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Rev. méd. Chile ; 150(3): 397-401, mar. 2022. ilus, tab
Article Dans Espagnol | LILACS | ID: biblio-1409816

Résumé

BCR-ABL1 negative atypical chronic myeloid leukemia (aCML) is a rare type of myeloproliferative / myelodysplastic syndrome characterized by leukocytosis and proliferation of dysplastic neutrophilic precursors in the absence of positivity for the BCR-ABL1 fusion gene. We report a 66-year-old woman and a 57-year-old man with aCML, who initially presented with general malaise and weight loss, associated with anemia, thrombocytopenia, and leukocytosis with left shift and dysplasia in the neutrophil series. Both evolved unfavorably after admission and died a few days later due to multiple organ failure.


Sujets)
Humains , Mâle , Femelle , Adulte d'âge moyen , Sujet âgé , Thrombopénie , Leucémie myéloïde chronique BCR-ABL positive/diagnostic , Leucémie myéloïde chronique BCR-ABL positive/génétique , Leucémie myéloïde chronique atypique BCR-ABL négative/génétique , Hyperleucocytose
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