Trisomy 4, a new chromosomal abnormality in Waldenström's macroglobulinemia: A study of 39 cases [10]

Leukemia

Volumn 20, Issue 9, 2006, Pages 1634-1636

  Terre C ^a   Nguyen Khac, F ^b   Barin, C ^c   Mozziconacci, M J ^d   Eclache, V ^e   Leonard C ^f   Chapiro, E ^b   Farhat, H ^a   Bouyon, A ^a   Rousselot, P ^a   Choquet, S ^a   Spentchian, M ^a   Dubreuil, P ^d   Leblond, V ^b   Castaigne, S ^a  

^a CENTRE HOSPITALIER DE VERSAILLES   (France)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^c CHU BRETONNEAU   (France)

^d INSTITUT PAOLI CALMETTES   (France)

^e AVICENNE HOSPITAL   (France)

^f BICÊTRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN P53;

ANEUPLOIDY; CENTROMERE; CHROMOSOME 4; CHROMOSOME 6Q; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION 11; CHROMOSOME TRANSLOCATION 18; CLINICAL ARTICLE; CONTROLLED STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; INTERPHASE; LETTER; METAPHASE; NUMERICAL CHROMOSOME ABERRATION; PARTIAL TRISOMY 4; PATHOGENESIS; PRIORITY JOURNAL; TRISOMY; TRISOMY 18; TRISOMY 4; WALDENSTROEM MACROGLOBULINEMIA;

EID: 33747620495     PISSN: 08876924     EISSN: 14765551     Source Type: Journal    
DOI: 10.1038/sj.leu.2404314     Document Type: Letter

References (6)

1. Schop R, Kuehl W, Van Wier S, Ahmann G, Price-Troska T, Bailey R et al. Waldenström macroglobulinemia neoplastic cells lack immunoglobulin heavy chain locus translocations but have frequent 6q deletions. Blood 2002; 100: 2996-3001.
2. Avet-Loiseau H, Garand R, Lode L, Robillard N, Bataille R. 14q32 translocations discriminate IgM multiple myeloma from Waldenström macroglobulinemia. Semin Oncol 2003; 30: 153-155.
3. Hirase N, Miyamura T, Ishikura H, Yufu Y, Nishimura J, Nawata H. Primary macroglobulinemia with t(11;18)(q21;q21). Rinsho Ketsueki 1996; 37: 340-345.
4. Hirase N, Yufu Y, Abe Y, Muta K, Shiokawa S, Nawata H et al. Primary macroglobulinemia with t(11;18)(q21;q21). Cancer Genet Cytogenet 2000; 117: 113-117.
5. Schop RF, Jalal SM, Van Wier SA, Ahmann GJ, Bailey RJ, Kyle RA et al. Deletions of 17p13.1 and 13q14 are uncommon in Waldenström macroglobulinemia clonal cells and mostly seen at the time of disease progression. Cancer Genet Cytogenet 2002; 132: 55-60.
6. Rivera A, Li M, Beltran G, Krause J. Trisomy 4 as the sole cytogenetic abnormality in a Waldenström macroglobulinemia. Cancer Genet Cytogenet 2002; 133: 172-173.