Ali Dastranj Tabrizi
1, Morteza Ghojazadeh
2*, Hanieh Thagizadeh Anvar
1, Amir Vahedi
1, Siamak Naji
3, Elmira Mostafidi
1, Siamak Berenjian
11 Women's Reproductive Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
2 Liver and Gastrointestinal Disease Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
3 Pathology Department, Urmieh University of Medical Sciences, Urmieh, Iran.
Abstract
Purpose: To
assess the immunohistochemical profile of the atypical nuclei in leiomyoma with
bizarre nuclei and compare with benign and malignant counterparts.
Methods: 26
cases of uterine smooth muscle tumors including 12 leiomyosarcoma(LMS), 10
leiomyoma with bizarre nuclei (LBN) and 4 smooth muscle tumor with uncertain
malignant potential (STUMP) were selected using whole tissue sections for this
study and analysis. Six cases of ordinary leiomyoma were included as benign
control group. All representative section were stained for P53, Ki67 , estrogen
receptor and progestrone receptor. Analysis was carried out using SPSS 16.0 for
windows software.
Results: Six
out of 12 cases of LMS showed strong and diffuse nuclear staining with p53 antibody
(50%). In contrast none of STUMPs and only one case of LBN cases showed focal
positive reaction with P53. Percentage of positive cells for ki67 in LMS was
14.92 while only 0.85% of cells in LBNs was labeled with Ki67 proliferative
marker. (P<0.001). Regarding steroid hormone receptors a significant loosing
trend was found in these receptors from benign toward malignant tumors through
LBN and STUMP cases.
Conclusion: Loss of inhibitory function of wild type P53 gene
in leiomyosarcoma is an essential event that discriminate frankly malignant
tumors from STUMP and atypical leiomyoma.