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Zampieri N et al. – Desmoid tumour is relatively rare and generally non–metastatisizing lesion of mesenchymal origin composed of fibrous tissue and fitting in the group of aggressive fibromatosis; it is a locally aggressive proliferative soft–tissue lesion with controversial nature. This is a rare case of extra–abdominal desmoid tumour in a 14–year–old girl affected by spastic tetraparesis.

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