Curr Health Sci J, vol. 46, no. 2, 2020

Ewing Sarcoma of Fibula: A Pediatric Case of Disease Regression and Bone Regeneration. Case Report and Literature Review

[Case Report]

C.V. STRIMBU(1), A.B. DEACANU(1), A.C. ESANU(1), A.E. LUCA(1), S.N. CRACANA(2)


(1)”Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania,
(2)Department of Pathology, Colentina Clinical Hospital, Bucharest, Romania


Abstract:

Ewing’s sarcoma is a rare type of bone malignancy that occurs mostly in the bones of the pelvis and the limbs. We report a case of Ewing’s sarcoma developed in the peroneal bone of a 10-year-old boy, with a severe affectation of the bone and pulmonary metastasis. Chemotherapy was administered to the patient. Approximately two years after first presentation, radiological exams indicated a nearly complete regenerated fibula and PET-CT scan indicated an inactive right lung mass. This case showed the incredible potency of recovery in pediatric patients and highlights the need for a personalized approach in pediatric orthopedic oncology.


Keywords:
Ewing sarcoma, fibula, bone tumor, childhood cancer, pulmonary metastasis



Corresponding:
Strimbu Codrut Vlad, "Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania, e-mail: vlad.strimbu@stud.umfcd.ro


DOI 10.12865/CHSJ.46.02.17 - Download PDF