Introduction
Endometriosis is a gynecologic disorder in which endo -
metrial-like tissue is found outside the uterine lining, often
associated with inflammation [1]. The clinical presentation
is variable, with pelvic pain comprising the most frequent
symptom across all age groups. In the adolescent popula -
tion, endometriosis is often overlooked as a cause of pel -
vic pain because of limited awareness by caregivers as well
as a confusing clinical picture, where patients may pres -
ent with cyclical and acyclical pain. This combination of
factors may lead to a delay in diagnosis, which can have
considerable clinical implications, such as persistent pain,
central sensitization, and potential infertility. Adolescents,
generally considered between the ages of 10 and 19 years,
are a unique patient cohort in that they have started puberty
but are not yet adults. The adolescent population may feel
uncomfortable discussing symptoms or may consider their
symptoms normal. Additionally, adolescents are more likely
than previously thought to develop deep endometriosis, a
severe form of endometriosis involving tissues below the
peritoneum.
Although the diagnosis of endometriosis in adults is often
confirmed by laparoscopy, there has been increased empha-
sis on diagnosis and surgical planning via imaging in recent
years [2]. In the adult population, transvaginal ultrasound
is considered the first-line imaging technique for clinically
suspected endometriosis, with magnetic resonance imaging
(MRI) reserved as a second-line imaging study to confirm
the diagnosis and for treatment planning [ 3]. In contrast,
in the adolescent population, transabdominal ultrasound
is the first-line imaging technique for pelvic pain. Many
adolescents who are not sexually active may feel uncom -
fortable undergoing transvaginal ultrasound, although it
is not contraindicated in the nonsexually active patient. A
transabdominal ultrasound can be helpful for the identifica-
tion of ovarian endometriomas but has a limited role in the
evaluation of deep pelvic endometriosis. Therefore, in these
patients, MRI is playing an increasingly important role in
diagnosis [4, 5]. This paper discusses the nuances associ -
ated with the clinical and imaging diagnosis of suspected
endometriosis in adolescents.
Presentation
Endometriosis is a chronic condition in which ectopic endo-
metrial glands and stroma are found outside of the uterus.
It is the most common cause of secondary dysmenorrhea
in adolescents. In a review by Janssen et al. [ 6], 70% of
adolescents undergoing laparoscopy for dysmenorrhea
unresponsive to nonsteroidal anti-inflammatory drugs
and suppressive hormone therapy were diagnosed with
endometriosis.
Endometriosis can present with a broad spectrum of
symptoms. Classically, the adult patient experiences severe
dysmenorrhea associated with luteal phase symptoms of
pelvic pain. However, patients can have symptoms ranging
from chronic daily pain to dyspareunia, cyclic bowel and
bladder symptoms, and infertility. In adolescents, noncyclic
pain or pain between periods is a common complaint. In
one retrospective study, more than 90% of adolescents with
endometriosis complained of acyclic pain, and 62% com -
plained of both acyclic and cyclic pain [7]. Other symptoms
may include irregular heavy periods, dyspareunia, and nau-
sea. Adolescents and young adults less than 24 years of age
are far more likely to report higher pain scores than older
patients [8].
Diagnostic delay
Diagnostic delay is common in adolescents and is driven
by factors involving patients and clinicians. Of note, ado -
lescents wait three times longer than adults to seek medi -
cal care [ 9]. Many factors lead to adolescents normalizing
the degree of pain they are experiencing. Young adolescents
often experience embarrassment and will not commonly
share information about their periods with family or friends.
They do not realize that the degree of pain they are expe -
riencing is abnormal and are led to believe that menstrual
cramps are an expected part of the menstrual cycle through
societal norms. When clinicians obtain a medical history
from an adolescent, it is important to determine the extent
to which this pain is interfering with school and extracur -
ricular activities, as absenteeism is noted to be much higher
in adolescents with endometriosis [ 8]. Their quality of life
is dramatically impacted, leading to poor socialization and
concern for isolation at a particularly vulnerable time of
their lives. Adolescents with endometriosis are more likely
to report mental health issues such as anxiety and depres -
sion, the use of pain medications, and the avoidance of exer-
cise [10].
Clinicians are less likely to consider a diagnosis of endo-
metriosis in adolescents than in adults. The difference in
clinical presentation and lack of specific findings on pelvic
examination and ultrasound often mislead the clinician.
