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Chromosome studies in plasma cell leukemia and multiple myeloma in transformation

โœ Scribed by Philippe Jonveaux; Roland Berger


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
423 KB
Volume
4
Category
Article
ISSN
1045-2257

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โœฆ Synopsis


Abstract

Four patients with plasma cell leukemia (PCL) and two with multiple myeloma (MM) in transformation had complex numerical and structural chromosome abnormalities. From data published in the literature, the cytogenetic patterns of 46 cases of PCL or MM in the leukemic phase are compared with chromosomal abnormalities found in MM. Although the spectrum of chromosomal abnormalities is comparable in both diseases, the incidence of chromosome abnormalities is higher in PCL than in MM. Hypodiploidy with monosomies for chromosomes 13, 16, 17, and 18 is also more frequent in PCL than in MM. A mutation within the TP53 gene was detected in one of the three patients studied molecularly.


๐Ÿ“œ SIMILAR VOLUMES


Molecular cytogenetic abnormalities in m
โœ H. Avet-Loiseau; L.E. Andree-Ashley; D. Moore II; M.P. Mellerin; J. Feusner; R. ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 150 KB ๐Ÿ‘ 3 views

Comparative genomic hybridization (CGH) was used to identify recurrent regions of DNA sequence loss and gain in 21 multiple myeloma (MM) and plasma cell leukemia (PCL) primary tumor specimens and cell lines. Multiple regions of non-random sequence loss and gain were observed in 8/8 primary advanced