Introduction
Abnormal uterine bleeding (AUB) is a comprehensive term
that encompasses nongestational abnormal bleeding from
the uterus in women of reproductive age. AUB is character-
ized by irregularities in the duration, volume, frequency,
and/or regularity of uterine bleeding. Additionally, it
includes postmenopausal bleeding, de fined as any bleeding
occurring after menopause in women who are not receiving
hormonal therapy, as well as unscheduled or excessive
bleeding in those undergoing hormonal therapy.
1
Research indicates that approximately one-third of wom-
en will experience symptoms associated with AUB at some
stage in their lives. This condition is most frequently ob-
served in women during menarche and the perimenopausal
phase.2 Notably, up to 50% of affected women do not pursue
medical evaluation.
In 2007, the International Federation of Gynecology and
Obstetrics (FIGO) Menstrual Disorders Working Group estab-
lished standardized terminology and de finitions for various
types of AUB (referred to as AUB system 1). The subsequent
classification of the causes of AUB was undertaken in 2011
using the PALM-COEIN classi fication system (designated as
AUB system 2).
1,3 This initiative replaced previously
employed, poorly de fined, and often confusing terms such
as menorrhagia, metrorrhagia, and dysfunctional uterine
Keywords
► abnormal uterine
bleeding
► PALM COEIN
classification
► structural and
nonstructural causes
of abnormal uterine
bleeding
Abstract
Abnormal uterine bleeding (AUB) is a commo n gynecological symptom experienced by
approximately one-third of women at some point in their lives. There are various
terminologies used to describe the symptoms of AUB, which can lead to inconsistency
in interpretation. To address this, the International Federation of Gynecology and
Obstetrics (FIGO) Menstrual Disorders Working Group established standardized termi-
nology and de finitions for different types of AUB in 2007. AUB can have both structural
and nonstructural causes, and it is possible for more than one cause to coexist in a
single patient. To categorize and evaluate the causes of AUB consistently, FIGO de fined
ac l a s s ification system in 2011 known as the AUB system 2. This system is referred to by
the acronym PALM-COEIN. “PALM” stands for the structural causes: Polyp (P),
Adenomyosis (A), Leiomyoma (L), and Malignancy and hyperplasia (M). “COEIN”
represents the nonstructural causes: Coagulopathy (C), Ovulatory dysfunction (O),
Endometrial causes (E), Iatrogenic factors (I), and causes that are Not yet classi fied (N).
In this article, we review the standardized de finitions and terminologies used to
d e s c r i b et h es y m p t o m so fA U Ba n dd i s c u s st h er o l eo fi m a g i n ga n da p p r o a c hi n
identifying and classifying its causes.
article published online
January 15, 2026
DOI https://doi.org/
10.1055/s-0045-1815710.
ISSN 2581-9933.
© 2026. The Author(s).
This is an open access article published by Thieme under the terms of the
Creative Commons Attribution License, permitting unrestricted use,
distribution, and reproduction so long as the original work is properly cited.
(https://creativecommons.org/licenses/by/4.0/)
Thieme Medical and Scienti fic Publishers Pvt. Ltd., A-12, 2nd Floor,
Sector 2, Noida-201301 UP , India
Review Article
THIEME
54
Article published online: 2026-01-15
bleeding. An update to these classi fication systems was
published in 2018.
Moreover, FIGO published recommended terminologies
and de finitions concerning myometrial abnormalities in
2015, followed by updates in 2021 through the Morphologi-
cal Uterus Sonographic Assessment (MUSA) classi fication
system.4,5 Furthermore, the FIGO ovulatory disorders classi-
fication system was introduced in 2022. 6 This review aims to
elucidate the causes of AUB, their associated imaging fea-
tures, and the differential diagnoses relevant to this
condition.
Definition and Terminologies
(AUB System 1)
A normal menstrual cycle is characterized by a frequency
ranging from 24 to 38 days, 4.5 to 8 days, and a blood flow
measuring between 5 and 80 mL. Additionally, the cycle
length may vary by 2 to 20 days over 12 months. Deviations
from these established parameters are classi fied as AUB. 1
►Table 1 delineates the accepted de finitions and termi-
nology about various types of AUB, while ►Table 2 provides a
comprehensive overview of the acceptable abbreviations and
their corresponding de finitions.
AUB can be categorized into two types: acute and chronic.
Acute AUB is de fined as a sudden episode of bleeding in a
nonpregnant woman that requ ires immediate medical in-
tervention to avert further blood loss. In contrast, chronic
AUB is characterized by abnormal bleeding from the uterine
corpus that deviates from normal duration, volume, or
frequency for the majority of the preceding 6 months.
AUB System 2
The AUB system 1 addresses the inconsistencies in terminol-
ogy utilized to describe AUB. Nevertheless, discrepancies
remain in the investigation and categorization of the causes
of AUB, with several of these causes potentially coexisting in
a single individual. In response to this issue, the FIGO has
introduced the PALM-COEIN classi fication system.
PALM-COEIN is an acronym that categorizes the etiologies
of AUB into two primary groups: structural and nonstruc -
tural. The “PALM” category encompasses structural causes
that can be identi fied through imaging or histopathological
examination: Polyp (P), Adenomyosis (A), Leiomyoma (L),
and Malignancy and hyperplasia (M). The “COEIN” category
comprises nonstructural causes, which include Coagulop-
athy (C), Ovulatory dysfunction (O), Endometrial causes (E),
Table 1 Summary of terminologies and de fin i t i o n so fv a r i o u st y p e so fA U B
Parameters of the menstrual cycle and menstruation Descriptive terms Definitions
Frequency of cycle (d) Frequent 38
Regularity of cycles - Variation over 12 months Absent/amenorrhea No bleeding in 90 days
Regular Variation: /C62 to 20 days
Irregular Variation > 20 days
Duration of flow (d) Prolonged > 8
Normal 4.5 –8
Shortened 80
Normal 5 –80
Light < 5
Abbreviation: AUB, abnormal uterine bleeding.