The pelvic examination in adolescents with endometriosis
is often relatively benign compared to the pelvic examina -
tion in adults with endometriosis, which is more likely to
reveal a pelvic mass or nodularity. Additionally, the com -
mon site of disease, the posterior cul-de-sac and uterosacral
ligaments, can be challenging to evaluate on physical exam,
particularly in patients who have not been sexually active.
Thus, clinicians are less likely to order pelvic ultrasound
1 3
4845
Abdominal Radiology (2025) 50:4844–4853
examinations for adolescents and are more reluctant to rec -
ommend diagnostic laparoscopy, which could be perceived
as a relatively aggressive diagnostic measure in such young
individuals. However, laparoscopy is paramount for diag -
nosis in this population, as most endometriosis lesions in
these patients are superficial and not likely to be noted via
imaging studies. In addition, endometriosis lesions in ado -
lescents often do not have the classic powder-burn, black or
brown endometrial tissue, on direct visualization by lapa -
roscopy and therefore can easily be missed by Gynecologic
surgeons. These atypical lesions, often presenting as clear,
white, or small hemorrhagic lesions, produce high levels of
prostaglandins and substantial pain [8, 11].
Diagnostic imaging considerations
The need for imaging should be determined by both his -
tory and physical examination, as imaging is not routinely
needed in a patient with mild dysmenorrhea. Evaluation
of the adolescent with symptoms of endometriosis should
begin with a detailed history regarding the type and loca -
tion of pain, cyclic association, a positive family history of
endometriosis, a history of obstructive genital malforma -
tions, early menarche, short menstrual cycles, and the use
of contraceptives to treat severe dysmenorrhea, as well as
inciting factors [11, 12].
Standard imaging evaluation for the adolescent patient
with concern for endometriosis should begin with a trans -
abdominal pelvic ultrasound examination, which is consid -
ered first-line imaging, particularly in young patients who
are not sexually active. Although transabdominal ultrasound
is limited in its evaluation of endometriosis, it may exclude
other causes of pain such as adnexal masses or congenital
anomalies [8]. Additionally, transabdominal ultrasound may
identify some forms of endometriosis, including endome -
triomas; however, these are a less common manifestation of
endometriosis in the adolescent population.
After a transabdominal ultrasound examination has been
performed, one may consider performing a transvaginal
ultrasound (TVUS). Although this technique is superior to
transabdominal ultrasound in its evaluation of the female
pelvis and specifically in identifying endometriosis, it is a
sensitive procedure that may be considered in the adoles -
cent after considerable thought and care. Transvaginal ultra-
sound is less commonly used in adolescent patients who are
not sexually active and may cause anxiety and discomfort
even in those who are sexually active; however, as a gold-
standard technique, it can still be offered to women of repro-
ductive age after a discussion of risks and benefits. In some
circumstances, transrectal or transperineal ultrasound may
be considered in nonsexually active patients [ 13]. Table 1
outlines standard transabdominal and transvaginal ultra -
sound protocols for the evaluation of endometriosis.
Given the limited value of transabdominal ultrasound in
the evaluation of deep endometriosis and the potential con -
cerns associated with transvaginal ultrasound, MRI is a help-
ful tool in the evaluation of adolescents with dysmenorrhea.
With appropriate preparation, most adolescents are able to
tolerate MRI and do not require anesthesia. Furthermore,
adolescent patients with endometriosis are more likely to
develop deep endometriosis than previously thought, which
is better evaluated with MRI than Ultrasound. MRI is non -
invasive and provides excellent soft tissue detail without
radiation [14]. MRI of the pelvis may be performed without
or with intravenous (IV) contrast in adolescents; adoles -
cent patients can generally tolerate the placement of an IV
catheter. Vaginal contrast (aqueous gel) has been shown to
improve the detection of endometriosis, particularly that of
deep endometriosis, but the use of this contrast may be con-
sidered uncomfortable or invasive by adolescent patients
[5]. Patients are asked to self-insert the gel before imaging,
but if they refuse or are unable to insert the contrast, MRI
may still be performed [ 5]. Fasting for at least 4 h prior to
imaging and/or intestinal peristalsis agents may be helpful
to decrease bowel motion artifact [15]. Table 2 summarizes
the full MRI protocol commonly used to evaluate endome -
triosis. An abbreviated protocol, utilizing volumetric T2-W
3D SPACE and T1-W Vibe Dixon axial pre-contrast fat
saturated images, has also been suggested in the evaluation
of endometriosis as the disease often occurs in a predictable
pattern. The abbreviated protocol may be useful in younger
patients or those with anxiety and can help decrease overall
throughput time [15].
