A novel recurrent chromosomal aberration involving chromosome 7 in childhood myelodysplastic syndrome

Cancer Genetics and Cytogenetics

Volumn 201, Issue 1, 2010, Pages 52-56

  Lizcova, Libuse ^a   Zemanova, Zuzana ^a   Malinova, Eva ^a   Jarosova, Marie ^b   Mejstrikova, Ester ^c   Smisek, Petr ^c   Pospisilova, Dagmar ^b   Stary, Jan ^c   Michalova, Kyra ^a  

^a CHARLES UNIVERSITY   (Czech Republic)

^b PALACKÝ UNIVERSITY   (Czech Republic)

^c UNIVERSITY HOSPITAL MOTOL   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

MERCAPTOPURINE;

ADOLESCENT; ANAMNESIS; APLASTIC ANEMIA; ARTICLE; BONE MARROW CELL; BONE MARROW TRANSPLANTATION; CASE REPORT; CHILD; CHROMOSOME 7; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME LOSS; CHROMOSOME MARKER; DIFFERENTIAL DIAGNOSIS; FEMALE; HUMAN; HUMAN CELL; MALE; MYELODYSPLASTIC SYNDROME; MYELOID LEUKEMIA; PRESCHOOL CHILD; PRIORITY JOURNAL;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 7; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; MYELODYSPLASTIC SYNDROMES;

EID: 77954649573     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2010.05.004     Document Type: Article

References (12)

1. Niemeyer C.M., Baumann I. Myelodysplastic syndrome in children and adolescence. Semin Hematol 2008, 45:60-70.
2. Elghetany M.T. Myelodysplastic syndromes in children: a critical review of issues in the diagnosis and classification of 887 cases from 13 published series. Arch Pathol Lab Med 2007, 131:1110-1116.
3. Hasle H., Alonzo T.A., Auvrignon A., Behar C., Chang M., Creutzig U., et al. Monosomy 7 and deletion 7q in children and adolescents with acute myeloid leukemia: an international retrospective study. Blood 2007, 109:4641-4647.
4. Kardos G., Baumann I., Passmore S.J., Locatelli F., Hasle H., Schultz K.R., et al. Refractory anemia in childhood: a retrospective analysis of 67 patients with particular reference to monosomy 7. Blood 2003, 102:1997-2003.
5. Heerema N.A., Nachman J.B., Sather H.N., La M.K., Hutchinson R., Lange B.J., et al. Deletion of 7p or monosomy 7 in pediatric acute lymphoblastic leukemia is an adverse prognostic factor: a report from the Children's Cancer Group. Leukemia 2004, 18:939-947.
6. Baurmann H., Cherif D., Berger R. Interphase cytogenetics by fluorescent in situ hybridization (FISH) for characterization of monosomy-7-associated myeloid disorders. Leukemia 1993, 7:384-391.
7. Gibbons B., Lillington D.M., Monard S., Young B.D., Cheung K.L., Lister T.A., Kearney L. Fluorescence in situ hybridisation studies to characterise complete and partial monosomy 7 in myeloid disorders. Genes Chromosomes Cancer 1994, 10:244-249.
8. Viguié F., Prigent Y., Ramond S., Baumelou E., Cadiou M., Dreyfus F., Zittoun R. Fluorescence in situ hybridization analysis of minute marker chromosomes in leukemia with monosomy 7. Leukemia 1995, 9:1154-1158.
9. Zamecnikova A. Small marker chromosome and monosomy 7 in a pediatric patient with MDS. Cancer Genet Cytogenet 2008, 180:163-164.
10. ISCN: An International System for Human Cytogenetic Nomenclature 2009, S.Karger, Basel. L.G. Shaffer, M.L. Slovak, L.J. Campbell (Eds.).
11. Baumann I., Niemeyer C.M., Bennett J.M., Shannon K. Childhood myelodysplastic syndrome. WHO Classification of Tumours of Heamapoietic and Lymphoid tissues 2008, IARC, Lyon, pp. 104-7. S.H. Swerdlow, E. Campo, N.L. Harris, E.S. Jaffe, S.A. Pileri, S.A. Stein, J. Thiele, J.W. Vardim (Eds.).
12. de la Chapelle A., Lahtinen R. Monosomy 7 predisposes to diabetes insipidus in leukaemia and myelodysplastic syndrome. Eur J Haematol 1987, 39:404-411.