| Literature DB >> 12353311 |
Naoaki Sato1, Tatsuo Furukawa, Masayoshi Masuko, Shigeo Hashimoto, Hidenobu Takahashi, Miyako Baba, Koichi Inano, Noriatsu Suzuki, Ken Toba, Ichiro Fuse, Yoshifusa Aizawa.
Abstract
We describe a patient with untreated essential thrombocythemia (ET) who developed microgranular variant of acute promyelocytic leukemia, 9 years after the initial diagnosis of ET. He achieved complete remission (CR) but relapsed 11 months later. After achieving the second CR, he received peripheral stem cell transplantation from his HLA complete-matched sibling. Five months after the transplantation, he relapsed again with meningeal infiltration of leukemic cells. In this paper, we review cases of promyelocytic transformation of myeloproliferative diseases (MPD) other than chronic myeloid leukemia (CML). To our knowledge, this is the first case of promyelocytic transformation of Philadelphia chromosome negative untreated ET, in whom both t(15;17) and PML-RAR alpha fusion were proven. Copyright 2002 Wiley-Liss, Inc.Entities:
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Year: 2002 PMID: 12353311 DOI: 10.1002/ajh.10195
Source DB: PubMed Journal: Am J Hematol ISSN: 0361-8609 Impact factor: 10.047