Atypical Chronic Myeloid Leukemia (aCML)

2008-06-01   Jesus M Hernandez  , Teresa Villaescusa  , Maryam Arefi  , Lucía López  , Juan L Garcia  

1.Unidad de Citogenetica Oncologica, Servicio de Hematologia, Hospital Universitario de Salamanca, Paseo San Vicente 58-182, 37007 Salamanca, Spain

Clinics and Pathology

Disease

aCML is a chronic myeloproliferative disorder with a clinical and hematological picture similar to chronic myelogenous leukemia (CML) but lacking Philadelphia chromosome and BCR - ABL or PDGFRBeta rearangements. Atypical CML is characterized by the combination of: 10-20% of immature granulocytes; marked granulocytic dysplasia and both less than 2% of basophils and less than 10% of monocytes.

Phenotype stem cell origin

Presumably a multipotential stem cell.

Epidemiology

ACML is a rare disorder of old adults. No predominance of sex. The incidence is not established.

Clinics

Anemic syndrome. Splenomegaly. Malaise.

Cytology

  • Peripheral blood: Leukocytosis with a high count of immature granulocytes. By definition monocytes are less than 10% and basophils less than 2%. Anemia is more frequent than thrombocytopenia.
  • Bone marow: Hypercellular with myelodysplastic features of the three series, most marked in granulocytic lineage. Blast cell infiltration ranges from 0% to 10%.

    • Treatment

    Hydroxyurea is indicated, although not curative, in old patients. Complete remission may be achieved after chemotherapy based on anthracyclin and citarabine (an acute myeloblastic leukemia therapy schedule). Allogeneic bone marrow transplantation is the only curative therapy for those patients who are eligible. Some cases may achieve a complete hematological response after interferon therapy.

    Prognosis

    The median survival is about 24 months with standart therapy. Some cases have a progression to acute myeloblastic leukemia.

    Genes Involved and Proteins

    Note
    The mechanisms of oncogenesis in aCML remains to be elucidated. In the last years some cases displaying rearrangement PDGFRb have been reported. Most of these cases showed PDGFRb / ETV6 fusion, but also a fusion with H4 gene (located at 10q22), have been described. A total of 8 different genes have been found fused to PDGFRb gene. The diagnosis of these cytogenetic abnormalities are critical since most these cases could achieve a complete cytogenetic response with imatinib therapy. The JAK2V617F activating tyrosine kinase mutation is unfrequent in aCML.

    Article Bibliography

    Pubmed IDLast YearTitleAuthors

    Summary

    Note

    The nosology of aCML is controversial. The FAB classification includes aCML in the group of chronic myeloid leukemias. The WHO classification has classified aCML in the group of myelodysplastic/myeloproliferative diseases.

    Citation

    Jesus M Hernandez ; Teresa Villaescusa ; Maryam Arefi ; Lucía López ; Juan L Garcia

    Atypical Chronic Myeloid Leukemia (aCML)

    Atlas Genet Cytogenet Oncol Haematol. 2008-06-01

    Online version: http://atlasgeneticsoncology.org/haematological/2117/case-report-explorer/css/lib/favicon/favicon-32x32.png

    Historical Card

    2001-09-01 Atypical Chronic Myeloid Leukemia (aCML) by  Norma C Gutierrez,Jesus M Hernandez 

    Unidad de Citogenetica Oncologica, Servicio de Hematologia, Hospital Universitario de Salamanca, Paseo San Vicente 58-182, 37007 Salamanca, Spain