Although pituitary adenomas are among the most frequent intracranial neopla
sms, only very few have been cytogenetically analyzed. We have short-term c
ultured and karyotyped 28 consecutive pituitary adenomas (16 clinically non
functioning adenomas and 12 clinically functioning adenomas), finding a nor
mal karyotype in 22, whereas 6 had clonal chromosome aberrations (5 nonfunc
tioning pituitary adenomas and 1 prolactinoma). The abnormal karyotypes wer
e relatively simple. Most anomalies were numerical, with a structural rearr
angement, t(6;19), being found in only one tumor. The most common aberratio
ns were trisomy 7 (3 adenomas), trisomy 9 (2 adenomas), trisomy 12 (2 adeno
mas), trisomy 20 (2 adenomas) and loss and gain in 2 separate clones of one
X chromosome (2 adenomas). (C) Elsevier Science Inc., 1999 All rights rese
rved.