Cordoma sacrococcígeo: revisión del tema

Author:

Sánchez Torres Luis Jair,Pulido Torres Héctor Alejandro,Espinoza Velazco Absalón,Pérez Pineda Perla Lidia,Chávez Reyna María Magdalena

Publisher

GRAPHIMEDIC SA DE CV

Reference45 articles.

1. Yamaguchi T, Yamato M, Saotome K. First histologically confirmed case of a classic chordoma arisen in a precursor benign notochordal lesion: differential diagnosis of benign and malignant notocordal lesions. Skeletal Radiol. 2002; 31: 413-418.

2. Farshad M, Selman F, Burkhard MD, Müller D, Spirig JM. Partial sacrectomy with patient-specific osteotomy guides. NASSJ 2021; 8: 100090. Available in: https://doi.org/10.1016/j.xnsj.2021.100090

3. Tirabosco R, O\\\'Donell PG, Yamaguchi T. Conventional chordoma. In: WHO classification of tumours editorial board. Soft tissue and bone tumours. Lyon (France): International Agency for Research on Cancer; 2020. WHO classification of tumours series. 5th ed, vol. 3, 2020, 451-453. World Health Organization. Available in: https://publications.iarc.fr/588

4. Tirabosco R, Hameed M. Dedifferentiated chordoma. In: WHO Classification of tumours editorial board. Soft tissue and bone tumours. Lyon (France): International Agency for Research on Cancer; 2020. WHO classification of tumours series. 5th ed, volume 3, 2020, 454-455. World Health Organization. Available in: https://publications.iarc.fr/588

5. Nielsen GP, Dickson BC, Tirabosco R. Poorly differentiated chordoma. In: WHO Classification of Tumours Editorial Board. Soft tissue and bone tumours. Lyon (France): international agency for research on cancer; 2020. WHO classification of tumours series. 5th ed. volume 3, 2020, 456-457. World Health Organization. Available in: https://publications.iarc.fr/588

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