Askin's tumor is a rare, primitive neuroectodermal tumor which arises from the soft tissues of the chest wall, particularly of the paravertebral region.[1][2] It was first described by Askin et al. in 1979.[3] Askin's tumor is now recognized as part of the Ewing's sarcoma family of tumors.[4] This neoplasm tended to recur locally, but did not seem to disseminate as widely as some of the other small cell tumors of childhood such as rhabdomyosarcoma or neuroblastoma.
References edit
- ^ Askin FB, Rosai J, Sibley RK, Dehner LP, McAlister WH (June 1979). "Malignant small cell tumor of the thoracopulmonary region in childhood: a distinctive clinicopathologic entity of uncertain histogenesis". Cancer. 43 (6): 2438–51. doi:10.1002/1097-0142(197906)43:6<2438::AID-CNCR2820430640>3.0.CO;2-9. PMID 222426.
- ^ Coindre JM (1993). "[Askin's tumor: a clinicopathologic entity?]". Annales de Pathologie. 13 (2): 139–40. PMID 8363677.
- ^ Benbrahim Z, Arifi S, Daoudi K, Serraj M, Amara B, Benjelloun MC, et al. (January 2013). "Askin's tumor: a case report and literature review". World Journal of Surgical Oncology. 11: 10. doi:10.1186/1477-7819-11-10. PMC 3556149. PMID 23339634.
- ^ Grünewald TG, Cidre-Aranaz F, Surdez D, Tomazou EM, de Álava E, Kovar H, et al. (July 2018). "Ewing sarcoma". Nature Reviews. Disease Primers. 4 (1): 5. doi:10.1038/s41572-018-0003-x. PMID 29977059. S2CID 49571421.
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