Chronic eosinophilic leukemia and hypereosinophilic syndromes: Proposal for classification, literature review, and report of a case with a unique chromosomal abnormality

Cancer Genetics and Cytogenetics

Volumn 107, Issue 2, 1998, Pages 111-117

  Oliver, Jeffrey W ^a   Deol, Inderjit ^b   Morgan, David L ^a   Tonk, Vijay S ^a  

^a TEXAS TECH UNIVERSITY HEALTH SCIENCES CENTER SCHOOL OF MEDICINE   (United States)

^b Paul L Foster School of Medicine   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA INTERFERON; CYCLOSPORIN; HYDROXYUREA; PREDNISONE;

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 15; CLINICAL FEATURE; CONGESTIVE HEART FAILURE; DISEASE CLASSIFICATION; EOSINOPHILIC LEUKEMIA; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HYPEREOSINOPHILIC SYNDROME; KARYOTYPE; MALE; PRIORITY JOURNAL; TRISOMY;

ADULT; CHROMOSOMES, HUMAN, PAIR 15; CHRONIC DISEASE; HUMANS; HYPEREOSINOPHILIC SYNDROME; KARYOTYPING; MALE; TRISOMY;

EID: 0032402207     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(98)00099-5     Document Type: Article

References (49)

1. Chusid M.J., Dale D.C., West B.C., Wolff S.M. The hypereosinophilic syndrome. analysis of fourteen cases with review of the literature Medicine. 54:1975;1-27.
2. Seabright M (1971): A rapid banding technique for human chromosomes. Lancet ii:971-972.
3. Schwartz L.B. Hypereosinophilic syndrome. a review Virginia Med. 111:1984;350-355.
4. Flaum M.A., Schooley R.T., Fauci A.S., Gralnick H.R. A clinicopathologic correlation of the idiopathic hypereosinophilic syndrome. I. Hematologic manifestations. Blood. 58:1981;1012-1020.
5. Goldman J.M., Najfeld V., Th'ng K.H. Agar culture and chromosome analysis of eosinophilic leukaemia. J Clin Path. 28:1975;956-961.
6. Yoo T.J., Orman S.V., Patil S.R., Dorminey C., Needleman S., Rajtora D., Graves N., Ackerman L., Taylor W.W. Evolution to eosinophilic leukemia with a t(5;11) translocation in a patient with idiopathic hypereosinophilic syndrome. Cancer Genet Cytogenet. 11:1984;389-394.
7. Broustet A., Bernard P., Dachary D., David B., Marit G., Lacombe F., Issanchou A.M., Reiffers J. Acute eosinophilic leukemia with a translocation (10p+;11q-). Cancer Genet Cytogenet. 21:1986;327-333.
8. Schooley R.T., Flaum M.A., Gralnick H.R., Fauci A.S. A clinicopathologic correlation of the idiopathic hypereosinophilic syndrome. II. Clinical manifestations. Blood. 58:1981;1021-1026.
9. Spry C.J.F. The hypereosinophilic syndrome. Clinical features, laboratory findings and treatment Allergy. 37:1982;539-551.
10. Fauci A.S., Harley J.B., Roberts W.C., Ferrans V.J., Gralnick H.R., Bjornson B.H. The idiopathic hypereosinophilic syndrome. Clinical, pathophysiologic, and therapeutic considerations Ann Intern Med. 97:1982;78-92.
11. Weller P.F., Bubley G.J. The idiopathic hypereosinophilic syndrome. Blood. 83:1994;2759-2779.
12. Taylor C.G., Stasi R., Bastianelli C., Venditti A., Del Poeta G., Amadori S., Sargent J. Diagnosis and classification of the acute leukemias. Recent advances and controversial issues Hematopathol Molec Hematol. 10:1996;1-38.
13. Bain B.J. Eosinophilic leukaemias and the idiopathic hypereosinophilic syndrome. Br J Haematol. 95:1996;2-9.
