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Trial Title: the Value of Immunohistochemical Expression of Moesin in Endometrial Hyperplasia and Endometrial Carcinoma

NCT ID: NCT05619159

Condition: Endometrial Cancer and Endometrial Hyperplasia

Conditions: Official terms:
Endometrial Neoplasms
Endometrial Hyperplasia
Hyperplasia

Study type: Observational

Overall status: Unknown status

Study design:

Time perspective: Retrospective

Intervention:

Intervention type: Device
Intervention name: microscopic pathological evaluation
Description: description of moesin expression between endometrial hyperplasia and endometrial carcinoma
Arm group label: endometrial carcinoma smples
Arm group label: endometrial hyperplasia samples

Summary: Endometrial carcinoma (EC) is the most prevalent invasive carcinoma of the female genital tract in developed countries, while it ranks as the second most frequently occurring neoplasm of women in developing countries, after carcinoma of the cervix uteri. The vast majority of ECs occur in perimenopausal and postmenopausal women . ECs are classified into two distinct phenotypes; type I which represents more than 80% of all cases of ECs, it has a favorable prognosis. This type is linked to excess, unopposed hyper-estrogenic condition and it is almost always preceded by endometrial hyperplasia. On the contrary, type II endometrial carcinoma is less common than type I, representing less than 10% of all cases of ECs. Type II endometrial carcinomas are high grade, poorly differentiated and estrogen-independent tumors .

Criteria for eligibility:

Study pop:
females presented to gynecology department in sohag university hospital and sohag oncology center

Sampling method: Probability Sample
Criteria:
Inclusion Criteria: - Hysterectomy specimens diagnosed as endometrial hyperplasia and endometrial adenocarcinoma. - All cases of endometrial biopsies obtained by curettage (D&C) diagnosed as endometrial hyperplasia. - Cases of cyclical endometrium obtained from endometrial curettage or hysterectomy specimens done for pathological conditions other than hyperplastic or neoplastic endometrial lesions. - Complete clinical data. Exclusion Criteria: - Patients with a history of preoperative chemotherapy and /or radiotherapy. - Biopsies with predominantly blood clots. - Insufficient or tiny tissue biopsies.

Gender: Female

Gender based: Yes

Minimum age: N/A

Maximum age: N/A

Locations:

Facility:
Name: Sohag University Hospital

Address:
City: Sohag
Country: Egypt

Contact:
Last name: Magdy M Amin, professor

Start date: November 2022

Completion date: May 2023

Lead sponsor:
Agency: Sohag University
Agency class: Other

Source: Sohag University

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05619159

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