Could the Uterine Junctional Zone be Used to Identify Early-Stage Endometriosis in Women?

editorial OA: gold CC0 ⤵ 3 in-corpus citations
AI-generated summary by claude@2026-06, 2026-06-07

This paper examines the junctional zone's structural changes, particularly thickening and alterations, as potential non-invasive imaging indicators for identifying endometriosis and adenomyosis.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

Abstract

Although the correlation between endometriosis, junctional zone (JZ) hyperplasia and adenomyosis is still debated, the correlation among JZ and different etiological and clinical aspects is, today, well recognized. Starting from that, clinicians must consider in their own practice all the potential modifications of the JZ because the described could be correlated with reproductive or obstetrics disorders [1]. The accurate and analytical evaluation, case by case, of the JZ is one of the most crucial points in the flowchart of infertile patients and also endometriotic patients. An accurate evaluation of JZ and its potential modifications can provide important information for patients with endometriosis and/or infertility or chronic pelvic pain. We know that adenomyosis is a common gynecologic disease characterized by the migration of endometrial glands and stroma from the basal layer of endometrium into the myometrium, and could be associated with smooth muscle hyperplasia. The first author that mentioned adenomyosis and its histopathological features was Rokitansky in 1860 describing the invasion of stroma and endometrial glands inside the myometrium with different levels of invasion up to the serosa [2]. A common pathogenesis for adenomyosis and endometriosis has been hypothesized, and it is argued that endometrial stroma being in direct contact with the underlying myometrium allows communication and interaction, thus facilitating endometrial invagination or invasion of a structurally weakened myometrium during periods of regeneration, healing and re-epithelization. Dislocation of basal endometrium may also result in endometriosis through retrograde menstruation [3]. Pelvic endometriosis and uterine adenomyosis are variants of the same disease, which involves the dislocation of basal endometrium and results from a dysfunction and disease primarily at the level of the JZ [4]. Pelvic endometriosis, especially in its severe stages, is also strongly associated with JZ thickening [5–8]. Therefore, the evaluation of JZ and its alterations by non invasive imaging are very important, especially in patients with endometriosis. Adenomyosis is also defined as the chronic disruption of the boundary between the basal layer of the endometrium and the myometrium, known as the JZ, with the hallmark pathologic finding of endometrial glands and stroma within the myometrium [9]. Both parts of the JZ (endometrium and subendometrial myometrium) have a common embryological origin from the paramesonephric ducts and show cyclical changes during the menstrual cycle, whereas the outer myometrium is of nonparamesonephric mesenchymal origin [10]. The etiology of adenomyosis is not known, but there are recent interesting theories that consider adenomyosis as an expression of pathological endomyometrial JZ, trying to explain, in this Could the uterine junctional zone be used to identify early-stage endometriosis in women?

My notes (saved in your browser only)

Condition tags

mesh:D004715endometriosisadenomyosischronic_pelvic_paininfertility

MeSH descriptors

Endometriosis Endometriosis Uterus Uterus Adenomyosis Adenomyosis Adenomyosis Early Diagnosis Endometriosis Endometrium Endometrium Endometrium Female Humans Ultrasonography Uterus Women's Health

Citation neighborhood

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. [ expand to 2 hops ] — adds papers reached through this work's immediate citers/citees. Heavier; up to 60 extra dots.

References (20)

Cited by (3)

Source provenance

europepmc
last seen: 2026-06-04T01:30:01.192114+00:00
openalex
last seen: 2026-06-10T17:14:06.276822+00:00
pubmed
last seen: 2026-05-13T22:18:22.440000+00:00
License: CC0 · commercial use OK