Comparison of ER-α, ER-β, β-catenin, EGFR, CD117, p53, Ki-67 Expressions and Mitotic Rate between Superficial and Deep Fibromatoses
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Clinical Research
VOLUME: 26 ISSUE: 1
P: 46 - 52
2016

Comparison of ER-α, ER-β, β-catenin, EGFR, CD117, p53, Ki-67 Expressions and Mitotic Rate between Superficial and Deep Fibromatoses

Anatol J Gen Med Res 2016;26(1):46-52
1. Department Of Pathology, Afyonkarahisar Government Hospital, Afyonkarahisar, Turkey
2. Department Of Pathology, Tepecik Research And Training Hospital, Izmir, Turkey
3. Department Of Pathology, Hakkari Government Hospital, Hakkari, Turkey
No information available.
No information available
Received Date: 2015-12-01T20:30:40
Accepted Date: 2016-04-09T11:39:11
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Abstract

INTRODUCTION

Fibromatoses are divided into two groups as superficial fibromatoses and deep fibromatoses, which have different immunohistochemical profiles and clinical characteristics despite of their similar microscopic findings. Our aim was to evaluate the expressions of ER-α, ER-β, β-catenin, EGFR, CD117, p53, Ki-67 and mitotic rate in superficial and deep fibromatoses.

METHODS

Thirty-seven cases consisting of 15 superficial and 22 deep fibromatoses were reevaluated as regards ER-α, ER-β, β-catenin, EGFR, CD117, p53 expressions, Ki-67 proliferative index and the mitotic rate. Two groups were compared statistically and discussed.

RESULTS

ER-α expression was not observed in any case. ER-β and β-catenin expressions were more intense in the deep fibromatoses group. The ER-β intensity, β-catenin expression, Ki-67 proliferation index and mitotic rates were statistically significantly higher in the deep fibromatoses group (p=0.04, 0.01, 0.001, 0.001 respectively). There was no statistically significant difference in CD117, EGFR, and p53 expressions between the groups.

DISCUSSION AND CONCLUSION

ER-β intensity, β-catenin and Ki-67 expression rates and the mitotic index were statistically significantly higher in the deep fibromatoses group in our study. We suggest that these markers may have predictive value in determining the course of the lesions.

Keywords:
Fibromatoses, estrogen receptor beta, beta-catenin, Ki67 index, mitotic rate