THYROID NODULAR HYPERPLASIA - CHROMOSOMAL STUDIES IN 14 CASES

Citation
L. Roque et al., THYROID NODULAR HYPERPLASIA - CHROMOSOMAL STUDIES IN 14 CASES, Cancer genetics and cytogenetics, 69(1), 1993, pp. 31-34
Citations number
24
Categorie Soggetti
Oncology,"Genetics & Heredity
ISSN journal
01654608
Volume
69
Issue
1
Year of publication
1993
Pages
31 - 34
Database
ISI
SICI code
0165-4608(1993)69:1<31:TNH-CS>2.0.ZU;2-U
Abstract
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.