Ewing sarcoma: A rare report from the Indian pediatric population

Authors

  • Dinesh Kumar G
  • Dinesh T
  • Benita S Raj
  • Daniel Sundar Singh

DOI:

https://doi.org/10.32677/ijcr.v8i10.3639

Keywords:

Bone tumor, Cancer, Children, Ewing Sarcoma, Hip, Indian Population, Round cell tumor

Abstract

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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Published

2024-01-29

Issue

Section

Case Report

How to Cite

Ewing sarcoma: A rare report from the Indian pediatric population. (2024). Indian Journal of Case Reports, 8(10), 319-321. https://doi.org/10.32677/ijcr.v8i10.3639

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