Therapy-related acute megakaryoblastic leukemia in a lung cancer patient
Therapy-related AML (t-AML) is one of the newly expanded dis- ease entities in the 2008 WHO classification, accounting for 10- 20% of all cases of AML, and its incidence is increasing world- wide because of improved survival rates following treatment for other primary cancers [1, 2]. Acute megakaryo...
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Veröffentlicht in: | Annals of laboratory medicine 2014, 34(2), , pp.155-158 |
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Sprache: | eng |
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Zusammenfassung: | Therapy-related AML (t-AML) is one of the newly expanded dis- ease entities in the 2008 WHO classification, accounting for 10- 20% of all cases of AML, and its incidence is increasing world- wide because of improved survival rates following treatment for other primary cancers [1, 2]. Acute megakaryoblastic leukemia (AMKL) (M7) is the least common of the t-AML French-Ameri- can-British (FAB) subtypes, and only two such cases have been reported to date [3, 4], neither of which was in Korea. AMKL ac- counts for about 7-10% of childhood AML cases (frequently as- sociated with Down syndrome), but only about 1% of adult AML cases [5]. Here, we describe a rare case of therapy-related acute megakaryoblastic leukemia (t-AMKL) with chromosome 5 and 7 abnormalities that presented ten years after chemoradio- therapy in an elderly lung cancer patient. KCI Citation Count: 0 |
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ISSN: | 2234-3806 2234-3814 |
DOI: | 10.3343/alm.2014.34.2.155 |