Abstract
Chronic myelogenous leukemia (CML) is a primary disorder of the bone marrow that leads to expansion of the granulocytic series, less commonly the megakaryocytic series, and infrequently the erythroid cells. As a result of the expansion of the elements of each of these series, characteristic signs and symptoms occur (see below). The disease has two distinct phases: one, in which essentially “normal” differentiation occurs, can be readily controlled by many chemotherapeutic agents; and an acute phase, which usually results in limited survival and cannot be readily controlled. In general, the disease is associated with a specific chromosonal abnormality, and studies of this have lead to a greater understanding of how CML evolves. CML is distinguished easily from acute granulocytic leukemia when the former is in the chronic phase. However, it may be indistinguishable from the latter when the disease presents as an acute leukemia.2,61 This chapter is a review of the clinical characteristics of the disorder, the studies of the Philadelphia chromosome (Ph1) that yield information about the nature of the disease, and the therapeutic options that are currently available.
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Arlin, Z.A. (1984). Philadelphia Chromosome-Positive Chronic Myelogenous Leukemia: Diagnosis and Treatment. In: Molander, D.W. (eds) Diseases of the Lymphatic System. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-5198-9_5
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DOI: https://doi.org/10.1007/978-1-4612-5198-9_5
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