Ultimately, if imaging is negative and patients are refrac-
tory to clinical treatment, the reference standard for the
diagnosis of endometriosis in adolescent patients remains
laparoscopy, with diagnosis and treatment occurring at the
same time. Imaging, however, assists in earlier diagnosis
and treatment of adolescent patients, who traditionally expe-
rience delays in diagnosis as well as aids in preoperative
Table 1 Transabdominal and transvaginal ultrasound protocols for the
evaluation of endometriosis
Pelvic structure Planes Comment
Uterus Longitudinal and Transverse
Endometrium Longitudinal With
Cine
Ovaries and adnexa Longitudinal and Transverse With or
without
Doppler
Bladder Longitudinal and Transverse
Cul de sac and poste-
rior compartment*
Longitudinal and Transverse Cine slid-
ing sign
*Transvaginal protocol only
1 3
4846
Abdominal Radiology (2025) 50:4844–4853
of patients aged 18 to 20 years. Rectosigmoid lesions were
not seen in any patients younger than 15 years, and no blad-
der or ureter lesions were identified in their cohort. Ovarian
endometriomas were observed in 20.7% of the patients in
this study [17].
Superficial endometriosis is defined as endometrio -
sis along the surface of the peritoneum or organs without
subperitoneal extension. These lesions are reliably identi -
fied by laparoscopy but not routinely identified on imaging
studies. There is evidence that superficial endometriosis
can be identified on transvaginal ultrasound examinations
as hypoechogenic nodules measuring less than 5 mm in
characteristic locations such as along the uterosacral liga -
ments, but detection of such nodules is operator dependent,
and identification of superficial endometriosis by trans -
abdominal ultrasound has not been described. With MRI,
superficial disease can be identified as hyperintense foci in
characteristic locations on T1-weighted (T1W) images [18].
Ovarian endometriomas are ovarian cystic lesions that
contain blood products of variable age. When present, these
endometriomas can be identified by characteristic imaging
features on ultrasound examinations and MRI as described
by the American College of Radiology (ACR) Ovarian
Reporting and Diagnosis System (O-RADS). On ultrasound
examinations, lesions can be unilocular or may contain a
few internal septa. Endometrioma cyst fluid has character -
istic homogeneous, low-level echoes, sometimes referred to
as ground-glass echoes. The inner walls of the cyst should
be smooth, and punctate echogenic foci may be observed
within the wall. There should be no vascular flow on Dop -
pler imaging within an endometrioma (Figs. 1a-c and 2a and
b) [19]. On MRI, endometriotic cyst contents are homoge -
neously hyperintense on T1W images. Endometriotic cyst
fluid is hypointense or intermediate on T2-weighted (T2W)
images, often referred to as “T2 shading,” which can appear
as homogeneous or graduated. On T2W images, endome -
triomas may have hypointense nodules or linear mural foci
that do not enhance. Endometriomas show variable diffu -
sion signal. Septa may be present but should not enhance
(Figs. 1e and 2c and d) [20].
Deep endometriosis is typically multifocal but tends to
occur in characteristic locations in the pelvis. The utero -
sacral ligaments, which are paired uterine suspensory liga -
ments that extend from the torus uterinus (posterior cervix)
posteriorly to the sacrum, are the most common location of
deep endometriosis during adolescence (Fig. 2e).
Deep endometriosis lesions are not reliably seen on
transabdominal ultrasound studies, but the diagnosis of
deep endometriosis by transvaginal ultrasound has been
well described [21, 22] and typically focuses on identifica -
tion of direct or indirect imaging findings of endometriosis.
Direct imaging findings are sonographic observations that
management which may require a multidisciplinary team in
more severe cases.
