Related Experiment Video
Updated: Jul 5, 2026

08:30
Immunophenotyping of Orthotopic Homograft (Syngeneic) of Murine Primary KPC Pancreatic Ductal Adenocarcinoma by Flow Cytometry
Published on: October 9, 2018
Mullerian adenosarcomas: an immunophenotypic analysis of 35 cases
Robert A Soslow1, Asya Ali, Esther Oliva
1Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA. soslowr@mskcc.org
The American Journal of Surgical Pathology
|May 13, 2008
Summary
Mullerian adenosarcomas (MAs) show a mesenchymal component resembling endometrial stromal tumors. Sarcomatous overgrowth in MAs is linked to decreased expression of ER, PR, and CD10, and increased proliferation.
Area of Science:
- Gynecologic Pathology
- Surgical Pathology
- Oncology
Background:
- Mullerian adenosarcomas (MAs) are rare neoplasms with benign epithelial and malignant mesenchymal components.
- The mesenchymal component dictates the clinical behavior and differential diagnosis of MAs.
- Understanding the immunophenotypic profile is crucial for accurate diagnosis and prognosis.
Purpose of the Study:
- To determine the immunophenotypic profile of the epithelial and mesenchymal components of MAs.
- To identify differences between conventional mesenchymal areas and sarcomatous overgrowth.
- To correlate immunophenotypic findings with tumor behavior.
Main Methods:
- Immunohistochemical analysis of 35 MAs (28 without sarcomatous overgrowth, 7 with sarcomatous overgrowth).
- Staining for ER, PR, AR, CD10, WT1, muscle markers, cytokeratin, CD34, calretinin, inhibin, c-kit, and Ki-67.
- Comparison of marker expression between conventional and sarcomatous areas.
Main Results:
- Mesenchymal components typically expressed ER, PR, WT1, and CD10, similar to endometrial stromal tumors.
- Sarcomatous overgrowth areas showed reduced expression of ER, PR, and CD10 compared to conventional areas.
- Ki-67 proliferation index was significantly higher in sarcomatous overgrowth areas (median 28%) than in conventional areas (median 5%).
- Epithelial components expressed ER, PR, and cytokeratin.
Conclusions:
- The immunophenotype of most MAs resembles endometrial stromal tumors.
- Loss of ER, PR, and CD10 expression in sarcomatous overgrowth areas suggests dedifferentiation.
- Increased proliferation in sarcomatous areas correlates with aggressive behavior.