Table 2 Acceptable abbreviations describing menstrual symptoms
Abbreviation Expansion Definition
AUB Abnormal uterine bleeding Any deviation in menstrual flow/cycle
HMB Heavy menstrual bleeding Excessive menstrual blood loss that interferes with the physical,
emotional, social, and material quality of life
HPMB Heavy, prolonged menstrual
bleeding
E x c e s s i v eb l o o dl o s sa l o n gw i t hp r o l o n g e db l e e d i n gf o r> 8 days
IMP Intermenstrual bleeding Irregular episodes of bleeding occurring between otherwise normal
menstrual cycles
PMB Postmenopausal bleeding Bleeding occurring > 1 year after the acknowledged menopause
Journal of Gastrointestinal and Abdominal Radi ology ISGAR Vol. 9 No. 1/2026 © 2026. The Author(s).
Imaging in Abnormal Uterine Bleeding Renganathan et al. 55
Iatrogenic factors (I), and causes that are Not yet classi fied
(N).
This classi fication system has been developed with con-
tributions from clinicians and researchers across 6 conti-
nents and over 17 countries. It facilitates a systematic
approach to diagnosis, thereby enhancing clinical communi-
cation, research methodologies, and treatment strategies for
AUB.
Endometrial Polyp: AUB-P
Endometrial polyps form when endometrial glands and
stroma excessively grow within the endometrium. Endome-
trial polyps are primarily composed of epithelial tissue on
the surface and have a predominantly vascular core. These
polyps can be classified into three categories: sessile, pedun-
culated, or prolapsing. A prolapsed polyp may exhibit areas
of squamous metaplasia, infection, or ulceration.
7
These polyps can range from a few millimeters to several
centimeters in diameter and may appear as single or multiple
growths. Endometrial polyps can occur at any age but are
most found between the ages of 40 and 49. Patients with
endometrial polyps may either be asymptomatic or present
with AUB, which is the most common symptom. The preva-
lence of endometrial polyps in reproductive-aged women
experiencing AUB is estimated to be between 20 and 40%.
8
The most common patterns include menorrhagia and inter-
menstrual bleeding (IMB). The other symptoms are abdomi-
nal or pelvic pain and infertility. The location of the polyp,
number, and diameter do not correlate with the reported
symptoms.
9
Chronic use of tamoxifen has been linked to the develop-
ment of endometrial polyps, with an incidence rate ranging
from 20 to 35%.
10 Additionally, hormone replacement thera-
py for menopausal symptoms may also contribute to the
formation of endometrial polyps. Symptoms can include
irregular bleeding and a thickened endometrium on ultra-
sound (US). 11
While most polyps are typically benign, there is a small
risk of them becoming malignant. 12 Malignant changes in
endometrial polyps are associated with the patient ’s age,
particularly in those over 60, and their menopausal status,
especially in postmenopausal women. The other risk factors
for malignant endometrial polyps include the size of the
polyps, the presence of symptomatic bleeding, and polycys-
tic ovary syndrome (PCOS).
13 The prevalence of malignant
endometrial polyps is 4.47% in symptomatic postmenopaus-
al females, compared to 1.51% in asymptomatic postmeno-
pausal females.
14
Imaging
Transvaginal US (TVS) represents the most utilized and
effective technique for imaging pelvic structures. The find-
ings from US examinations may occasionally be nonspeci fic,
revealing either diffuse or localized echogenic thickening of
the endometrium. 15 In patients presenting with postmeno-
pausal bleeding, an endometrial thickness exceeding 4 mm is
associated with the potential for endometrial pathology,
including the presence of polyps. 11
Saline infusion sonography (SIS) is a better method for
evaluating the lesions within the endometrial cavity. It
involves instilling about 5 to 30 mL of warmed saline into
the cavity using a thin catheter during the proliferative phase
of the menstrual cycle.
Endometrial polyps are more effectively visualized utiliz-
ing SIS, as the introduced fluid delineates the polyps dis-
tinctly. Moreover, SIS enhances the differentiation between
submucosal fibroids and endometrial polyps by distinctly
illustrating their respective positions within the endometrial
layer. Specifically, endometrial polyps are observed to arise
from the endometrial layer, whereas submucosal fibroids are
positioned beneath this layer.
16
The contraindications for SIS include the presence of
active uterine or cervical infections, as well as pregnancy.
Furthermore, SIS provides a superior evaluation of the
adnexa and cornua in comparison to TVS.
During the TVS/SIS procedure, the following details are
noted when the polyp is detected: the number and type of
the polyp, its site of attachment within the endometrial
cavity, and the presence and pattern of internal vascularity.
Submucosal polypoidal adenomyoma can resemble an
endometrial polyp; however, it often contains cysts of vary-
ing sizes. These cysts, along with the stroma, may exhibit
areas of focal hemorrhage, resulting in dark brown material
filling the cystic spaces. On imaging, submucosal polypoidal
adenomyoma typically shows cysts accompanied by myo-
metrial invasion.
