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BCOR-CCNB3 sarcoma arising in the proximal tibia: A case report

BCL6 corepressor-cyclin B3 (BCOR-CCNB3) fusion sarcoma was classified as an emerging subgroup of undifferentiated small round cell sarcoma in 2020. The incidence of BCOR-CCNB3 fusion sarcoma is reportedly 1.5-14% among undifferentiated unclassified sarcomas, representing a rare entity among primary...

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Autores principales: Suzuki, Kayo, Yasuda, Taketoshi, Haruhara, Yuki, Watanabe, Kenta, Nomura, Keiko, Kanamori, Masahiko, Kawaguchi, Yoshiharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892468/
https://www.ncbi.nlm.nih.gov/pubmed/35251628
http://dx.doi.org/10.3892/mco.2022.2510
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author Suzuki, Kayo
Yasuda, Taketoshi
Haruhara, Yuki
Watanabe, Kenta
Nomura, Keiko
Kanamori, Masahiko
Kawaguchi, Yoshiharu
author_facet Suzuki, Kayo
Yasuda, Taketoshi
Haruhara, Yuki
Watanabe, Kenta
Nomura, Keiko
Kanamori, Masahiko
Kawaguchi, Yoshiharu
author_sort Suzuki, Kayo
collection PubMed
description BCL6 corepressor-cyclin B3 (BCOR-CCNB3) fusion sarcoma was classified as an emerging subgroup of undifferentiated small round cell sarcoma in 2020. The incidence of BCOR-CCNB3 fusion sarcoma is reportedly 1.5-14% among undifferentiated unclassified sarcomas, representing a rare entity among primary malignant bone tumors. The present study reports a case of BCOR-CCNB3 fusion sarcoma in the proximal tibia of a boy. A 12-year-old boy presented with a 6-month history of knee pain and a slowly growing mass in the anteromedial aspect of the left proximal tibia. Plain radiography and computed tomography of the knee demonstrated a lytic lesion with cortical destruction of the proximal tibia. Magnetic resonance imaging showed the bone tumor expanding into soft tissue with almost homogeneous hypointensity on T1-weighted imaging and slightly hyperintensity on T2-weighted imaging. On histopathological evaluation, the tumor comprised a proliferation of small, round to ovoid-shaped mesenchymal cells without osteoid formation. Histopathologically, BCOR-CCNB3 sarcoma of bone was finally diagnosed based on immunohistochemical staining and additional molecular analyses. The patient underwent bone tumor resection followed by pre- and post-operative chemotherapy according to a Ewing sarcoma protocol. The patient showed no evidence of local recurrence or distant metastasis at 12 months after completion of adjuvant chemotherapy. We present herein an additional case of BCOR-CCNB3 sarcoma of the proximal tibia, and review the relevant literature on BCOR-CCNB3 sarcoma of bone.
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spelling pubmed-88924682022-03-04 BCOR-CCNB3 sarcoma arising in the proximal tibia: A case report Suzuki, Kayo Yasuda, Taketoshi Haruhara, Yuki Watanabe, Kenta Nomura, Keiko Kanamori, Masahiko Kawaguchi, Yoshiharu Mol Clin Oncol Case Report BCL6 corepressor-cyclin B3 (BCOR-CCNB3) fusion sarcoma was classified as an emerging subgroup of undifferentiated small round cell sarcoma in 2020. The incidence of BCOR-CCNB3 fusion sarcoma is reportedly 1.5-14% among undifferentiated unclassified sarcomas, representing a rare entity among primary malignant bone tumors. The present study reports a case of BCOR-CCNB3 fusion sarcoma in the proximal tibia of a boy. A 12-year-old boy presented with a 6-month history of knee pain and a slowly growing mass in the anteromedial aspect of the left proximal tibia. Plain radiography and computed tomography of the knee demonstrated a lytic lesion with cortical destruction of the proximal tibia. Magnetic resonance imaging showed the bone tumor expanding into soft tissue with almost homogeneous hypointensity on T1-weighted imaging and slightly hyperintensity on T2-weighted imaging. On histopathological evaluation, the tumor comprised a proliferation of small, round to ovoid-shaped mesenchymal cells without osteoid formation. Histopathologically, BCOR-CCNB3 sarcoma of bone was finally diagnosed based on immunohistochemical staining and additional molecular analyses. The patient underwent bone tumor resection followed by pre- and post-operative chemotherapy according to a Ewing sarcoma protocol. The patient showed no evidence of local recurrence or distant metastasis at 12 months after completion of adjuvant chemotherapy. We present herein an additional case of BCOR-CCNB3 sarcoma of the proximal tibia, and review the relevant literature on BCOR-CCNB3 sarcoma of bone. D.A. Spandidos 2022-04 2022-02-07 /pmc/articles/PMC8892468/ /pubmed/35251628 http://dx.doi.org/10.3892/mco.2022.2510 Text en Copyright: © Suzuki et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Case Report
Suzuki, Kayo
Yasuda, Taketoshi
Haruhara, Yuki
Watanabe, Kenta
Nomura, Keiko
Kanamori, Masahiko
Kawaguchi, Yoshiharu
BCOR-CCNB3 sarcoma arising in the proximal tibia: A case report
title BCOR-CCNB3 sarcoma arising in the proximal tibia: A case report
title_full BCOR-CCNB3 sarcoma arising in the proximal tibia: A case report
title_fullStr BCOR-CCNB3 sarcoma arising in the proximal tibia: A case report
title_full_unstemmed BCOR-CCNB3 sarcoma arising in the proximal tibia: A case report
title_short BCOR-CCNB3 sarcoma arising in the proximal tibia: A case report
title_sort bcor-ccnb3 sarcoma arising in the proximal tibia: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892468/
https://www.ncbi.nlm.nih.gov/pubmed/35251628
http://dx.doi.org/10.3892/mco.2022.2510
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