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Detection of chromosome 11 alterations in blood and bone marrow by interphase cytogenetics in mantle cell lymphoma

✍ Scribed by Emanuele Zucca; Gianni Soldati; Brigitte Schlegelberger; Mark J. Booth; Klaus Weber-Matthiesen; Franco Cavalli; Finbarr E. Cotter


Book ID
114714452
Publisher
John Wiley and Sons
Year
1995
Tongue
English
Weight
344 KB
Volume
89
Category
Article
ISSN
0007-1048

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Detection of t(11;14) using interphase m
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The chromosomal translocation t(11;14)(q13;q32) fuses the IGH and CCND1 genes and leads to cyclin D1 overexpression. This genetic abnormality is the hallmark of mantle cell lymphoma (MCL), but is also found in some cases of atypical chronic lymphocytic leukemia (CLL), characterized by a poor outcome

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## BACKGROUND. The cytomorphologic diagnosis of mantle cell lymphoma (MCL) can be difficult and requires ancillary studies for accurate subclassification. More than 95% of MCLs are known to carry the t(11;14) chromosomal translocation. However, traditional cytogenetic studies on cytologic material