A study of PTEN expression in endometrial hyperplasia and endometrioid type of endometrial carcinoma

  • Dr. M. Shanmugapriya Department of Pathology, Meenakshi Medical College and Research Institute, Kanchipuram, Tamil Nadu, India.
  • Dr. M. Sudha Department of Pathology, Melmaruvathur Adhiparasakthi Institute of Medical Sciences Research Institute, Melmaruvathur, Tamil Nadu, India
  • Dr. Geetha Prakash Department of Pathology, Meenakshi Medical College and Research Institute, Kanchipuram, Tamil Nadu, India
Keywords: Phosphatase and tensin homologue (PTEN), Endometrial hyperplasia (EH), Complex atypical hyperplasia (CAH), Endometrioid endometrial carcinoma (EEC)

Abstract

Background: To analyze the role of PTEN expression in hyperplastic and neoplastic endometrium by immunohistochemistry and to find the grades of PTEN expression in neoplastic, hyperplasic and normal endometrium.

Methods: 100 numbers of endometrial samples were studied retrospectively. The tissue were fixed in formalin and taken up for routine histopathological and immunohistochemistry studies.

Results: In our study PTEN is well expressed in a score of 2+ and 1+ in cyclical endometrium and hyperplasia without atypia whereas altered PTEN expression was noted in atypical hyperplasias and endometroid type of endometrial carcinoma in a score of 0and 1+.

Conclusion: The current study proved that PTEN expression is down regulated in endometrial pathological condition. Immunohistochemical evaluation of PTEN expression was useful in screening precancerous hyperplasia lesions and detecting earliest stage of endometrial carcinogenesis.

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A study of PTEN expression in endometrial hyperplasia and endometrioid type of endometrial carcinoma
CITATION
DOI: 10.17511/jopm.2017.i01.07
Published: 2017-03-31
How to Cite
Dr. M. Shanmugapriya, Dr. M. Sudha, & Dr. Geetha Prakash. (2017). A study of PTEN expression in endometrial hyperplasia and endometrioid type of endometrial carcinoma. Tropical Journal of Pathology and Microbiology, 3(1), 39-45. https://doi.org/10.17511/jopm.2017.i01.07
Section
Original Article