Abstrait
Comme les autres syndromes myéloprolifératifs,la leucémie myéloïde chronique (LMC)est un processus monoclonal résultant de l’atteinte d’une cellule souche. C ’est essentiellement la lignée granuleuse qui y prolifère. Elle est caractérisée par une aberration acquise du caryotype : la translocation (9 ;22)ou chromosome Philadelphie (Ph1), se traduisant par la juxtaposition anormale des gènes abl du chromosome 9 et bcr du chromosome 22 (1).Il s ’agit du premier exemple de signature chromosomique et moléculaire mis en évidence parmi les cancers humains.
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Carli, P.M., Troussard, X., Maarouf, N., Maynadié, M. (2007). Leucémie myéloïde chronique. In: Grosclaude, P., et al. Survie des patients atteints de cancer en France. Springer, Paris. https://doi.org/10.1007/978-2-287-39310-5_46
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DOI: https://doi.org/10.1007/978-2-287-39310-5_46
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