement of CD166 in the mechanisms of bone destruction. The proliferative activity of extramedullary plasmacytoma cells was shown to be higher than that of bone plasmacytoma cells. BioMed Central 2020-04-22 /pmc/articles/PMC7178964/ /pubmed/32321465 http://dx.doi.org/10.1186/s12885-020-06870-w Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Firsova, Maiia V.
Mendeleeva, Larisa P.
Kovrigina, Alla M.
Solovev, Maxim V.
Savchenko, Valery G.
Plasmacytoma in patients with multiple myeloma: morphology and immunohistochemistry
title Plasmacytoma in patients with multiple myeloma: morphology and immunohistochemistry
title_full Plasmacytoma in patients with multiple myeloma: morphology and immunohistochemistry
title_fullStr Plasmacytoma in patients with multiple myeloma: morphology and immunohistochemistry
title_full_unstemmed Plasmacytoma in patients with multiple myeloma: morphology and immunohistochemistry
title_short Plasmacytoma in patients with multiple myeloma: morphology and immunohistochemistry
title_sort plasmacytoma in patients with multiple myeloma: morphology and immunohistochemistry
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178964/
https://www.ncbi.nlm.nih.gov/pubmed/32321465
http://dx.doi.org/10.1186/s12885-020-06870-w
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