z-logo
Premium
Trisomy 20 is a primary chromosome aberration in desmoid tumors
Author(s) -
Mertens Fredrik,
Willén Helena,
Rydholm Anders,
Brosjö Otte,
Carlén Birgitta,
Mitelman Felix,
Mandahl Nils
Publication year - 1995
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.2910630412
Subject(s) - trisomy , supernumerary , biology , chromosome , pathology , aneuploidy , karyotype , chromosome aberration , autosome , marker chromosome , genetics , medicine , anatomy , gene
Chdtogenetic analysis revealed trisomy 20 in 4 desmoid tumors: in 2 cases as the sole aberration, in hd together with +X, ‐Y and −13 and in I with +8 and a supernumerary marker chromosome. Our findings indicate that gain of chromosome 20 is an early event in the development of a large subset of desmoid tumors and that it is as frequent as +8, the only consistent chromosomal change previously reported in this tumor type. The non‐random occurrence of trisomies 8 and 20 in desmoid tumors indicates shared pathogenetic mechanisms with infantile fibrosarcoma, a fibrous tissue tumor characterized by various combinations of trisomies for chromosomes 8, 11, 17 and 20.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here