17
In contrast, endometrial polyps usually have a smooth,
bosselated surface and tend to appear fibrous when viewed
in cross-section. They often possess small cystic spaces that
reflect the dilation of glandular elements, but they do not
exhibit myometrial invasion ( ►Figs. 1 and 2).18
While endometrial carcinoma can also show myometrial
invasion, it rarely contains cysts. Therefore, when both cysts
and myometrial invasion are observed, submucosal poly-
poidal adenomyoma should be considered. Magnetic reso-
nance imaging (MRI) can help differentiate between these
three entities.
18,19
Imaging thus plays a vital role in predicting the malignant
potential of a polyp thereby guiding further management.
Adenomyosis (AUB-A)
Adenomyosis is a benign gynecological condition that pri-
marily affects multiparous women between the ages of 30
and 50. While many individuals with this condition remain
asymptomatic, it may present with symptoms such as AUB,
dysmenorrhea, chronic pelvic pain, and dyspareunia.
10
The prevalence of adenomyosis exhibits considerable
variation, ranging from 5 to 70%, depending on the diagnostic
Methods
employed, with an average prevalence estimated at
20 to 30%. 20 The precise etiology of adenomyosis remains
unclear; however, potential risk factors include hyperestro-
genism and a history of surgeries, such as cesarean sections
and dilatation and curettage. The hallmark of adenomyosis is
the presence of ectopic endometrial glands and stroma
within the myometrium, accompanied by hypertrophy and
hyperplasia of the smooth muscle.
21
Journal of Gastrointestinal and Abdominal Radio logy ISGAR Vol. 9 No. 1/2026 © 2026. The Author(s).
Imaging in Abnormal Uterine Bleeding Renganathan et al.56
Imaging
Diagnosis of adenomyosis typically involves various imaging
modalities, including TVS and MRI. TVS is generally the initial
imaging technique utilized for evaluating patients present-
ing with AUB. The MUSA group has established a consensus
on the terminology to be used when documenting US find-
ings related to myometrial lesions. The US report should
encompass the following features: the presence or absence of
adenomyosis, its anatomical location, classi fication as focal
or diffuse, cystic versus noncystic nature, involvement of
uterine layers, and the extent and dimensions of the lesion.
The findings of adenomyosis can be categorized into
direct and indirect features.
5 Direct features, observable
through US imaging, are characteristic of adenomyosis,
whereas indirect features result from the presence of ectopic
endometrium within the myometrium ( ►Fig. 3 ).
The direct US features indicative of adenomyosis include:
Myometrial cysts
Hyperechoic islands
Echogenic subendometrial lines and buds
The indirect features may present as:
A globular uterine shape
Asymmetric thickening of the myometrium
Fan-shaped shadowing
Translesional vascularity
An irregular and interrupted junctional zone (JZ)
It is crucial to note that in the absence of direct features,
the presence of indirect features alone does not provide
conclusive evidence for the diagnosis of adenomyosis. Fur-
thermore, a regular and uninterrupted JZ is a reliable indica-
tor of the absence of this condition.
22 ►Table 3 shows the
classification and reporting guidelines for adenomyosis.
MRI, due to its superior soft tissue resolution, facilitates
the differentiation between adenomyosis and leiomyomas,
as well as other uterine pathologies. The sequences most
commonly employed include T2-weighted imaging in axial,
coronal, and sagittal planes, along with T1-weighted imaging
in axial and sagittal planes. It is pertinent to note that the use
of contrast MRI does not yield any additional diagnostic
information for adenomyosis.
Recently, a classification system for MRI findings has been
proposed by Kobayashi and Matsubara,
23 which encom-
passes five distinct parameters:
1. Affected area: This parameter differentiates between
internal myometrium (internal adenomyosis, which
involves the inner one-third of the uterine wall) and
external myometrium (external adenomyosis).
2. Pattern: Adenomyosis is categorized as either diffuse or
focal.
Fig. 1 Transvaginal ultrasound ( A) and sonohysterosalpingography ( B) images demonstrate a solitary, homogeneously hyperechoic intra-
cavitary lesion with smooth outline arising from the posterior wall with preserved endom yometrial junction(marked by white arrows in A and B).
Sonohysterosalpingography image of another patient ( C) shows similar lesion demonstrating single vessel with no branching (marked by black
arrow in C). These findings are consistent with endometrial polyp (abnormal uterine bleeding [AUB]-P).
Fig. 2 Transvaginal ultrasound ( A) and Doppler ( B) images demonstrate a solitary hyperechoic intracavitary lesion with regular cysts, color score of 2
and preserved endomyometrial junction (marked by black arrow in A). T2 axial ( C) and postcontrast sagittal T1 fat-saturated ( D) magnetic resonance
imaging (MRI) images show a well-de fined polypoidal lesion limited to the endometrial cavity with regular nonenhancing cystic areas within with
maintained subendometrial enhancement (marked by white arrow in C and black arrow in D) (abnormal uterine bleeding [AUB]-P).
Journal of Gastrointestinal and Abdominal Radi ology ISGAR Vol. 9 No. 1/2026 © 2026. The Author(s).
Imaging in Abnormal Uterine Bleeding Renganathan et al. 57
3. Size: This is classi fied into three volumetric categories:
less than one-third, less than two-thirds, or more than
two-thirds of the uterine wall.
4. Location: The location is speci fied as anterior, posterior,
left-lateral, right-lateral, or fundal.
5. Presence of concomitant pathologies: This includes the
absence of additional conditions, peritoneal endo-
metriosis, ovarian endometrioma, deep in filtrating
endometriosis (DIE), uterine fibroids, or other relevant
pathologies.
