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A second field metachronous Merkel cell carcinoma of the lip and the palatine tonsil confirmed by microarray-based comparative genomic hybridisation
Authors:Judit?Nagy,Liliána?Z.?Fehér,István?Sonkodi,József?Lesznyák,Béla?Iványi,László?G.?Puskás  author-information"  >  author-information__contact u-icon-before"  >  mailto:pusi@brc.hu"   title="  pusi@brc.hu"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Department of Oral Medicine, Department of Dentistry and Oral Surgery, University of Szeged, Faculty of Medicine, Szeged, Hungary;(2) Laboratory of Functional Genomics, Biological Research Centre, Hungarian Academy of Sciences, P.O. Box 521, 6701 Szeged , Hungary;(3) Department of Histopathology, Bács-Kiskun County Hospital, Kecskemét, Hungary;(4) Department of Pathology, University of Szeged, Szeged, Hungary
Abstract:Merkel cell carcinoma was diagnosed in a 79-year-old Caucasian woman. The tumour was localised to the upper lip and was in stage T2. After successful cryosurgery and a 7-year tumour-free period, a new tumour developed in her palatine tonsil. Histologically and immunohistochemically, this resembled the tumour in the lip. The regional lymph nodes were devoid of metastasis. The paraffin-embedded material of the two tumours and the unaffected lymphatic tissue were analysed with DNA microarrays for comparative genomic hybridisation to assess the genetic relationship of the tumours. In both tumours, regions on 2p and 10p were commonly over-represented, while 41 regions on chromosomes 1–4, 6, 8–9, 11 and 14–22 were commonly under-represented. Chromosomes 1, 3, 4, 16–18 and X were most frequently involved in the DNA losses. In gene copy numbers in the two tumours, 31 chromosome locations were found to be differently affected. The partly similar and partly different molecular patterns indicated a genetic relationship between the tumours and excluded the possibility that the tonsillar tumour was a metastasis. The findings suggest that a genetically altered field was the reason for the development of the tonsillar cancer; thus, it can be regarded pathogenetically as a second field tumour.
Keywords:Merkel cell carcinoma  Second field tumour  Comparative genomic hybridisation  DNA microarray  Chromosome imbalances
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