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Sporadic Burkitt lymphomas of children and adolescents in Chinese: a clinicopathological study of 43 cases

BACKGROUND: To investigate the clinical and pathologic features as well as the MYC translocations of childhood Burkitt lymphoma (BL) from China. METHODS: Fourty-three cases of childhood BL were retrospectively investigated in morphology, immunophenotype, genotype, treatments and survival analysis. R...

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Autores principales: Bi, Cheng-Feng, Tang, Yuan, Zhang, Wen-Yan, Zhao, Sha, Wang, Xiao-Qing, Yang, Qun-Pei, Li, Gan-Di, Liu, Wei-ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414834/
https://www.ncbi.nlm.nih.gov/pubmed/22726497
http://dx.doi.org/10.1186/1746-1596-7-72
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author Bi, Cheng-Feng
Tang, Yuan
Zhang, Wen-Yan
Zhao, Sha
Wang, Xiao-Qing
Yang, Qun-Pei
Li, Gan-Di
Liu, Wei-ping
author_facet Bi, Cheng-Feng
Tang, Yuan
Zhang, Wen-Yan
Zhao, Sha
Wang, Xiao-Qing
Yang, Qun-Pei
Li, Gan-Di
Liu, Wei-ping
author_sort Bi, Cheng-Feng
collection PubMed
description BACKGROUND: To investigate the clinical and pathologic features as well as the MYC translocations of childhood Burkitt lymphoma (BL) from China. METHODS: Fourty-three cases of childhood BL were retrospectively investigated in morphology, immunophenotype, genotype, treatments and survival analysis. RESULTS: Clinically, there was a marked male predominance in sex distribution (M: F = 9.75:1); abdomen was the most frequent extranodal sites of involvement (46.5 %), followed by jaws and facial bones (16.3 %). Two third of the patients were in stageI ~ II. Morphologically, 69.76 % of the cases showed classical histologic features, while 30.24 % of them showed greater nuclear pleomorphism in size and shape. Five cases (11.6 %) were positive for EBER1/2. Thirty-one of the 40 cases (77.5 %) had the aberration of IGH/MYC translocation while 7 (17.5 %) had non-IGH/MYC translocation. Thirty patients (69.7 %) received operation and/or chemotherapy while 13 patients (30.3 %) received no treatment. Twenty-seven patients (62.8 %) died of the tumor, 16 alive, with the average survival time 4.9 and 48.7 months respectively. High IPI, advanced clinical stage, increased serum level of LDH and no chemotherapy received as well as tumor size ≥10 cm were related to the lower survival rates of the tumor. CONCLUSIONS: Several differences were showed in this group of BL, including a much higher ratio of male patients, more cases in stageII, clinically inconsistent treatment and a very poor outcome. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here http://www.diagnosticpathology.diagnomx.eu/vs/1552295877710135
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spelling pubmed-34148342012-08-10 Sporadic Burkitt lymphomas of children and adolescents in Chinese: a clinicopathological study of 43 cases Bi, Cheng-Feng Tang, Yuan Zhang, Wen-Yan Zhao, Sha Wang, Xiao-Qing Yang, Qun-Pei Li, Gan-Di Liu, Wei-ping Diagn Pathol Research BACKGROUND: To investigate the clinical and pathologic features as well as the MYC translocations of childhood Burkitt lymphoma (BL) from China. METHODS: Fourty-three cases of childhood BL were retrospectively investigated in morphology, immunophenotype, genotype, treatments and survival analysis. RESULTS: Clinically, there was a marked male predominance in sex distribution (M: F = 9.75:1); abdomen was the most frequent extranodal sites of involvement (46.5 %), followed by jaws and facial bones (16.3 %). Two third of the patients were in stageI ~ II. Morphologically, 69.76 % of the cases showed classical histologic features, while 30.24 % of them showed greater nuclear pleomorphism in size and shape. Five cases (11.6 %) were positive for EBER1/2. Thirty-one of the 40 cases (77.5 %) had the aberration of IGH/MYC translocation while 7 (17.5 %) had non-IGH/MYC translocation. Thirty patients (69.7 %) received operation and/or chemotherapy while 13 patients (30.3 %) received no treatment. Twenty-seven patients (62.8 %) died of the tumor, 16 alive, with the average survival time 4.9 and 48.7 months respectively. High IPI, advanced clinical stage, increased serum level of LDH and no chemotherapy received as well as tumor size ≥10 cm were related to the lower survival rates of the tumor. CONCLUSIONS: Several differences were showed in this group of BL, including a much higher ratio of male patients, more cases in stageII, clinically inconsistent treatment and a very poor outcome. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here http://www.diagnosticpathology.diagnomx.eu/vs/1552295877710135 BioMed Central 2012-06-22 /pmc/articles/PMC3414834/ /pubmed/22726497 http://dx.doi.org/10.1186/1746-1596-7-72 Text en Copyright ©2012 Bi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Bi, Cheng-Feng
Tang, Yuan
Zhang, Wen-Yan
Zhao, Sha
Wang, Xiao-Qing
Yang, Qun-Pei
Li, Gan-Di
Liu, Wei-ping
Sporadic Burkitt lymphomas of children and adolescents in Chinese: a clinicopathological study of 43 cases
title Sporadic Burkitt lymphomas of children and adolescents in Chinese: a clinicopathological study of 43 cases
title_full Sporadic Burkitt lymphomas of children and adolescents in Chinese: a clinicopathological study of 43 cases
title_fullStr Sporadic Burkitt lymphomas of children and adolescents in Chinese: a clinicopathological study of 43 cases
title_full_unstemmed Sporadic Burkitt lymphomas of children and adolescents in Chinese: a clinicopathological study of 43 cases
title_short Sporadic Burkitt lymphomas of children and adolescents in Chinese: a clinicopathological study of 43 cases
title_sort sporadic burkitt lymphomas of children and adolescents in chinese: a clinicopathological study of 43 cases
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414834/
https://www.ncbi.nlm.nih.gov/pubmed/22726497
http://dx.doi.org/10.1186/1746-1596-7-72
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