Internal adenomyosis is further subdivided into three
types: focal, diffuse, and super ficial. The focal and diffuse
types are associated with JZ hypertrophy, whereas the
superficial type is not associated with JZ hypertrophy. Exter-
nal adenomyosis involves the outer myometrium, extending
Fig. 3 (A and E) Transvaginal ultrasound image of a patient with pain during menstruation showing globular enlargement of the uterus with
heterogeneous myometrial echoes, indistinct endomyometrial junction (black dotted line in A) with tiny myometrial cysts (black arrows in
A and E), and hyperechogenic islands (white arrows in A and E), consistent with diffuse adenomyosis. Volume contrast image (VCI) in E better
depicts the findings. ( B) Transabdominal ultrasound image shows asymmetrical thickening of anterior myometrium (marked by white dotted
lines in B) with heterogeneous myometrial echoes and hyperechogenic islands consistent with anterior wall adenomyosis. ( C and D) Transvaginal
ultrasound and Doppler images show an ill-de fined heterogeneous focal lesion with thin lines of posterior shadowing (marked by white stars in
(C)a n d( D) and diffuse vascularity consistent with adenomyoma (abnormal uterine bleeding [AUB]-A).
Table 3 Classification and reporting guideline for ultrasound features of adenomyosis
Criteria Ultrasound features
Presence or absence of adenomyosis Look for the direct and indirect features using the MUSA criteria
Location Anterior, posterior, right lateral, left lateral, and fundal
Differentiation Focal if > 25% of the circumference of the lesion is surrounded by normal
myometrium
Diffuse if < 25% of the lesion is surrounded by normal myometrium
Mixed type if both focal and diffuse adenomyosis coexist
Presence or absence of cysts Cystic - presence of cysts, which are anechoic or low-level echoes and surrounded by
an echogenic rim
Noncystic adenomyosis - absence of cysts
Uterine layer involvement Involvement of junctional zone (inner myometrium, Type 1), middle myometrium
(Type 2), or outer myometrium (Type 3)
Extent Mild ( 50% affected).
Size of lesion Measured and documented in the plane of the largest diameter of the largest lesion.
If more than 1 adenomyotic lesion is present in different locations, the sum of
volumes of different lesions should be taken into account to assess the total extent
Abbreviation: MUSA, Morphological Uterus Sonographic Assessment.
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Imaging in Abnormal Uterine Bleeding Renganathan et al.58
to the serosa, while sparing the JZ. This form of adenomyosis
is frequently observed in young nulliparous women and is
often associated with deep pelvic endometriosis (DIE), mak-
ing it distinguishable from endometriotic deposits when DIE
coexists.
On MRI, the characteristic features of both internal and
external adenomyosis manifest as ill-de fined areas of T2-
weighted hypointensity, attributed to smooth muscle prolif-
eration, alongside multiple T2-weighted hyperintense foci.
Small cystic regions may also be present. In T1-weighted
imaging, small areas of T1 hyperintensity may be observed
within the adenomyotic regions, indicating the presence of
hemorrhage.
►Fig. 4 shows the MRI features of adenomyosis.
Adenomyomas typically present as well-de fined, heteroge-
neous lesions con fined within the myometrium, without
involving the JZ or the serosa. 24
Leiomyoma
Benign fibromuscular tumors of the myometrium are often
referred to by various terms, including “fibroid,”“ leio-
myoma,” and “myoma.” According to the FIGO, the term
“leiomyoma” is regarded as the most precise designation.
Leiomyomas represent the most common benign tumors of
the uterus and are frequently asymptomatic. However, they
may contribute to AUB, particularly when located in a
submucosal position.
25
Imaging
Diagnosis of leiomyomas typically occurs through the iden-
tification of an enlarged uterus or pelvic mass during clinical
examination. The initial and preferred method of investiga-
tion for diagnosing leiomyomas is US, which may be con-
ducted via transabdominal and/or transvaginal approaches.
TVS is recognized for its increased sensitivity in detecting
small leiomyomas or submucosal leiomyomas, especially in
patients with obesity.
26 Literature suggests that the sensi-
tivity and speci ficity of US in the identi fication of fibroids
exhibit considerable variability, ranging from 24 to 96% for
sensitivity and from 29 to 93% for speci ficity. SIS has been
shown to provide signi ficantly higher sensitivity (85 –91%)
and specificity (83–100%) in detecting abnormalities such as
polyps, submucosal fibroids, and adhesions. 26
MRI is noted for its superior sensitivity (88 –93%) and
specificity (66–91%) in detecting fibroids and differentiating
them from focal adenomyosis. 26 Furthermore, MRI findings
are reproducible and capable of accurately de fining the
extent of fibroid degeneration.
US
On US, leiomyomas present as well-de fined solid masses
characterized by a whorled appearance, posterior shadow-
ing, and circumferential vascularity. The MUSA consensus
opinion describes the classical imaging features of fibroids
and points to differentiate them from adenomyosis. 4
The US report should encompass the total uterine volume,
the number of leiomyomas, the volumes of up to four
leiomyomas, and their speci fic locations as per the FIGO
classification. This classi fication delineates the relationships
of the fibroids with the endometrium and serosa, as well as
the uterine wall (anterior, posterior, right or left lateral wall,
or fundal region) and their vertical positioning (upper or
lower uterine segment). The anatomical location of fibroids
is a critical parameter in predicting bleeding symptoms, with
submucosal fibroids demonstrating a greater association
with an increased risk of bleeding than their size.
