Askin's Tumor in the Chest Wall-a Rare Clinical Entity and Review of Literature
- PMID: 38741636
- PMCID: PMC11088598
- DOI: 10.1007/s13193-024-01921-1
Askin's Tumor in the Chest Wall-a Rare Clinical Entity and Review of Literature
Abstract
Askin tumors are the rare malignancy of neuroectodermal origin of the thoracic wall. Its prevalence is more in younger age group who present with vague symptoms leading to delayed diagnosis. We hereby present a case report of complex management of large chest wall tumor in a young boy and review the literature of this entity.
Keywords: IHC (immunohistochemistry); NACT (neoadjuvant chemotherapy); OS (overall survival); POD (postoperative day); SE/PPNETS (Ewing’s sarcoma/peripheral primitive neuroectodermal tumor); SUV (standard uptake value).
© The Author(s), under exclusive licence to Indian Association of Surgical Oncology 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
Conflict of interest statement
Conflict of InterestThe authors declare no competing interests.
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References
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- Askin FB, Rosai J, Sibley RK, Dehner LP, McAlister WH. Malignant small cell tumor of the thoracopulmonary region in childhood: a distinctive clinicopathologic entity of uncertain histogenesis. Cancer. 1979;43:2438–2451. doi: 10.1002/1097-0142(197906)43:6<2438::AID-CNCR2820430640>3.0.CO;2-9. - DOI - PubMed
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- Ushigome S, Machinami R, Sorensen PH (2002) Sarcoma/primitive neuroectodermal tumour. In: World Health Organization Classification of Tumors. Pathology and Genetics of Tumours of Soft Tissue and Bone. 1st ed; 298–300
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