Uterine and Pelvic Conditions · Adenomyosis

A critical review of recent advances in the diagnosis, classification, and management of uterine adenomyosis

Tan J, Yong P, Bedaiwy MA

Published August 2019 Current opinion in obstetrics & gynecology
DOI 10.1097/gco.0000000000000555 PMID 31192829

Abstract

Purpose of Review

The purpose of this review is to summarize and highlight recent critical advances in the diagnosis, classification, and management of adenomyosis.

Recent Findings

Recent studies have clarified the specific mechanism through which adenomyotic lesions invade the underlying myometrium by epithelial-mesenchymal transition. Correlation studies using diagnostic MRI also strongly support the hypothesis of a different pathogenesis between the inner and outer myometrium forms of adenomyosis. Given advances in diagnostic imaging, several international organizations have also highlighted the importance of classification systems for adenomyosis. Finally, selective progesterone receptor modulators and gonadotropin-releasing hormone antagonists have demonstrated significant promise for treating pelvic pain and bleeding associated with adenomyosis, whereas novel fertility-preserving surgical techniques have been introduced to excise diffuse adenomyotic pathology while maintaining adequate uterine integrity.

Summary

Recent attempts at a uniform and reproducible classification system likely represent the first step for the development of a staging system for adenomyosis that can be correlated with the severity of clinical symptoms and promote an individualized therapeutic approach. Simultaneously, further insights into the etiology and pathogenesis as outlined in this review may also help in the development of targeted medical therapies.

Topics

By this author

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Uterine and Pelvic Conditions › Adenomyosis › Adenomyosis Diagnosis · Diagnostics › Tubal and Uterine Imaging › Sonohysterography · Clinical Guidelines and Standards › Diagnostic Criteria and Classification › Staging and Classification Systems
Justin Tan, Mohamed A Bedaiwy
J Tan, M Bedaiwy
PMID 31192829 31192829 DOI 10.1097/gco.0000000000000555 10.1097/gco.0000000000000555 Tan et al. 2019, Tan 2019