The FIGO PALM-COIEN classi fication system for
leiomyomas comprises primary, secondary, and tertiary
categorizations. The primary classi fication addresses the
presence or absence of leiomyomas, irrespective of their
number, size, or location. The secondary classi fication differ-
entiates fibroids based on the presence or absence of sub-
mucosal components, categorizing them as submucosal (SM)
or other (O) leiomyomas. Furthermore, the tertiary classi fi-
cation introduces additional categorizations for submucosal,
Fig. 4 T2 sagittal magnetic resonance imaging (MRI) image ( A) globular enlargement of the uterus with diffuse thickening of junctional zone
with multiple myometrial cysts (marked by white arrows in A) consistent with diffuse adenomyosis. T2 oblique axial MRI image ( B) of the uterus
shows an ill-de fined T2 hypointense area with multiple tiny T2 hyperintense cysts within the posterior myometrium extending from the
junctional zone (marked by white star in B) consistent with focal adenomyosis. T2 sagittal MRI image ( C) shows diffuse thickening of the
junctional zone with subendometrial T2 hyperintense lines (marked by black arrow in C) involving the anterior wall consistent with adenomyosis
(abnormal uterine bleeding [AUB]-A).
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Imaging in Abnormal Uterine Bleeding Renganathan et al. 59
intramural, subserosal, and transmural locations. 27 ►Fig. 5
shows the US features of intramural, subserosal, and submu-
cosal fibroids.
Applying the FIGO classi fication in the imaging assess-
ment of leiomyomas enhances the correlation between
clinical symptoms and imaging features, thereby improving
confidence in identifying the underlying etiology. The
FIGO classi fication further helps in determining the appro-
priate management for each subtype, guiding the choice
between minimally invasive and surgical techniques.
►Table 4 presents the FIGO classi fication of fibroids
according to their location. ►Fig. 6 shows the various FIGO
classes of fibroids.
MRI
MRI is indicated in cases where US findings are indetermi-
nate or before the planning of uterus-sparing interventions
such as myomectomy or uterine artery embolization, as it
provides accurate information regarding vascularity and the
extent of degeneration. Furthermore, MRI is the imaging
modality of choice for follow-up assessments following
uterus-sparing treatments.
28
Table 4 FIGO secondary and tertiary system of classi fication of leiomyomas
Secondary system Tertiary system:
FIGO class
Definition
SM - Submucous 0 Pedunculated intracavitary with stalk diameter /C2010% of the mean diameter
of leiomyoma
1 Submucosal with < 50% intramural component
2 Submucosal with /C2150% intramural component
3 Contacts endometrium, 100% intramural
0-O t h e r 4 I n t r a m u r a l
5S u b s e r o s a l w i t h /C2150% intramural
6S u b s e r o s a l w i t h < 50% intramural
7 Pedunculated subserosal with stalk diameter /C2010% of the mean diameter of
the leiomyoma
8 Other (e.g., cervical/ parasitic, etc.)
Hybrid - Contacts both
the endometrium
and serosa
Two numbers
separated by
ah y p h e n
E.g., 2 –5
First number - relationship with the endometrium
Second number - relationship with serosa
2–5: Submucosal and subserosal, each with < 50% submucosal and
subserosal components, respectively
Abbreviation: FIGO, International Federation of Gynecology and Obstetrics.
Fig. 5 Transvaginal ultrasound image ( A) shows a well-circumscribed hypoechoic lesion within the myometrium —intramural International
Federation of Gynecology and Obstetrics (FIGO) class 4 fibroid (white arrow) and similar lesion adjacent to serosa with < 50% myometrial
component —FIGO class 6 subserosal fibroid(black arrow) (abnormal uterine bleeding [AUB]-L O). Transvaginal ultrasound image ( B)s h o w saw e l l -
defined hypoechoic lesion in the anterior wall extending to the endometrial cavity with < 50% intramural component and disruption of
endomyometrial junction (marked by white arrow) —FIGO class 1 submucosal fibroid (AUB-L SM).
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Imaging in Abnormal Uterine Bleeding Renganathan et al.60
In MRI examinations, typical leiomyomas exhibit hypo-
intensity on T2-weighted images, isointensity on T1-weight-
ed images, and demonstrate no diffusion restriction along
with heterogeneous postcontrast enhancement. In instances
of degeneration, fibroids may present with heterogeneous
signals or increased signal intensity on T2-weighted images,
accompanied by minimal or absent enhancement. Cellular
leiomyomas are characterized by intermediate signal
intensity on T2-weighted images, evidence of diffusion
restriction, and pronounced enhancement after contrast
administration.
In older women, the identi fication of recent or rapidly
enlarging lesions, heterogeneous signal intensity with hem-
orrhagic or necrotic areas, diffusion restriction within the
lesion, and signs of invasion into adjacent tissues should raise
clinical suspicion for leiomyosarcoma.
29
Endometrial Malignancy/Hyperplasia (AUB-M)
Endometrial hyperplasia is the abnormal proliferation of
endometrial stroma and glands, which is representative
of an entire spectrum of endometrial variation, ranging
from mild atypical glandular proliferation to obvious
neoplasia.
30
Hyperplasia and neoplasms form an important compo-
nent of the long list of etiologies of AUB, especially in women
in the reproductive age group.
30 The primary purpose of the
PALM-COEIN system is to categorize the etiologies of AUB,
and on further identi fication of speci fic etiologies, such as
endometrial hyperplasia, classi fication according to the
World Health Organization (WHO) classi fication systems
must be performed. 3
The classi fication of endometrial hyperplasia according
to the revised WHO classi fication system, 2014, 3 is as
follows:
(1) Hyperplasia without atypia
(2) Atypical hyperplasia/endometrioid intraepithelial neop-
lasia
Hyperplasia without atypia is a form of benign prolifera-
tion that spontaneously regresses once the internal hormon-
al stimulus is corrected. Only about 1 to 3% of the times do
these progress to invasive disease when there is uncontrolled
prolonged exposure to the hormonal stimulus. On the other
hand, atypical endometrial hyperplasias exhibit mutations
within them that are characteristic of invasive malignancies.
