| Literature DB >> 25336010 |
Kunihiko Moriya1, Saori Katayama, Masaei Onuma, Takeshi Rikiishi, Masami Hosaka, Mika Watanabe, Tadashi Hasegawa, Yoji Sasahara, Shigeo Kure.
Abstract
Mesenchymal chondrosarcoma (MC) is an extremely rare subtype of chondrosarcoma that has a small round-cell sarcoma with focal cartilaginous differentiation, often with a pericytomatous vascular pattern. The non-cartilaginous components are usually dominant, and such lesions might be confused with other small round-cell tumors. Recently, a tumor-specific HEY1-NCOA2 fusion gene was identified in MC. Here we report the case of a 9-year-old boy who was diagnosed with MC by detection of HEY1-NCOA2 fusion signals in almost 50% of tumor cells in tissue sections on fluorescence in situ hybridization (FISH). In this way, the tumor was definitively diagnosed as MC. This case suggests that the detection of the HEY1-NCOA2 fusion gene on FISH is of diagnostic value for MC.Entities:
Keywords: HEY1-NCOA2 fusion gene; fluorescence in situ hybridization; mesenchymal chondrosarcoma
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Year: 2014 PMID: 25336010 DOI: 10.1111/ped.12407
Source DB: PubMed Journal: Pediatr Int ISSN: 1328-8067 Impact factor: 1.524