secondary all after successful treatment of ewing's sarcoma: a case report

نویسندگان

kourosh goudarzi pour pediatric congenital hematologic disorders research center, shahid beheshti university of medical sciences, tehran, iran

samin alavi pediatric congenital hematologic disorders research center, shahid beheshti university of medical sciences, tehran, iran

shahin shamsian pediatric congenital hematologic disorders research center, shahid beheshti university of medical sciences, tehran, iran

roxana aghakhani pediatric congenital hematologic disorders research center, shahid beheshti university of medical sciences, tehran, iran

چکیده

treatment with intensification of chemotherapy using alkylating agents and topoisomerase ii inhibitors and radiotherapy has improved the outcome of patients with solid tumors such as ewing’s sarcoma. however, there are several reports of secondary malignancy following treatment of these tumors. in this article, we describe a 12 years old girl with all who had ewing’s sarcoma when she was 8 years old and underwent successful treatment but after two and half years at 12 years old, she came back with pallor and muscular pain.

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عنوان ژورنال:
international journal of hematology-oncology and stem cell research

جلد ۱۰، شماره ۴، صفحات ۲۳۶-۲۳۸

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