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CD10-positive mantle cell lymphoma: clinicopathologic and prognostic study of 30 cases

Mantle cell lymphoma is usually negative for CD10 which is useful in distinguishing MCL from other CD10 + B cell lymphomas. Here we assessed the clinicopathologic features of 30 cases of CD10+ MCL, the largest series to date in the English literature, and compared them with a group of 212 typical MC...

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Autores principales: Xu, Jie, Medeiros, L. Jeffrey, Saksena, Annapurna, Wang, Michael, Zhou, Jiehao, Li, Jingyi, Yin, C. Cameron, Tang, Guilin, Wang, Lifu, Lin, Pei, Li, Shaoying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5837746/
https://www.ncbi.nlm.nih.gov/pubmed/29545910
http://dx.doi.org/10.18632/oncotarget.23571
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author Xu, Jie
Medeiros, L. Jeffrey
Saksena, Annapurna
Wang, Michael
Zhou, Jiehao
Li, Jingyi
Yin, C. Cameron
Tang, Guilin
Wang, Lifu
Lin, Pei
Li, Shaoying
author_facet Xu, Jie
Medeiros, L. Jeffrey
Saksena, Annapurna
Wang, Michael
Zhou, Jiehao
Li, Jingyi
Yin, C. Cameron
Tang, Guilin
Wang, Lifu
Lin, Pei
Li, Shaoying
author_sort Xu, Jie
collection PubMed
description Mantle cell lymphoma is usually negative for CD10 which is useful in distinguishing MCL from other CD10 + B cell lymphomas. Here we assessed the clinicopathologic features of 30 cases of CD10+ MCL, the largest series to date in the English literature, and compared them with a group of 212 typical MCL cases (CD5+, CD10-negative, CD23-negative, cyclin D1+). The 30 patients with CD10+ MCL included 17 men and 13 women with a median age of 68 years. Compared with CD10-negative MCL, patients with CD10+ MCL showed a lower male predominance (p = 0.01), more often had a diffuse growth pattern (p = 0.04) and blastoid/pleomorphic morphology (p < 0.0001), and more often showed BCL6 expression (p = 0.009). In all MCL patients, CD10 expression was not associated with overall survival (OS) (p = 0.16). However, in more aggressive subsets of MCL patients including those with high Ki67 (> 60%), blastoid/pleomorphic morphology, or high MCL International Prognostic Index (MIPI), CD10 expression was associated with a worse OS (p = 0.003, 0.04, and 0.001, respectively). High Ki67 (> 60%), blastoid/pleomorphic morphology, and high MIPI were also been identified as poor prognostic factors patients with in CD10+ MCL (p = 0.001, 0.0003, and 0.01, respectively). In summary, CD10+ MCL more often has a diffuse growth pattern, blastoid/pleomorphic morphology, and BCL6 expression. In MCL patients with a high Ki-67 (> 60%), blastoid/pleomorphic morphology, or high MIPI, CD10 expression contributes to an even worse prognosis. MCL should be included in the differential diagnosis of CD10 + B cell lymphomas.
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spelling pubmed-58377462018-03-15 CD10-positive mantle cell lymphoma: clinicopathologic and prognostic study of 30 cases Xu, Jie Medeiros, L. Jeffrey Saksena, Annapurna Wang, Michael Zhou, Jiehao Li, Jingyi Yin, C. Cameron Tang, Guilin Wang, Lifu Lin, Pei Li, Shaoying Oncotarget Research Paper: Pathology Mantle cell lymphoma is usually negative for CD10 which is useful in distinguishing MCL from other CD10 + B cell lymphomas. Here we assessed the clinicopathologic features of 30 cases of CD10+ MCL, the largest series to date in the English literature, and compared them with a group of 212 typical MCL cases (CD5+, CD10-negative, CD23-negative, cyclin D1+). The 30 patients with CD10+ MCL included 17 men and 13 women with a median age of 68 years. Compared with CD10-negative MCL, patients with CD10+ MCL showed a lower male predominance (p = 0.01), more often had a diffuse growth pattern (p = 0.04) and blastoid/pleomorphic morphology (p < 0.0001), and more often showed BCL6 expression (p = 0.009). In all MCL patients, CD10 expression was not associated with overall survival (OS) (p = 0.16). However, in more aggressive subsets of MCL patients including those with high Ki67 (> 60%), blastoid/pleomorphic morphology, or high MCL International Prognostic Index (MIPI), CD10 expression was associated with a worse OS (p = 0.003, 0.04, and 0.001, respectively). High Ki67 (> 60%), blastoid/pleomorphic morphology, and high MIPI were also been identified as poor prognostic factors patients with in CD10+ MCL (p = 0.001, 0.0003, and 0.01, respectively). In summary, CD10+ MCL more often has a diffuse growth pattern, blastoid/pleomorphic morphology, and BCL6 expression. In MCL patients with a high Ki-67 (> 60%), blastoid/pleomorphic morphology, or high MIPI, CD10 expression contributes to an even worse prognosis. MCL should be included in the differential diagnosis of CD10 + B cell lymphomas. Impact Journals LLC 2017-12-15 /pmc/articles/PMC5837746/ /pubmed/29545910 http://dx.doi.org/10.18632/oncotarget.23571 Text en Copyright: © 2018 Xu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper: Pathology
Xu, Jie
Medeiros, L. Jeffrey
Saksena, Annapurna
Wang, Michael
Zhou, Jiehao
Li, Jingyi
Yin, C. Cameron
Tang, Guilin
Wang, Lifu
Lin, Pei
Li, Shaoying
CD10-positive mantle cell lymphoma: clinicopathologic and prognostic study of 30 cases
title CD10-positive mantle cell lymphoma: clinicopathologic and prognostic study of 30 cases
title_full CD10-positive mantle cell lymphoma: clinicopathologic and prognostic study of 30 cases
title_fullStr CD10-positive mantle cell lymphoma: clinicopathologic and prognostic study of 30 cases
title_full_unstemmed CD10-positive mantle cell lymphoma: clinicopathologic and prognostic study of 30 cases
title_short CD10-positive mantle cell lymphoma: clinicopathologic and prognostic study of 30 cases
title_sort cd10-positive mantle cell lymphoma: clinicopathologic and prognostic study of 30 cases
topic Research Paper: Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5837746/
https://www.ncbi.nlm.nih.gov/pubmed/29545910
http://dx.doi.org/10.18632/oncotarget.23571
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