Eosinophilic leukemia associated with t(2;5)(p23;q31)

Cancer Genetics and Cytogenetics

Volumn 133, Issue 2, 2002, Pages 164-167

  Lepretre, Stéphane ^a   Jardin, Fabrice ^a   Buchonnet, Gérard ^b   Lenain, Pascal ^a   Stamatoullas, Aspasia ^a   Kupfer, Ingrid ^b   Courville, Philippe ^b   Callat, Marie Paule ^b   Contentin, Nathalie ^a   Bastard, Christian ^a,c   Tilly, Hervé ^a,c  

^a CENTRE HENRI BECQUEREL   (France)

^b ROUEN UNIVERSITY HOSPITAL   (France)

^c EMI 9903   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ACUTE LYMPHOCYTIC LEUKEMIA; ADULT; ARTICLE; BONE MARROW BIOPSY; BONE MARROW CELL; CASE REPORT; CHROMOSOME 2; CHROMOSOME 5; CHROMOSOME ANALYSIS; CHROMOSOME TRANSLOCATION; CHRONIC MYELOID LEUKEMIA; CONTROLLED STUDY; DIFFERENTIAL DIAGNOSIS; DISEASE ASSOCIATION; EOSINOPHILIA; EOSINOPHILIC LEUKEMIA; HEPATOSPLENOMEGALY; HUMAN; HUMAN TISSUE; HYPEREOSINOPHILIC SYNDROME; MALE; MALIGNANT NEOPLASTIC DISEASE; MYELODYSPLASTIC SYNDROME; PANCYTOPENIA; PRIORITY JOURNAL;

BONE MARROW; CHROMOSOMES, HUMAN, PAIR 2; CHROMOSOMES, HUMAN, PAIR 5; EOSINOPHILS; HUMANS; HYPEREOSINOPHILIC SYNDROME; KARYOTYPING; MALE; MIDDLE AGED; TRANSLOCATION, GENETIC;

EID: 18344378773     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(01)00590-8     Document Type: Article

References (11)

1. The hypereosinophilic syndrome; analysis of 14 cases with review of the literature
2. The idiopathic hypereosinophilic syndrome
3. Eosinophilic leukemia and the idiopathic hypereosinophilic syndrome
4. Interleukin-5, eosinophils, and disease
5. Association of an inversion of chromosome 16 with abnormal marrow eosinophils in acute myelomonocytic leukemia ; a unique cytogenetic-clinico-pathological association
6. Clonal eosinophilic disorder and the hypereosinophilic syndrome
7. Eosinophilic leukaemia with a t(2;5)(p23;q35) translocation
8. Eosinophilic leukaemia with an abnormality of 5q31, the site of the IL-5 gene
9. Abnormalities of chromosome 12p13 and malignant proliferation of eosinophils; a nonrandom association
10. Further evidence for the clonal nature of the idiopathic hypereosinophilic syndrome; complete haematological and cytogenetic remission induced by interferon-alpha in a case with a unique chromosomal abnormality
11. Clinical and cytogenetic remission induced by interferon-α in a patient with chronic eosinophilic leukemia associated with a unique t(3;9;5) translocation