14. Bitter M.A., Le Beau M.M., Larson R.A., Rosner M.C., Golomb H.M., Rowley J.D., Vardiman J.W. A morphologic and cytochemical study of acute myelomonocytic leukemia with abnormal marrow eosinophils associated with inv(16)(p13q22). Am J Clin Pathol. 81:1984;733-741.
15. D'Angelo G., Giardini C., Calvano D. Hyperleukocytosis with marked hypereosinophilia. Morphologic and cytochemical pathologic aspects of eosinophils. Eosinophilic leukaemia? Recenti Progressi Med. 86:1995;391-393.
16. Spry C.J.F. Eosinophils. A Comprehensive Review and Guide to the Scientific and Medical Literature. 1988;Oxford Medical Publication, Oxford.
17. Huang C.S., Gomez G.A., Kohno S.-I., Sokal J.E., Sandberg A.A. Chromosomes and causation of human cancer and leukemia. XXXIV. A case of "hypereosinophilic syndrome" with unusual cytogenetic findings in a chloroma, terminating in blastic transformation and CNS leukemia. Cancer. 44:1979;1284-1289.
18. Parreira L., De Castro J.T., Hibbin J.A., Marsh J.C.W., Marcus R.E., Brito Babapulle V., Spry C.J.F. Chromosome and cell culture studies in eosinophilic leukaemia. Br J Haematol. 62:1986;659-669.
19. Guitard A.M., Horschowski N., Mozziconacci M.J., Michel G., George F., Capodano A.M., Perrimond H. Hypereosinophilic syndrome in childhood. trisomy 8 and transformation to mixed acute leukaemia Nouv Rev Fr Hematol. 35:1993;555-559.
20. Peterson L.C., Parkin J.L., Arthur D.C., Brunning R.D. Acute basophilic leukemia. a clinical, morphologic, and cytogenetic study of eight cases Am J Clin Pathol. 96:1991;160-170.
21. Brunning R.D., McKenna R.W. Tumors of the Bone Marrow. Atlas of Tumor Pathology, 3rd series, fascicle 9. 1994;Armed Forces Institute of Pathology, Washington.
22. Goh K.O., Ho F.S.C., Tso S.C., Ma J. Is hypereosinophilic syndrome a malignant disease? Cancer. 55:1985;2395-2399.
23. Dewald G.W., Noel P., Dahl R.J., Spurbeck J.L. Chromosome abnormalities in malignant hematologic disorders. Mayo Clin Proc. 60:1985;675-689.
24. Wlodarska I., Mecucci C., Marynen P., Guo C., Franckx D., La Starza R., Aventin A., Bosly A., Martelli M.F., Cassiman J.J., Van den Berghe H. TEL gene is involved in myelodysplastic syndromes with either the typical t(5;12)(q33;p13) translocation or its variant t(10;12)(q24;p13). Blood. 85:1995;2848-2852.
25. Mitelman F., Panani A., Brandt L. Isochromosome 17 in a case of eosinophilic leukaemia. an abnormality common to eosinophilic and neutrophilic cells Scand J Haematol. 14:1975;308-312.
26. Da Silva M.A.P., Heerema N., Schwenk G.R., Hoffman R. Evidence for the clonal nature of hypereosinophilic syndrome. Cancer Genet Cytogenet. 32:1988;109-115.
27. Michel G., Thuret I., Capodano A.M., Scheiner C., Guitard A.M., Mozziconacci M.J., Fossat C., Perrimond H. Myelofibrosis in a child suffering from a hypereosinophilic syndrome with trisomy 8. response to corticotherapy Med Pediatr Oncol. 19:1991;62-65.
28. Malbrain M.L.N.G., Van Den Bergh H., Zachee P. 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 Br J Haematol. 92:1996;176-183.
29. Keene P., Mendelow B., Pinto M.R., Bezwoda W., MacDougall L., Falkson G., Ruff P., Bernstein R. Abnormalities of chromosome 12p13 and malignant proliferation of eosinophils. a nonrandom association Br J Haematol. 67:1987;25-31.
30. Fruehauf S., Fiehn C., Haas R., Doehner H., Hunstein W. Sustained remission of idiopathic hypereosinophilic syndrome following α-interferon therapy. Acta Haematol. 89:1993;91-93.
