Askin's tumor

Akin'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

  1. ↑ 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. PMID 222426.
  2. ↑ Coindre, J. M. (1993). "[Askin's tumor: a clinicopathologic entity?]". Annales De Pathologie. 13 (2): 139–140. ISSN 0242-6498. PMID 8363677.
  3. ↑ Benbrahim, Z; Arifi, S; Daoudi, K; Serraj, M; Amara, B; Benjelloun, MC; Mellas, N; El Mesbahi, O (22 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. PMID 23339634.
  4. ↑ Grünewald, Thomas G. P.; Cidre-Aranaz, Florencia; Surdez, Didier; Tomazou, Eleni M.; de Álava, Enrique; Kovar, Heinrich; Sorensen, Poul H.; Delattre, Olivier; Dirksen, Uta (2018-07-05). "Ewing sarcoma". Nature Reviews Disease Primers. 4 (1). doi:10.1038/s41572-018-0003-x. ISSN 2056-676X.
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