Volume 56, Issue 5 pp. e55-e57
Patient Report

Mesenchymal chondrosarcoma diagnosed on FISH for HEY1-NCOA2 fusion gene

Kunihiko Moriya

Corresponding Author

Kunihiko Moriya

Department of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Miyagi

Correspondence: Kunihiko Moriya, MD, PhD, Department of Pediatrics, Tohoku University Graduate School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8574, Japan. Email: [email protected]Search for more papers by this author
Saori Katayama

Saori Katayama

Department of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Miyagi

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Masaei Onuma

Masaei Onuma

Department of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Miyagi

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Takeshi Rikiishi

Takeshi Rikiishi

Department of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Miyagi

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Masami Hosaka

Masami Hosaka

Department of Orthopedic Surgery, Tohoku University Graduate School of Medicine, Sendai, Miyagi

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Mika Watanabe

Mika Watanabe

Department of Pathology, Tohoku University Hospital, Sendai, Miyagi

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Tadashi Hasegawa

Tadashi Hasegawa

Department of Surgical Pathology, Sapporo Medical University School of Medicine, Sapporo, Hokkaido, Japan

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Yoji Sasahara

Yoji Sasahara

Department of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Miyagi

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Shigeo Kure

Shigeo Kure

Department of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Miyagi

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First published: 22 October 2014
Citations: 15

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.

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