Cytogenetic study of 14 thyroid nodular hyperplasias revealed a hyperd
iploid karyotype in two cases (14%) and a normal chromosomal complemen
t in the remaining cases. Some of the numerical alterations found were
identical to the ones considered characteristic of a subset of thyroi
d adenomas (+5, +7, +9, +12, +14, and +16). Our findings suggest that
the cytogenetic events involved in the pathogenesis of thyroid hyperpl
astic lesions and benign tumors may be closely related, which supports
the hypothesis of a biologic ''continuum'' between these two types of
lesions.