Abstract |
Dermatofibrosarcoma protuberans (DFSP) presents with characteristic cytogenetic features such as reciprocal t(17;22)(q22;q13) or, more commonly, supernumerary ring chromosomes containing sequences from chromosomes 17 and 22. Here, we report the identification of a novel abnormality in a 43-year-old woman with DFSP. Cytogenetic analysis of tumor cells showed the presence of a supernumerary ring chromosome as the sole anomaly. Amplification of 8q11.2 approximately qter and 17q21 approximately qter sequences was confirmed by comparative genomic hybridization (CGH); the present case apparently lacked amplification of chromosome 22. To our knowledge, this is the first case indicating that the ring chromosome in DFSP is possibly associated with amplified material from chromosomes 8 and 17.
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Authors | J Nishio, H Iwasaki, Y Ohjimi, M Ishiguro, T Isayama, M Naito, Y Kaneko, M Kikuchi |
Journal | Cancer genetics and cytogenetics
(Cancer Genet Cytogenet)
Vol. 129
Issue 2
Pg. 102-6
(Sep 2001)
ISSN: 0165-4608 [Print] United States |
PMID | 11566338
(Publication Type: Case Reports, Journal Article)
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Topics |
- Adult
- Chromosome Aberrations
(diagnosis, genetics)
- Chromosome Disorders
- Chromosomes, Human, Pair 17
(genetics)
- Chromosomes, Human, Pair 8
(genetics)
- Dermatofibrosarcoma
(genetics, pathology)
- Female
- Humans
- In Situ Hybridization, Fluorescence
- Karyotyping
- Metaphase
- Ring Chromosomes
- Skin Neoplasms
(genetics, pathology)
- Tumor Cells, Cultured
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