Understandably, close to 60% of these harbor concurrent
Fig. 6 (A) T2 axial magnetic resonance (MR) image shows multiple well-de fined predominantly T2 hypointense lesions (marked by white stars in
A) in submucosal location with > 50% intramural component —International Federation of Gynecology and Obstetrics (FIGO) class 2 submucosal
fibroids. ( B) T2 sagittal MR image shows a well-encapsulated T2 hypointense lesion within the posterior myometrium (marked by white star in B)
—FIGO class 4 intramural fibroid. ( C) T2 sagittal MR image shows a similar posterior to the uterus with pedicle attached to the posterior wall of
the uterus (marked by white star in C)—FIGO class 7 pedunculated subserosal fibroid. ( D) T2 sagittal MR image shows a well-encapsulated
heterogeneous lesion arising from the fundus of the uteru s with hyperintense areas within (marked by white star in D)—FIGO class 7
pedunculated subserosal fibroid with degeneration. ( E) T2 axial magnetic resonance imaging (MRI) image shows a well-de fined pedunculated
intracavitary lesion with pedicle attached to left lateral wall (marked by white star in E)—FIGO class 0 submucosal fibroid (abnormal uterine
bleeding [AUB]-L SM,O ).
Journal of Gastrointestinal and Abdominal Radi ology ISGAR Vol. 9 No. 1/2026 © 2026. The Author(s).
Imaging in Abnormal Uterine Bleeding Renganathan et al. 61
malignancies or are at extremely high risk of developing
invasive cancers. 31
The fundamental etiology of these hyperplasias is a
hormonal imbalance with unopposed estrogen stimulation
and simultaneously inadequate progesterone levels. Some
of the conditions which result in this underlying imbalance
are polycystic ovarian syndrome, metabolic syndrome,
nulliparity, tamoxifen therapy, corpus luteum insuf ficiency,
Lynch syndrome, or improper hormonal supplementa-
tion in postmenopausal patients.
32 Also, about one-
third of endometrial carcinomas are known to begin as
hyperplasias.
30
Accordingly, management of hyperplasia without atypia
is based on conservative measures with lifestyle modi fica-
tions and oral contraceptives spearheading the management
protocol, with rare cases requiring preventive hysterectomy.
Contrarily, patients with atypical hyperplasia and endome-
trioid intraepithelial neoplasia are candidates for upfront
total hysterectomy, with very rare indications for conserva-
tive management.
32
Certain other nonendometrial etiologies are also known
to present as AUB. One such is carcinoma of the cervix, which
is usually seen in middle-aged women, usually with certain
high-risk factors and known to commonly present as IMB or
post-coital bleeding. There are also other malignancies, such
as leiomyosarcoma (secondary malignant transformation of
uterine fibroids), which are also known to present with AUB
with associated sudden interval increase in size of the
fibroid.
25
Imaging
Ultrasound
Utilization of US has become an indispensable component of
routine gynecological assessment. 33 More so, when it comes
to detailed evaluation of the uterus, especially the endome-
trium, higher resolution and a more dynamic and focused
imaging is necessary with use of transvaginal sonography.
The endometrial thickness is the primary feature that
points to endometrial hyperplasia in the absence of an
obvious lesion. The limit beyond which the endometrial
thickness is considered pathological differs according to
the menstrual status and phase of the menstrual cycle as
detailed in
►Fig. 7 .33–35
A more streamlined US evaluation and interpretation
algorithm of the endometrium has been put forth with the
use of the consensus opinion from the International Endo-
metrial Tumor Analysis (IETA) group aiding in predicting the
risk of different endometrial pathologies.
36 In addition to the
quantification of the endometrial thickness, the following
other aspects are also to be assessed:
(1) Endometrial thickness
(2) Echogenicity/uniformity
(3) Midline
(4) Outline
(5) Color score
(6) Vascular pattern
(7) Endomyometrial junction
MRI
MRI is an extremely sensitive modality with excellent
soft tissue resolution that helps to better delineate the
endometrium and the adjacent JZ. This is most bene ficial in
the assessment of malignancies and gauging the extent of
deeper uterine in filtration. The regular protocol consists of
T2-weighted, T1-weighted, diffusion-weighted imaging,
and dynamic postcontrast images with axial, coronal, and
sagittal planes planned in line with the endometrial
alignment.
37
The uterine anatomy is best appreciated on a T2-weighted
image and is homogeneously T2 hyperintense, surrounded
by a low-signal intensity JZ and intermediate-signal intensity
myometrium.
37
Contrast enhancement is usually a relative assessment of
the myometrium, and myometrial enhancement usually
varies with the phase of the menstrual cycle. The postmeno-
pausal endometrium and myometrium are usually atrophic
with an indistinct JZ.
37 A thickness of 4 mm with no focal
changes is usually considered normal for a postmenopausal
woman with a < 1% risk of development of cancer.
Fig. 7 Endometrial thickness in various age grou ps and various phases of menstrual cycle.
Journal of Gastrointestinal and Abdominal Radio logy ISGAR Vol. 9 No. 1/2026 © 2026. The Author(s).
