Immunohistochemical Study of Estrogen and Progesterone Receptors and the Proliferation Marker Ki-67 in Abdominal Wall Endometriosis

Medeiros, Francisco das Chagas and Filho, Manoel Oliveira and Junior, José Eleutério and Medeiros, Angelina da Silva (2021) Immunohistochemical Study of Estrogen and Progesterone Receptors and the Proliferation Marker Ki-67 in Abdominal Wall Endometriosis. International Journal of Research and Reports in Gynaecology, 4 (1). pp. 10-14.

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Abstract

Introduction: The scar from pelvic surgery in the abdominal wall can be a site of endometriotic implants in 0.03 to 1% of patients. This study aims to evaluate the immunohistochemical expression of the estrogen receptor (ER), progesterone receptor (PR), and cell proliferation marker Ki-67 in patients with abdominal wall endometriosis.

Materials and Methods: We investigated seven women with abdominal wall endometriosis who underwent surgery to remove a lesion at the Assis Chateaubriand Maternity, Fortaleza, Brazil. From tissue blocks, histological sections were subjected to immunohistochemistry to identify ER, PR, and Ki-67. For statistical significance, an unpaired t-test was applied with a 95% confidence interval.

Results: The mean patient age was 30.4 ± 1.13 years. ER expression in the epithelium and stroma had a mean score of 33.45 and 17.14, respectively, and the difference was not significant. PR had a mean epithelial score of 175.71 and a mean stromal score of 72.29, significantly different (p = 0.0339). Ki-67 had epithelial and stromal scores of 14.14 and 12.14, respectively, which were not significantly different.

Conclusions: Abdominal wall endometriosis presents ER and variable PR expression in the epithelium and stroma. The Ki-67 marker demonstrated a reduced proliferation index.

Item Type: Article
Subjects: Afro Asian Library > Medical Science
Depositing User: Unnamed user with email support@afroasianlibrary.com
Date Deposited: 21 Mar 2023 07:15
Last Modified: 30 Jul 2024 13:57
URI: http://classical.academiceprints.com/id/eprint/214

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