Title of article
Secondary ALL after Successful Treatment of Ewingʹs Sarcoma: A Case Report
Author/Authors
Goudarzi Pour، Kourosh نويسنده Pediatric Congenital Hematologic Disorders Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran Goudarzi Pour, Kourosh , Alavi، Samin نويسنده , , Shamsian، Bibi-Shahin نويسنده , , Aghakhani، Roxana نويسنده Department of Pathology, Shahid Beheshti Medical University, Tehran, Iran. Aghakhani, Roxana , Arzanian، Mohammad Taghi نويسنده Department of Pediatrics, Division of Pediatric Oncology, Mofid Children Hospital, Shahid Beheshti University of Medical Sciences , , Hoseini Tavassol، Hesameddin نويسنده Pediatric Congenital Hematologic Disorders Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran Hoseini Tavassol, Hesameddin , Eydian، Zahra نويسنده Pediatric Congenital Hematologic Disorders Research Center, Shahid Beheshti Medical University, Tehran, Iran. Eydian, Zahra , Kazemi، Reyhaneh نويسنده Pediatric Congenital Hematologic Disorders Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran Kazemi, Reyhaneh
Issue Information
فصلنامه با شماره پیاپی 0 سال 2016
Pages
3
From page
236
To page
238
Abstract
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.
Journal title
International Journal of Hematology-Oncology and Stem Cell Research (IJHOSCR)
Serial Year
2016
Journal title
International Journal of Hematology-Oncology and Stem Cell Research (IJHOSCR)
Record number
2395883
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