H. Van Dekken et al., Clonal analysis of a case of multifocal oesophageal (Barrett's) adenocarcinoma by comparative genomic hybridization, J PATHOLOGY, 188(3), 1999, pp. 263-266
Citations number
17
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Oesophageal adenocarcinomas arising in Barrett's epithelium occasionally pr
esent as multiple lesions. This could be due to either a multifocal present
ation of the same tumour, or different neoplasms arising simultaneously in
a dysplastic Barrett's oesophagus ('field cancerization'). This is a report
of the genetic analysis of multiple neoplastic sites in a Barrett's oesoph
agus with an extensive area of dysplasia. In addition, the dysplastic Barre
tt's epithelium was evaluated. For the genetic screening, comparative genom
ic hybridization (CGH) allowed evaluation of the whole genome of each speci
men. Five cancerous regions were selected and subsequently dissected from p
araffin-embedded tissue blocks. The use of archival materials enabled a tar
geted collection of representative tumour locations. Multiple genetic aberr
ations were detected by CGH in all cancer sites. Losses on 3p, 4, 7q, 18q,
and Y, as well as gains on 8q, 9q, 12p, 13q, 17q, 20p and X, were found in
each specimen. In four out of the five lesions, simultaneous losses on 9p,
15q, and 16q, with concomitant gains on 5p, 7q, and 10p, were disclosed by
CGH. Adjacent high-grade dysplastic Barrett's mucosa shared the losses on 3
p, 4, 7q, 9p, 18, and Y, as well as the gains on 5p, 7q, 13q, 17q, and X, t
hereby confirming its precursor status. Within this single and rare case of
multifocal Barrett's adenocarcinoma, a monoclonal genotype was present. Th
is must have been caused by an extensive outgrowth of a single tumour. Copy
right (C) 1999 John Wiley & Sons, Ltd.