Endometrial Cancer Arising in Adenomyosis (EC-AIA): A Systematic Review

Author:

Raffone Antonio12ORCID,Raimondo Diego1ORCID,Maletta Manuela12,Travaglino Antonio3,Renzulli Federica12ORCID,Neola Daniele4,De Laurentiis Umberto12,De Laurentiis Francesco5,Mabrouk Mohamed6,Ianieri Manuel Maria7ORCID,Seracchioli Renato12,Casadio Paolo1,Mollo Antonio8

Affiliation:

1. Division of Gynaecology and Human Reproduction Physiopathology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy

2. Department of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy

3. Pathology Unit, Department of Woman and Child’s Health and Public Health, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy

4. Gynecology and Obstetrics Unit, Department of Neuroscience, Reproductive Sciences and Dentistry, School of Medicine, University of Naples Federico II, Naples, Italy

5. Obstetrics and Gynecology Unit, Salerno ASL, “Luigi Curto” Hospital, Polla, Salerno, Italy

6. Department of Obstetrics and Gynecology, Faculty of Medicine, University of Cambridge, Cambridge, UK

7. Division of Gynecologic Oncology, Department of Women’s and Children’s Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy

8. Gynecology and Obstetrics Unit, Department of Medicine, Surgery and Dentistry “Schola Medica Salernitana”, University of Salerno, 84081 Baronissi, Italy

Abstract

Endometrial cancer arising in adenomyosis (EC-AIA) is a rare uterine disease characterized by the malignant transformation of the ectopic endometrium within the adenomyotic foci. Clinicopathological and survival data are mostly limited to case reports and a few cohort studies. We aimed to assess the clinicopathological features and survival outcomes of women with EC-AIA through a systematic review of the literature. Six electronic databases were searched, from 2002 to 2022, for all peer-reviewed studies that reported EC-AIA cases. Thirty-seven EC-AIA patients from 27 case reports and four case series were included in our study. In our analysis, EC-AIA appeared as a rare disease that mainly occurs in menopausal women, shares symptoms with endometrial cancer, and is challenging to diagnose preoperatively. Differently from EC, it shows a higher prevalence of the non-endometrioid histotype, advanced FIGO stages, and p53-signature, which might be responsible for its worse prognosis. Future studies are necessary, to confirm our findings and further investigate this rare condition.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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