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Résumé La maladie de Waldenström est un syndrome lymphoprolifératif B caractérisé par une infiltration médullaire par des cellules lymphoplasmocytaires monotypiques et une IgM monoclonale sérique. Les manifestations cliniques et les anomalies biologiques sont liées à l’infiltration tumorale aux spécificités physiques et à l’activité anticorps de l’immunoglobuline monoclonale. Une prise en charge multidisciplinaire...
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