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Ossifying Fibromyxoid Tumour

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Abstract

Myxoid soft tissue neoplasms of the face and orbit may present in non-specific patterns with symptoms depending on affected structures. These are mesenchymal neoplasms characterized by the production of abundant extracellular myxoid matrix that can be categorized as benign or malignant. Among them, ossifying fibromyxoid tumour is a rare form with borderline malignant potential. Around 70% is said to arise from extremities and would occasionally involve the trunk, head and neck, oral cavity, mediastinum, and retroperitoneum. It has been reported in only 150 cases in literature, rarely in the orbit, with the first case being reported in 2006.

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Further Reading

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Correspondence to Shantha Amrith .

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Parulan, M.A. et al. (2019). Ossifying Fibromyxoid Tumour. In: Amrith, S., Sundar, G., Young, S. (eds) Ocular Adnexal Lesions. Springer, Singapore. https://doi.org/10.1007/978-981-13-3798-7_30

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  • DOI: https://doi.org/10.1007/978-981-13-3798-7_30

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  • Publisher Name: Springer, Singapore

  • Print ISBN: 978-981-13-3797-0

  • Online ISBN: 978-981-13-3798-7

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