N. Mandahl et al., NONRANDOM SECONDARY CHROMOSOME-ABERRATIONS IN SYNOVIAL SARCOMAS WITH T(X-18), International journal of oncology, 7(3), 1995, pp. 495-499
Thirty samples from 19 patients with synovial sarcoma were analyzed cy
togenetically after short-term culturing. Thirteen samples were from p
rimary tumors, 11 from local recurrences, and six from distant metasta
ses. All samples showed the characteristic aberration t(X;18)(p11;q11)
or variants thereof; 23 samples had additional numerical and/or struc
tural changes. Including the present cases, chromosome aberrations hav
e been reported in 74 synovial sarcomas, 50 of which have had secondar
y aberrations in addition to t(X;18). No secondary structural aberrati
on was recurrent. The most common numerical changes were +7, +8, +12 (
10 cases each), -3, +9, +21 (7 cases each), +2, -14, -17 (6 cases each
), +4, -11, +15, and -22 (5 cases each). Unbalanced stuctural aberrati
ons led to loss of 3p and 17p in six cases, each with loss of bands 3p
21 and 17p13, respectively, in common. Most monosomies and trisomies s
eemed to occur at similar frequencies in primary, recurrent, and metas
tatic tumors. The only exceptions were +2, which was never seen in a p
rimary tumor, and +8, which was never found in any metastatic lesion.