We report the cytogenetic and histopathological findings in a 7-year-o
ld-female child with an intranasal tumor that is most consistent with
a parachordoma. Karyotypic analysis of the tumor revealed clonal numer
ical and str structural chromosome abnormalities. Seven cells displaye
d recurrent changes: der(2)t(2:4), del(3q), and the loss of chromosome
s 9, 10, 20, and 22. Four cells showed a loss of chromosome 17. To the
best of our knowledge, these are the first clonal chromosome abnormal
ities described in parachordoma. (C) Elsevier Science Inc., 1998.