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Translocation t(11;14)(q13;q32) is the hallmark of IgM, IgE, and nonsecretory multiple myeloma variants
被引:126
|作者:
Avet-Loiseau, H
Garand, R
Lodé, L
Harousseau, JL
Bataille, R
机构:
[1] Univ Hosp Nantes, Hematol Lab, Nantes, France
[2] Univ Hosp Nantes, Dept Clin Hematol, Nantes, France
来源:
关键词:
D O I:
10.1182/blood-2002-08-2436
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
In an attempt to address the issue of cytogenetic features of multiple myeloma (MM) variants, we have analyzed a series of 8 IgM, 9 IgD, 2 IgE, and 14 nonsecretory (NS) MM cases using fluorescence in situ hybridization. A very high incidence (83%) of t(11;14)(q13;q32) was detected in the IgM (7 of 8), IgE (2 of 2), and NS (11 of 14) MM cases, but not in the IgD cases (2 of 9). Of note, no t(4;l 4) was observed in this cohort of patients. This increased incidence of t(11;14) was associated with 2 dominant features in these variants, namely, a "lymphoplasmacytic" presentation mainly in IgM MM and a lower secreting capacity in the others, 2 features previously associated with t(11;14). Of major interest, t(11;14) was never observed in Waldenstrom macroglobullnemia or in IgG/IgA "lymphoplasmacytic" lymphomas. Thus, for unknown masons, t(11;14) is the hallmark of IgM, IgE, and NS MM, (but not IgD MM), with a 5-fold increase of its incidence compared to that of IgG and IgA MM.
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页码:1570 / 1571
页数:2
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