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Reports on BCOR-CCNB3 sarcoma in the head and neck region are scarce, given their unknown etiology. An 18-year-old male patient presented a rapidly enlarging tumor extending from the right nasopharynx to the oropharynx. Histological examination showed a spindle cell sarcoma with BCOR-CCNB3 fusion detected by fluorescence in situ hybridization, and BCOR-CCNB3 was diagnosed. After three courses of alternating VDC-IE therapy, the patient underwent tumor resection based on the original tumor range with a minimal margin, using the mandibular swing technique. Radiation therapy (50.4 Gy) was administered postoperatively, followed by three additional courses of alternating VDC-IE therapy. The patient survived and showed no evidence of disease at 12 months postoperatively. BCOR-CCNB3 sarcoma is a chemotherapy-sensitive sarcoma, and conservative resection with a minimal margin that does not interfere with the treatment flow is preferable.
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http://dx.doi.org/10.1016/j.anl.2022.04.012 | DOI Listing |
Surg Pathol Clin
September 2025
Department of Diagnostic Pathology, National Cancer Center Hospital, 5-1-1, Tsukiji, Chuo-ku, Tokyo 104-0045, Japan; Rare Cancer Center, National Cancer Center Hospital, Tokyo, Japan. Electronic address:
Undifferentiated small round cell sarcomas are a heterogeneous group of high-grade sarcomas of uncertain histogenesis. In this review, the key clinicopathological, immunohistochemical, and molecular characteristics of select entities that commonly originate from bones (ie, Ewing sarcoma, BCOR::CCNB3 sarcoma, and EWSR1::NFATC2 sarcomas) are summarized. CIC-rearranged sarcomas are briefly discussed because they rarely arise from bone.
View Article and Find Full Text PDFJpn J Clin Oncol
July 2025
Department of Orthopaedic Surgery, Teikyo University School of Medicine, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan.
BCOR::CCNB3 sarcoma is a rare sarcoma defined by the BCOR::CCNB3 fusion gene. It predominantly affects males under 20, with a slight predominance of bone origin. Initially grouped as 'Ewing-like,' it is now a distinct entity, a major part of 'sarcoma with BCOR genetic alterations.
View Article and Find Full Text PDFCytopathology
June 2025
Pathology Department, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
BCOR-CCNB3 sarcoma is an undifferentiated small round cell sarcoma characterised by distinct molecular genetic alterations. The diagnostic clues include tumour cells with oval to short spindle-shaped morphology, finely dispersed chromatin, inconspicuous nucleoli, and an arrangement around blood vessels that forms pseudopapillary structures.
View Article and Find Full Text PDFFetal Pediatr Pathol
July 2025
Pediatric Oncology, All India Institute of Medical Sciences, New Delhi, India.
BCOR-altered sarcomas (BAS) are a subset of undifferentiated small round cell sarcomas characterized by alterations involving the BCOR gene. These tumors often pose diagnostic challenges due to their morphological overlap with other pediatric neoplasms. We report a case of BAS in an infant presenting with bilateral lower limb weakness.
View Article and Find Full Text PDFAm J Surg Pathol
April 2025
Department of Pathology, Istanbul University, Istanbul Faculty of Medicine.
In this study, we aimed to reclassify "round cell sarcomas" identified in the Department of Pathology, Istanbul Faculty of Medicine, Istanbul University, between 2013 and 2023, using an immunohistochemical panel including CD99, NKX2.2, ETV4, WT1, DUX4, BCOR, CCNB3, and SS18-SSX antibodies, fluorescence in situ hybridization (FISH), and next-generation sequencing (NGS). A total of 148 Ewing's sarcomas, 21 CIC::DUX4 sarcomas, and 18 BCOR::CCNB3 sarcomas were diagnosed.
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