Case Report: BRCA1 and BRCA2 loss in a young man with primary cutaneous extraskeletal osteosarcoma

BackgroundExtraskeletal osteosarcoma is an uncommon and high-grade soft tissue malignancy. The incidence is even lower when the skin is the primary site. To the best of our knowledge, the primary cutaneous osteosarcoma has fewer than 30 reported cases worldwide, which with decreased copy number ofBR...

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Main Authors: Wen-Feng Luo, Yu-Hang Hou, Yu-Teng Huang, Jun-Dong Lai, Hui-Shan Jiang, Wei-Liang Wang
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-03-01
Series:Frontiers in Oncology
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Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2025.1504366/full
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author Wen-Feng Luo
Yu-Hang Hou
Yu-Teng Huang
Jun-Dong Lai
Hui-Shan Jiang
Wei-Liang Wang
author_facet Wen-Feng Luo
Yu-Hang Hou
Yu-Teng Huang
Jun-Dong Lai
Hui-Shan Jiang
Wei-Liang Wang
author_sort Wen-Feng Luo
collection DOAJ
description BackgroundExtraskeletal osteosarcoma is an uncommon and high-grade soft tissue malignancy. The incidence is even lower when the skin is the primary site. To the best of our knowledge, the primary cutaneous osteosarcoma has fewer than 30 reported cases worldwide, which with decreased copy number ofBRCA1 and BRCA2 has never been reported before.Case presentationA 28-year-old man was hospitalized for a skin mass on the left shoulder. The histological examination showed a large number of tumor giant cells and fibroblasts, and nuclear division was easy to see. Immunohistochemistry showed positive for CK, EMA, S100, CD34, CK7, Bcl-2, ACTin, and NSE, and negative for Vim, SATB2, CD99, SMA (focal), and Ki67 was about 40%. Shoulder joint CT and PET-CT showed that no metastasis presented. Germline testing showed decreased copy number ofBRCA1 and BRCA2. The diagnosis was cutaneous extraskeletal osteosarcomas of the left shoulder. The patient underwent an enlarged resection, followed by local radiotherapy four cycles. No recurrence or metastasis occurred on a 1-year of follow-up.ConclusionsPrimary cutaneous extraskeletal osteosarcoma (PC-EOS) is rare, and preoperative differential diagnosis is difficult. This is the first report of PC-EOS with decreased copy number of BRCA1 and BRCA2. The presented case highlights the importance of accurate histopathological examination and comprehensive analysis. We considered that BRCA1 and BRCA2 genes may are associated with a worse outcome and local recurrence in PC-EOS. But, it may not have been fully recognized.
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spelling doaj-art-5df7cab473224d47bc91d144a1de3e442025-08-20T02:02:13ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2025-03-011510.3389/fonc.2025.15043661504366Case Report: BRCA1 and BRCA2 loss in a young man with primary cutaneous extraskeletal osteosarcomaWen-Feng Luo0Yu-Hang Hou1Yu-Teng Huang2Jun-Dong Lai3Hui-Shan Jiang4Wei-Liang Wang5Guangdong Medical University, Zhanjiang, Guangdong, ChinaGuangdong Medical University, Zhanjiang, Guangdong, ChinaGuangdong Medical University, Zhanjiang, Guangdong, ChinaYangjiang People’s Hospital affiliated to Guangdong Medical University, Yangjiang, Guangdong, ChinaYangjiang People’s Hospital affiliated to Guangdong Medical University, Yangjiang, Guangdong, ChinaYangjiang People’s Hospital affiliated to Guangdong Medical University, Yangjiang, Guangdong, ChinaBackgroundExtraskeletal osteosarcoma is an uncommon and high-grade soft tissue malignancy. The incidence is even lower when the skin is the primary site. To the best of our knowledge, the primary cutaneous osteosarcoma has fewer than 30 reported cases worldwide, which with decreased copy number ofBRCA1 and BRCA2 has never been reported before.Case presentationA 28-year-old man was hospitalized for a skin mass on the left shoulder. The histological examination showed a large number of tumor giant cells and fibroblasts, and nuclear division was easy to see. Immunohistochemistry showed positive for CK, EMA, S100, CD34, CK7, Bcl-2, ACTin, and NSE, and negative for Vim, SATB2, CD99, SMA (focal), and Ki67 was about 40%. Shoulder joint CT and PET-CT showed that no metastasis presented. Germline testing showed decreased copy number ofBRCA1 and BRCA2. The diagnosis was cutaneous extraskeletal osteosarcomas of the left shoulder. The patient underwent an enlarged resection, followed by local radiotherapy four cycles. No recurrence or metastasis occurred on a 1-year of follow-up.ConclusionsPrimary cutaneous extraskeletal osteosarcoma (PC-EOS) is rare, and preoperative differential diagnosis is difficult. This is the first report of PC-EOS with decreased copy number of BRCA1 and BRCA2. The presented case highlights the importance of accurate histopathological examination and comprehensive analysis. We considered that BRCA1 and BRCA2 genes may are associated with a worse outcome and local recurrence in PC-EOS. But, it may not have been fully recognized.https://www.frontiersin.org/articles/10.3389/fonc.2025.1504366/fullosteosarcomaprimary cutaneous extraskeletal osteosarcomasoft tissue tumorBRCA1BRCA2
spellingShingle Wen-Feng Luo
Yu-Hang Hou
Yu-Teng Huang
Jun-Dong Lai
Hui-Shan Jiang
Wei-Liang Wang
Case Report: BRCA1 and BRCA2 loss in a young man with primary cutaneous extraskeletal osteosarcoma
Frontiers in Oncology
osteosarcoma
primary cutaneous extraskeletal osteosarcoma
soft tissue tumor
BRCA1
BRCA2
title Case Report: BRCA1 and BRCA2 loss in a young man with primary cutaneous extraskeletal osteosarcoma
title_full Case Report: BRCA1 and BRCA2 loss in a young man with primary cutaneous extraskeletal osteosarcoma
title_fullStr Case Report: BRCA1 and BRCA2 loss in a young man with primary cutaneous extraskeletal osteosarcoma
title_full_unstemmed Case Report: BRCA1 and BRCA2 loss in a young man with primary cutaneous extraskeletal osteosarcoma
title_short Case Report: BRCA1 and BRCA2 loss in a young man with primary cutaneous extraskeletal osteosarcoma
title_sort case report brca1 and brca2 loss in a young man with primary cutaneous extraskeletal osteosarcoma
topic osteosarcoma
primary cutaneous extraskeletal osteosarcoma
soft tissue tumor
BRCA1
BRCA2
url https://www.frontiersin.org/articles/10.3389/fonc.2025.1504366/full
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