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Presence of the bcr/abl rearrangement in a patient with chronic neutrophilic leukaemia.
  1. C Christopoulos,
  2. K Kottoris,
  3. V Mikraki,
  4. E Anevlavis
  1. First Department of Internal Medicine, Agia Olga Hospital, Athens, Greece.

    Abstract

    An 83 year old women presented with a myeloproliferative disorder involving the myeloid and megakaryocytic lines, and characterised by mature neutrophil leucocytosis. There was a high/normal neutrophil alkaline phosphatase activity and absence of the Philadelphia chromosome, features compatible with a diagnosis of chronic neutrophilic leukaemia (CNL). Southern blot analysis of the patient's DNA revealed the presence of the bcr/abl rearrangement. Combined with a previous report of detection of Ph1 chromosome in long term bone marrow cultures in a patient with CNL, this finding suggests that the bcr/abl hybrid gene might occasionally result in a myeloproliferative disorder with a phenotype closely resembling that of CNL.

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