Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12
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Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12. / Nilsson, Malin A; Domanski, Henryk; Mertens, Fredrik; Mandahl, Nils.
I: Oncology Reports, Vol. 13, Nr. 4, 04.2005, s. 649-652.Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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T1 - Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12
AU - Nilsson, Malin A
AU - Domanski, Henryk
AU - Mertens, Fredrik
AU - Mandahl, Nils
N1 - The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Division of Clinical Genetics (013022003), Pathology, (Lund) (013030000)
PY - 2005/4
Y1 - 2005/4
N2 - Atypical lipomatous tumor (ALT), an intermediate malignant neoplasm of soft tissues, is characterized by the presence of supernumerary ring and giant marker chromosomes. These supernumerary chromosomes consistently contain amplified 12q-material in association with amplified segments from a variety of other chromosomes. However, a few cases of ALT with other types of chromosomal rearrangements have been reported earlier. We report on new types of structural aberrations in a case of ALT. In a pseudodiploid karyotype, there were two aberrant chromosomes, both consisting of alternating chromosome 8 and 12 sequences as shown by multicolor fluorescence in situ hybridization (FISH). The complex rearrangement was not only the result of multiple breaks and reunions of these chromosomes, but was also associated with a gain of chromosome 12 sequences. FISH analyses revealed that the number of MDM2 signals was slightly elevated (median, 5). There were three intact copies of HMGA2 and one additional copy of the 5' part of the gene. These findings are consistent with previous reports that the ALT phenotype may be associated with a low or moderate level of gene amplification, whereas truncation of HMGA2 has been observed in both ALTs and benign lipomas. The aberrations in the present case were stable, although rare cells with higher MDM2 copy numbers were detected. Whether ALTs with these types of aberrations have a lower risk of tumor progression than ALTs with the notoriously mitotically unstable ring and giant marker chromosomes remains to be investigated.
AB - Atypical lipomatous tumor (ALT), an intermediate malignant neoplasm of soft tissues, is characterized by the presence of supernumerary ring and giant marker chromosomes. These supernumerary chromosomes consistently contain amplified 12q-material in association with amplified segments from a variety of other chromosomes. However, a few cases of ALT with other types of chromosomal rearrangements have been reported earlier. We report on new types of structural aberrations in a case of ALT. In a pseudodiploid karyotype, there were two aberrant chromosomes, both consisting of alternating chromosome 8 and 12 sequences as shown by multicolor fluorescence in situ hybridization (FISH). The complex rearrangement was not only the result of multiple breaks and reunions of these chromosomes, but was also associated with a gain of chromosome 12 sequences. FISH analyses revealed that the number of MDM2 signals was slightly elevated (median, 5). There were three intact copies of HMGA2 and one additional copy of the 5' part of the gene. These findings are consistent with previous reports that the ALT phenotype may be associated with a low or moderate level of gene amplification, whereas truncation of HMGA2 has been observed in both ALTs and benign lipomas. The aberrations in the present case were stable, although rare cells with higher MDM2 copy numbers were detected. Whether ALTs with these types of aberrations have a lower risk of tumor progression than ALTs with the notoriously mitotically unstable ring and giant marker chromosomes remains to be investigated.
KW - Biopsy
KW - Chromosome Aberrations
KW - Chromosome Banding
KW - Chromosomes
KW - Chromosomes, Human, Pair 12
KW - Chromosomes, Human, Pair 8
KW - Disease Progression
KW - Female
KW - Humans
KW - In Situ Hybridization, Fluorescence
KW - Interphase
KW - Karyotyping
KW - Lipoma
KW - Middle Aged
KW - Neoplasms, Adipose Tissue
KW - Phenotype
KW - Case Reports
KW - Journal Article
KW - Research Support, Non-U.S. Gov't
U2 - 10.3892/or.13.4.649
DO - 10.3892/or.13.4.649
M3 - Article
C2 - 15756437
VL - 13
SP - 649
EP - 652
JO - Oncology Reports
JF - Oncology Reports
SN - 1791-2431
IS - 4
ER -