Pediatrics & Neonatology
Volume 50, Issue 5 , Pages 239-244, October 2009

Early Development of Acute Myeloid Leukemia Following Treatment of Osteosarcoma: A Case Report and Review of the Literature

  • Yu-Mei Shen

      Affiliations

    • Department of Pediatrics, Hsin Chu General Hospital, Hsinchu, Taiwan
  • ,
  • Giun-Yi Hung

      Affiliations

    • Department of Pediatrics, Taipei Veterans General Hospital, Taipei, Taiwan
    • National Yang-Ming University School of Medicine, Taipei, Taiwan
    • Corresponding Author InformationCorresponding author. Department of Pediatrics, Taipei Veterans General Hospital, 201, Section 2, Shih-Pai Road, Taipei 112, Taiwan
  • ,
  • Hsiu-Ju Yen

      Affiliations

    • Department of Pediatrics, Taipei Veterans General Hospital, Taipei, Taiwan
    • National Yang-Ming University School of Medicine, Taipei, Taiwan
  • ,
  • Ming-Yun Hsieh

      Affiliations

    • Department of Pediatrics, Taipei Veterans General Hospital, Taipei, Taiwan
    • National Yang-Ming University School of Medicine, Taipei, Taiwan
  • ,
  • Te-Kuei Hsieh

      Affiliations

    • Department of Pediatrics, Hsin Chu General Hospital, Hsinchu, Taiwan

Received 14 August 2008; received in revised form 13 January 2009; accepted 14 March 2009.

We report a case of treatment-related acute myeloid leukemia (t-AML) in a 16-year-old male following treatment for osteosarcoma (OS). He had been treated with a protocol comprising neoadjuvant chemotherapy, definitive surgery with wide excision and adjuvant chemotherapy for OS. Four months after completion of the treatment, a routine hemogram showed hyperleukocytosis with 90% blasts. Bone marrow aspirate and a chromosomal analysis disclosed acute myeloid leukemia (AML), M5b with 46, XY, t(11;19)(q23;p13.3). The t-AML was characterized by early development (just 4 months after completion of chemotherapy for OS) and generalized leukemia cutis. The patient received an alkylating agent (ifosfamide) and DNA topoisomerase II-targeted drugs (etoposide and doxorubicin). In terms of latency, cytogenetics, and presentation, DNA topoisomerase II-targeted drug-related leukemia seemed likely for this patient. Clinically, his leukemia cutis had developed during a nadir in white blood cell count after the first induction of chemotherapy for AML. The rapid progression and its refractoriness to chemotherapy were poor prognostic signs.

Key Words:  chemotherapy , osteosarcoma , secondary leukemia

No full text is available. To read the body of this article, please view the PDF online.

 

PII: S1875-9572(09)60070-X

doi:10.1016/S1875-9572(09)60070-X

Pediatrics & Neonatology
Volume 50, Issue 5 , Pages 239-244, October 2009