M. Kasami et al., MONOCLONALITY IN FIBROADENOMAS WITH COMPLEX HISTOLOGY AND PHYLLODAL FEATURES, Breast cancer research and treatment, 50(2), 1998, pp. 185-191
Fibroadenoma is a common cause of benign breast masses in young women.
These women have a slightly increased risk of subsequent breast cance
r, particularly if their tumors have complex histologic patterns. We a
ssessed monoclonality in fibroadenomas and correlated the results with
histologic analysis. We performed a clonal analysis of 52 fibroadenom
as from 43 patients using X-chromosome inactivation studies. The cases
included fibroadenomas with complex and simple histology. Areas exami
ned were predominantly stroma but epithelium was also present. DNA was
isolated from paraffin-embedded tissue and was subjected to polymeras
e chain reaction amplification of the human androgen receptor gene wit
h and without predigestion of the DNA with Hha 1. If a monoclonal proc
ess was identified, the epithelial and stromal components were subsequ
ently microdissected and reanalyzed. 36/43 (83.7%) women were heterozy
gous. We studied 45 tumors in these 36 informative women. 1/20 (5% com
plex fibroadenomas and 1/25 (4%) simple fibroadenomas were monoclonal.
The epithelial component of both monoclonal fibroadenomas was polyclo
nal. The one monoclonal simple fibroadenoma was also the only one with
mixed features to contain a phyllodes component. In this case, monocl
onality was found in the stroma of both the fibroadenoma and phyllodes
regions. Monoclonality has been previously associated with phyllodes
phenotype, but not with fibroadenomas, except for 3 fibroadenomas that
recurred as phyllodes tumor. We report that monoclonality may also be
seen occasionally in complex fibroadenomas, and was found in a tumors
with mixed fibroadenoma/phyllodes features without clinical recurrenc
e for 4 years.