Imaging in Abnormal Uterine Bleeding Renganathan et al.62
Preoperative pelvic MRI is known to have a moderate sensi-
tivity and speci ficity in identifying invasion to the myome-
trium in endometrial cancer and a rather weak predictive
value when used to assess the absence of myometrial inva-
sion, thus guiding in triaging and managing endometrial
neoplasia.
38 ►Figs. 8 and 9 show the US and MRI of simple
endometrial hyperplasia without atypia and endometrial
carcinoma, respectively. ►Table 5 summarizes the reporting
checklist for structural causes of AUB.
Coagulopathy (AUB-C)
The term “coagulopathy” denotes a systemic disorder that
impairs hemostasis. It is estimated that approximately 13% of
women who suffer from bleeding disorders exhibit
Fig. 8 Transvaginal ultrasound ( A) and magnetic resonance imaging (MRI) images ( B) show diffuse thickening of endometrium with preserved
endomyometrial junction (marked by black arrows in A) and regular midline (marked by white arrow in B). Histopathology was simple
endometrial hyperplasia without atypia (abnormal uterine bleeding [AUB]-M).
Fig. 9 Transvaginal ultrasound ( A and B) and Doppler images of a patient with postmenopausal bleeding showing an irregular isoechoic mass
within the endometrial cavity (marked by white star in A and B) with indistinct endomyometrial juncti on in the posterior aspect (marked with
black arrows) with multifocal vascularity and a color score of 4 (marked by white arrows in C). Note the preserved endomy ometrial junction in the
anterior aspect (marked by white arrows in B). T2 sagittal ( D) and postcontrast T1 fat-saturated magnetic resonance imaging (MRI) images ( E and
F) show a heterogeneously enhancing mass within the endometrial cavity with myometrial invasion (marked by white arrows in D)a n d
interruption of subendometrial enhancement in the posterior aspect (marked by black arrows in E and F)—consistent with myometrial invasion
(abnormal uterine bleeding [AUB]-M).
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Imaging in Abnormal Uterine Bleeding Renganathan et al. 63
menorrhagia, with von Willebrand disease identi fied as the
most prevalent condition contributing to this phenome-
non.39 Furthermore, patients who are undergoing anticoag-
ulant therapy often present with AUB, particularly in the
form of heavy menstrual bleeding (HMB). The frequency
with which these coagulopathies contribute to AUB in
symptomatic women remains uncertain. Nevertheless, it is
imperative to take these conditions into account when
assessing patients with AUB, particularly in the absence of
underlying pelvic pathologies.
3
Ovulatory Disorders (AUB-O)
Ovulatory disorders represent a common etiology of AUB
and arise from episodic or chronic dysfunction of the hypo-
thalamic -pituitary-ovarian axis.40 These disorders are char-
acterized by unpredictable menstrual bleeding patterns and
varying degrees of flow. The clinical manifestations can differ
significantly, ranging from amenorrhea to infrequent or light
bleeding, as well as episodes of unpredictable and excessive-
ly HMB that may necessitate medical intervention. In certain
instances, AUB associated with ovulatory disorders is attrib-
uted to the absence of regular cyclic production of proges-
terone from the corpus luteum due to anovulation, or
irregular ovulations resulting from luteal out-of-phase follic -
ular events occurring in the later stages of reproductive
years.
41
Diagnosis of ovulatory disorders is often achievable
through a comprehensive assessment of menstrual history
and clinical presentation. Presenting symptoms may include
delayed menarche, infrequent or irregular menstruation,
primary or secondary infertility, and hirsutism. Additional
diagnostic methods for ovulatory disorders include the
measurement of basal body temperature, the use of ovula-
tion predictor kits to assess urine luteinizing hormone levels,
and the evaluation of progesterone levels.
Upon con firming the presence of an ovulatory disorder,
the subsequent step involves categorizing the disorder into
one of the four primary classi fications as delineated by
the FIGO classi fication system for ovulatory disorders.
The secondary classi fication re fines the identi fication of
the speci fic type of abnormality within a designated ana-
tomical category, while the tertiary classi fication elucidates
Table 5 Reporting checklist for structural causes of AUB
Polyp (AUB-P) Dimension
Location
Number
Morphology
Adenomyosis (AUB-A) MUSA features - Direct and indirect features
Location (anterior/poster ior/lateral wall/fundal)
Differentiation - Focal/Diffuse/Mixed ( > 25% myometrium/ < 25%)
Cystic/noncystic
Uterine layer involvement (JZ/middle/outer myometrium)
Disease extent (mild/moderate/severe)
Measurement of lesion size - The Largest dimension of the largest lesion
Leiomyoma (AUB-L) Classi fication
Total uterine volume
No of leiomyoma (1/2/3/4/ > 4)
Volume of up to 4 leiomyoma
Location – Ant/post/lat/central, vertical plane – upper/lower half/both
Endometrial contact
Endometrial malignancy/hyperplasia
(AUB-M) - Based on International
Endometrial Tumor Analysis (IETA)
Endometrium:
Thickness
Echogenicity/Uniformity
Midline
Outline
Color score
Vascular pattern
EMJ
Intracavitary fluid:
Thickness and echogenicity
Intracavitary lesion:
Total endometrial thickness and three dimensions
Extent
Echogenicity
Outline
Color score
Vascular pattern
Bright edge
Synechiae
Abbreviations: AUB, abnormal uterine bleeding; JZ, junctional zone; MUSA, Morphological Uterus Sonographic Assessment; EMJ, endo myometrial
junction.
Journal of Gastrointestinal and Abdominal Radio logy ISGAR Vol. 9 No. 1/2026 © 2026. The Author(s).