31. Bockenstedt P.L., Santinga J.T., Bolling S.F. α-Interferon treatment for idiopathic hypereosinophilic syndrome. Am J Hematol. 45:1994;248-251.
32. Zabel P., Schlaak M. Cyclosporin for hypereosinophilic syndrome. Ann Hematol. 62:1991;230-231.
33. Weinfeld A., Westin J., Swolin B. Ph1-negative eosinophilic leukaemia with trisomy 8. case report and review of cytogenetic studies Scand J Haematol. 18:1977;413-420.
34. Bitran J.D., Rowley J.D., Plapp F., Golomb H.M., Ultmann J.E. Chromosomal aneuploidy in a patient with hypereosinophilic syndrome. evidence for a malignant disease Am J Med. 63:1977;1010-1014.
35. Cabrol C. Chromosomal anomaly in eosinophilic leukemia. New Engl J Med. 301:1979;439.
36. Ellman L., Hammond D., Atkins L. Eosinophilia, chloromas and a chromosome abnormality in a patient with a myeloproliferative syndrome. Cancer. 43:1979;2410-2413.
37. Lonnqvist B., Gahrton G., Eriksson P., Friberg K., Zech L. Isochromosome 17 in a patient with a myeloproliferative disorder terminating in eosinophilic leukemia. Acta Med Scand. 206:1979;321-325.
38. Humphrey M.J., Hutter J.J., Tom W.W. Hypereosinophilia in a monosomy 7 myeloproliferative disorder in childhood. Am J Hematol. 11:1981;107-110.
39. Keneko Y., Kimpara H., Kawai S., Fujimoto T. 8;21 Chromosome translocation in eosinophilic leukemia. Cancer Genet Cytogenet. 9:1983;181-183.
40. Presti C., Ryan T., Armstrong W.F. Two-dimensional and doppler echocardiographic findings in hypereosinophilic syndrome. Am Heart J. 114:1987;172-175.
41. Mitter N.S., Weiskopf R.W. Unusual chromosome 7 aberrations in a case of eosinophilic myeloproliferative syndrome. Cancer Genet Cytogenet. 26:1987;209-212.
42. Darbyshire P.J., Shortland D., Swansbury G.J., Sadler J., Lawler S.D., Chessels J.M. A myeloproliferative disease in two infants associated with eosinophilia and chromosome t(1;5) translocation. Br J Haematol. 66:1987;483-486.
43. Harrington D.S., Peterson C., Ness M., Sanger W., Smith D.M., Vaughan W. Acute myelogenous leukemia with eosinophilic differentiation and trisomy-1. Am J Clin Pathol. 90:1988;464-469.
44. Fischkoff S.A., Testa J.R., Schiffer C.A. Acute eosinophilic leukemia with a (10;11) chromosomal translocation. Leukemia. 2:1988;394-397.
45. Needleman S.W., Mane S.M., Gutheil J.C., Kapil V., Heyman M.R., Testa J.R. Hypereosinophilic syndrome with evolution to myeloproliferative disorder. temporal relationship to loss of Y chromosome and c-N-ras activation Hematol Pathol. 4:1990;149-155.
46. Wolz D.E., Granato J.E., Giles H.R., Marks S.M., Grill H.P. A unique chromosomal abnormality in idiopathic hypereosinophilic syndrome presenting with cardiac involvement. Am Heart J. 126:1993;246-248.
47. Ribiero I., Carvalho I.R., Fontes M., Lima F., Matos R., Anderson B.A., Sousa Uva L. Eosinophilic leukaemia with trisomy 8 and double gammopathy. J Clin Pathol. 48:1993;672-673.
48. Sato H., Danbara M., Tamura M., Morita M. Eosinophilic leukaemia with a t(2;5)(p23;q35) translocation. Br J Haematol. 87:1994;404-406.
49. Gotic M., Radosevic-Radojkovic N., Ludoski M., Spasic P., Basara N., Avramovic D., Boskovic D., Rolovic Z. Eosinophilic leukemia with chromosomal aberration t(5;12)(q31;q13). an evidence of the existence of chronic eosinophilic leukemia as a distinct myeloproliferative entity Br J Haematol. 87(suppl 1):1994;168.