“…7 Other, earlier case reports that purportedly described patients presenting with initial Ph(À) ALL diagnoses, followed by CML being detected at a later time, are questionable because of the limitations in ancillary techniques available for a complete workup; 8 lack of cytogenetic information at the time of ALL diagnosis; 9 questionable diagnosis of CML, due to lack of the characteristic t(9;22) translocation; 10,11 and/or the presence of a Ph chromosome at the time of ALL diagnosis, which favors an interpretation of lymphoblastic BP CML (rather than de novo ALL). 12,13 CML can occur as a secondary neoplasm following exposure to radiation and/or chemotherapy. Of 33 published cases of therapy-related CML, 14,15 the majority occurred in adults with a history of classical Hodgkin lymphoma (median age, 43 years; range: 11-70 years).…”