Imaging in Abnormal Uterine Bleeding Renganathan et al.64
the speci fic causative factors contributing to the ovulatory
disorder.6 ►Table 6 shows the FIGO ovulatory disorders
classification.
Utilizing the modified Rotterdam criteria, the diagnosis of
PCOS may be established if at least two of the following
criteria are met: (1) evidence of clinical or biochemical
hyperandrogenism, (2) indications of oligoanovulation, and
(3) observation of polycystic ovarian morphology via US,
after ruling out other relevant conditions. The US criteria for
diagnosing polycystic ovarian morphology include the pres-
ence of a minimum of 20 follicles per ovary and an ovarian
volume of at least 10 cm
3. ►Fig. 10 shows polycystic ovarian
morphology in US. This diagnosis is typically made through
transvaginal ultrasonography employing a transducer fre-
quency of 8 MHz or greater. 40 Usage of simple, easily avail-
able, and cost-effective modality such as US in evaluation of
ovulatory dysfunction helps in identifying the ovarian etiol-
ogy and thereby improves the clinical acumen.
Endometrial (AUB-E)
In instances where identi fiable causes for AUB are not
apparent, local endometrial pathologies may be in fluencing
endometrial hemostasis. The etiology typically involves hor-
monal imbalances within the uterus. A local de ficiency of
vasoconstrictors, such as endothelin-1 and prostaglandin
F2α, may result in excessive bleeding by promoting the
production of plasminogen activators, which facilitate the
lysis of blood clots.
42 Concurrently, there tends to be an
increased synthesis of prostaglandin E2 and prostacyclin (I2),
both of which serve as potent vasodilators and possess
antiplatelet aggregation properties.
43
In addition to local hormonal disturbances, various con-
ditions may contribute to AUB, presenting as IMB or pro-
longed menstrual bleeding. These conditions may include
infections and in flammatory processes in the endometrium,
such as chronic endometritis; however, the precise mecha-
nisms underlying these conditions remain poorly under-
stood.44 For women with normal ovulatory function, the
diagnosis of local endometrial pathology as a causative factor
for AUB is generally established through a process of exclu-
sion, occurring only when no structural causes have been
identified.
Iatrogenic (AUB-I)
Iatrogenic factors contributing to AUB include intrauterine
devices (IUDs) and various medications. Breakthrough
bleeding (BTB) refers to unscheduled bleeding during treat-
ment with gonadal steroids, such as estrogens and proges-
tins, which are primarily used as contraceptives in oral,
transdermal, vaginal, or injectable forms. BTB often occurs
due to decreased levels of these steroids resulting from poor
adherence to the medication regimen.
Additionally, certain medications, including tricyclic anti-
depressants and phenothiazines, can alter dopamine metab-
olism by decreasing serotonin uptake, leading to reduced
inhibition of prolactin release. This may result in anovulation
and irregular vaginal bleeding.
3
Certain IUDs, particularly the levonorgestrel intrauterine
system, may also induce unscheduled vaginal bleeding with-
in the initial 3 to 6 months of use, potentially leading to
premature removal of the device. 45
Not Yet Classi fied (AUB-N)
The conditions categorized within this group include chronic
endometritis, arteriovenous malformations, isthmocele
(►Fig. 11 ), and myometrial hypertrophy. The role of these
conditions in AUB remains inadequately de fined, necessitat-
ing their classification in this category. It is essential to gather
Fig. 10 Transvaginal ultrasound images of a patient with irregular cycles show enlarged right ( A)a n dl e f t(B) ovaries (marked by white stars in A
and B,r e s p e c t i v e l y )w i t hv o l u m e> 10 mL, thickened stroma, and multiple small < 9 mm peripherally arranged follicles (abnormal uterine
bleeding [AUB]-O, TYPE IV, polycystic ovary syndrome [PCOS]).
Table 6 FIGO ovulatory disorders classi fication system
Primary classification Secondary classification
Type I:
Hypothalamic
Genetic
Autoimmune
Iatrogenic
Neoplasm
Functional
Infectious/In flammatory
Trauma/Vascular
Physiological
Idiopathic
Endocrine
Type II:
Pituitary
Type III:
Ovarian
Type IV:
PCOS
Diagnosed and classi fied
as recommended by the
sinternational PCOS network
Abbreviations: FIGO, International Federation of Gynecology and Ob-
stetrics; PCOS, polycystic ovary syndrome.
Journal of Gastrointestinal and Abdominal Radi ology ISGAR Vol. 9 No. 1/2026 © 2026. The Author(s).
Imaging in Abnormal Uterine Bleeding Renganathan et al. 65
further evidence in the future to appropriately assign these
conditions to a more accurate classi fication.3
►Fig. 12 summarizes the clinical and imaging approach to
AUB.
Conclusion
Standard terminologies, de finitions, and structured imaging
methodologies are essential for the accurate identi fication of
the causes of AUB, facilitating effective management, enhancing
patient outcomes, and supporting clinical research efforts. US
represents the initial diagnostic modality of choice for patients
presenting with AUB, owing to its widespread availability and
capability to assess the endometrium, myometrium, and ad-
nexal structures. Additionally, sonohysterosalpingography can
provide further evaluation of the endometrial cavity and lining.
MRI offers superior contrast for soft tissues, serving as a
valuable tool for complex problem-solving.
The role of imaging evaluation is pivotal in differentiating
between structural and nonstructural etiologies of AUB.
Structured reporting using PALM-COEIN with imaging
checklists ensures consistent communication with gynecol-
ogists and improves patient outcomes.
Funding
None.
Conflict of Interest
None declared.
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