| Literature DB >> 15218416 |
Aya Ogami1, Akira Morimoto, Shigeyoshi Hibi, Shinjiro Todo, Tohru Sugimoto, Kanako Mori, Toshihiko Imamura, Hiroyuki Ishida, Takao Yoshihara, Akihiro Iguchi, Masue Imaizumi, Shinsaku Imashuku.
Abstract
Of the several kinds of therapy-related leukemia, therapy-related acute promyelocytic leukemia (t-APL) is most closely associated with topoisomerase II inhibitor administration for treatment of malignancies in adults. Although rare in children, the majority of therapy-related malignancies have been etoposide-related APL associated with Langerhans cell histiocytosis. The authors describe the development of t-APL after chemotherapy administered for non-Hodgkin's lymphoma (NHL) in an 8-year-old girl. One month after cessation of the 3-year chemotherapy regimen of doxorubicin and other agents but not etoposide or radiotherapy, the patient was diagnosed with t-APL with positive PML-RARA molecular abnormality. The patient attained a complete remission following treatment with all-trans retinoic acid-containing chemotherapy. Thereafter, she successfully received hematopoietic stem cell transplantation from an HLA-matched sibling donor. Development of t-APL associated with NHL in children appears to be rare.Entities:
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Year: 2004 PMID: 15218416 DOI: 10.1097/00043426-200407000-00005
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289