Ewing sarcoma: A rare report from the Indian pediatric population
DOI:
https://doi.org/10.32677/ijcr.v8i10.3639Keywords:
Bone tumor, Cancer, Children, Ewing Sarcoma, Hip, Indian Population, Round cell tumorAbstract
Ewing’s sarcomas are rare, aggressive tumors with a tendency toward recurrence following resection, and early metastasis. Although patients of younger or older age account for almost 30% of instances, peak incidences occur between the ages of 10 and 20. We, hereby, report the case of a 10-year-old girl who presented with a 3-month history of pain in her right hip that was unable to be relieved by non-steroidal anti-inflammatory medicine and physical therapy. On examination, bone marrow aspiration revealed that the infiltration of malignant small round blue cells was managed by anticancer therapy successfully.
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Copyright (c) 2022 Dinesh Kumar G, Dinesh. T, Benita S. Raj, Daniel Sundar Singh
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.