Imaging findings
It is known that endometriosis phenotypes evolve through -
out a patient’s lifetime. Although adolescents may present
with superficial endometriosis, deep endometriosis, or ovar-
ian endometriomas, the proportion of superficial disease is
greater in adolescent patients, with the proportion of deep
endometriosis and endometriomas increasing after age 24
[16]. An MRI study of endometriosis in patients aged up
to 20 years found that the prevalence of endometriosis on
MRI increased linearly with age [ 17]. In this study, retro -
cervical lesions (uterosacral ligaments and posterior vagina)
were seen in 4.7% of patients aged younger than 15 years,
in 30% of patients aged 15 to 18 years, and in up to 65%
Table 2 MRI protocol for the evaluation of endometriosis
Sequence Plane slice
thick-
ness
(mm)
comment
T2WI TSE Axial 3–5 Small FOV for
female pelvis
Coronal
and/or
sagittal
4 Large FOV
T1WI in-phase and
out-of-phase
GRE or Dixon
Axial 2–3 Large FOV
T1WI with fat suppression
non-contrast
Axial 4 Small FOV for
female pelvis
Sagittal 3–4 Large FOV
T1WI with IV contrast Axial 3 Small FOV , Sub-
traction images
Sagittal 3–4 Large FOV , Sub-
traction images
Diffusion-weighted Imaging Axial 4–5 b values = 0, 50,
1000 s/mm2
T1WI pre-three-dimen-
sional fast spoiled GRE
with fat suppression
Coronal
Sagittal
1 Optional of
upper abdomen
T2WI FRFSE with fat
saturation
Coronal
Sagittal
5 Optional of
upper abdomen
T2WI fast-spin echo-planar
fast spin echo
Coronal Large FOV to
include kidneys
T2WI fast spin echo with
fat saturation
Axial Large FOV
Adapted from VanBuren W, Feldman M, Shenoy-Bhangle AS,
Sakala MD, Young S, Chamie LP, Giudice L, Hindman NM, Tong A,
Rabban JT, Yano M, Kilcoyne A, Dave HD, Poder L, Kho RM, Bur -
nett TL, Khan Z, King C, Shen L, Colak C, Burk KS, Andrieu PIC,
Franco IVP, Glanc P, Kielar AZ, Taffel MT, Kania LM, Bonde A,
Pectasides M, Arif-Tiwari H, Laifer-Narin S, Nicola R, Jha P (2024)
Radiology State of the art Review: Endometriosis Imaging Interpre -
tation and Reporting. Radiology 312:e233482. h t t p s : / / d o i . o r g / 1 0 . 1 1 4 8
/ r a d i o l . 2 3 3 4 8 2
1 3
4847
Abdominal Radiology (2025) 50:4844–4853
hyperintense foci on T1W or T2W images; such foci are
thought to correspond to areas of glandular endometrium-
like tissue [ 23]. The retrocervical area (including the torus
uterinus, uterosacral ligaments, and posterior vaginal wall)
is the most common site of deep endometriosis in adoles -
cents. While no consensus exists, the uterosacral ligaments
are probably normal when less than 3 mm in thickness and
indeterminate when 3–5 mm in thickness. The ENDO -
V ALIRM group described diagnostic criteria for proximal
uterosacral ligament disease (within 2 cm of the torus ute -
rinus), including regular or irregular uterosacral ligament
thickening (> 5 mm), nodules along the ligament that are
visible in 2 planes, irregular retraction of the ligaments, and
hemorrhagic foci along the uterosacral ligaments regardless
of the presence of thickening (Fig. 3) [24]. Rectosigmoid
deep endometriosis has also been reported at low rates in
adolescents [17] This type of deep endometriosis is often
contiguous with retrocervical disease and can characteristi -
cally cause a thickening of the rectosigmoid wall that has a
fan shape or “mushroom cap” appearance.
correspond with ectopic endometrial-like tissue in charac -
teristic locations for endometriosis such as the uterosacral
ligaments, uterine serosa, rectosigmoid region, bladder,
and vagina. These lesions are typically hypoechoic nodules
or areas of hypoechoic thickening with smooth or irregu -
lar/spiculated borders. Hyperechoic or cystic foci may be
observed within the lesions. Indirect findings are sono -
graphic observations that are a result of deep endometrio -
sis implants but do not correspond with the lesions directly.
Indirect observations may include fixed uterine retrover -
sion, abnormal position of the ovaries, and tethering of
bowel loops to the uterus [2]. Sliding maneuvers performed
along the posterior uterine wall and rectum, along the ante -
rior uterine wall and bladder and at the level of both ovaries
can also provide indirect evidence of endometriosis when
abnormal sliding between structures is observed [2].
