Obstetrics, Gynaecology and Reproductive Medicine
Volume 20, Issue 4 , Pages 116-120, April 2010

Endometrial hyperplasia: a clinician's review

Michael M Hannemann MBBCh PhD MRCOG is a Consultant Gynaecological Oncologist at the Royal Devon and Exeter NHS Foundation Trust, Exeter, UK

Helen M Alexander MA BChir FRCPath is a Specialist Registrar in Histopathology at the Royal Devon and Exeter NHS Foundation Trust, Exeter, UK

Nichola J Cope MA MBChB FRCPath is a Consultant Histopathologist at the Royal Devon and Exeter NHS Foundation Trust, Exeter, UK

Nigel Acheson MBChB MD FRCOG is a Consultant Gynaecological Oncologist at the Royal Devon and Exeter NHS Foundation Trust, Exeter, UK

Andrew Phillips MBChB MA is a Speciality Trainee in Obstetrics and Gynaecology at the Royal Devon and Exeter NHS Foundation Trust, Exeter, UK

Abstract 

Endometrial hyperplasia is considered present when the ratio of glandular to stromal tissue of the endometrium is greater than 1:1. Further differentiation is made into simple or complex hyperplasia with or without the presence of cytological atypia. Such changes are caused by excess or unopposed oestrogenic stimulation. Clinically endometrial hyperplasia is often asymptomatic but can present as abnormal uterine bleeding. Many cases are detected incidentally or following abnormal vaginal bleeding by an increase in the normal endometrial thickness on transvaginal ultrasonography (TVS). An endometrial biopsy can be obtained using a pipelle or at hysteroscopy, and examination of this allows a histological diagnosis. Cytological atypia mandates active intervention as its presence correlates with both a significant risk of progression to endometrial cancer as well as an increased rate of occult endometrial cancer. Hysterectomy is therefore the treatment of choice. The absence of cytological atypia confers a lower risk of malignant change. Thus management is more conservative. Progestogens are used to oppose the oestrogenic stimuli, coupled with ongoing surveillance.

Keywords: endometrial cancer, endometrial hyperplasia, oestrogen, post-menopausal bleeding

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PII: S1751-7214(10)00003-5

doi:10.1016/j.ogrm.2010.01.002

Obstetrics, Gynaecology and Reproductive Medicine
Volume 20, Issue 4 , Pages 116-120, April 2010