Deep endometriosis in adolescents is typically diagnosed
on MRI. Imaging findings of deep endometriosis on MRI
have been well described. On T2W images, deep endometri-
osis lesions are hypointense compared to muscle. The lesions
may be nodular or may manifest as thickening along struc -
tures, and the surface of the lesions can be smooth or irregu-
lar/stellate. The lesions may or may not be accompanied by
Fig. 1 18 year-old woman with left-sided pelvic pain. a The ovaries
were not identified by transabdominal ultrasound technique. b, c The
patient was amenable to transvaginal ultrasound which showed a uni -
locular left ovarian cystic lesion with homogeneous low-level inter -
nal echoes and no internal vascular flow with color Doppler. d The
lesion shows characteristic T2 shading on T2W MR image (solid white
arrow) with a peripheral dark spot (dashed white arrow). e The lesion
shows characteristic homogeneous hyperintense signal on T1W image
with fat suppression. Patient underwent laparoscopy 2 months later
with cystectomy of the endometrioma. Superficial endometriosis was
noted in the posterior cul-de-sac
1 3
4848
Abdominal Radiology (2025) 50:4844–4853
Treatment
Treatment strategies for endometriosis include both medical
and surgical modalities and often require a multi-modal and
multidisciplinary approach.
Hormonal management
Hormonal suppression with combined hormonal contra -
ceptives or progestins remains the cornerstone of medical
therapy for the management of endometriosis and should
typically be used as initial therapy for primary dysmenor -
rhea. Medical management should be considered suppres -
sive and not curative as it will not resolve endometriomas
or deep disease but suppresses ovulation and creates a local
hypoestrogenic state, which may prevent the development
or growth of endometriomas. Of note, although the use of
oral contraceptives may improve symptoms, it does not
prevent the progression of deep disease or the possibility
of future infertility [12]. The treatment choice is dependent
on various factors, including lifestyle, comorbidities, tol -
erability (i.e., ability to swallow pills), and willingness to
trial medications. Combined oral contraceptives are often
first-line therapy as they are typically well tolerated and
Endometriosis and congenital female
reproductive tract anomalies
Endometriosis is known to occur in conjunction with con -
genital female reproductive tract anomalies and has been
found in association with all forms of Mullerian anomalies
[25]. A recent meta-analysis demonstrated that the rate of
endometriosis was significantly higher (47%) among those
with obstructive Mullerian anomalies than among those with
Mullerian anomalies that were not associated with obstruc -
tion (19%) [ 26]. This study also demonstrated slightly
higher rates of endometriosis among those with nonobstruc-
tive Mullerian anomalies (23%) than among those without
anomalies (21%). The diagnostic appearance and imaging
criteria for ovarian endometriomas and deep endometrio -
sis do not differ in the setting of congenital reproductive
tract anomalies (Fig. 4). If a pelvic mass or genitourinary
malformation is identified, the suspicion for an obstructive
Mullerian anomaly and associated endometriosis should
be heightened. It is unknown if there are differences in the
location of deep endometriosis among individuals with such
anomalies.
Fig. 2 Images from a 19-year-old patient with chronic pelvic pain, dys-
pareunia, and a family history of endometriosis. a Transvaginal ultra-
sound image through the right ovary shows 2 small cystic structures
with low-level internal echoes characteristic of endometriomas (white
arrows with closed arrowheads). b Image through the right ovary with
color Doppler shows no vascular flow within the lesions (white arrows
with closed arrowheads). Pelvic MRI was performed 9 months later.
c T2W axial image shows one of the 2 endometriomas with T2 shad -
ing and a dark spot sign (black arrow). d The lesion shows charac -
teristic homogeneous hyperintense signal on the corresponding axial
T1W image (dashed arrow). e Coronal T2W image through the torus
uterinus/uterosacral ligaments shows asymmetric, irregular thickening
of the right uterosacral ligament (white arrows with open arrowheads).
Oral contraception was initiated after imaging
1 3
4849
Abdominal Radiology (2025) 50:4844–4853
Fig. 4 Images from a 22-year-old patient with a known Mullerian
anomaly and pelvic pain. a Oblique coronal T2W image through the
pelvis shows a unicornuate right uterus communicating with the cervix
(not shown). A left uterine remnant with functional endometrial tissue
(thin arrow) with no communication to the cervix or vagina can also be
seen. b Axial T1W image shows a right ovarian endometrioma (thick
arrow). A T1 hyperintense focus in the left ovary corresponds to a cor-
pus luteum (dashed arrow). Treatment with hormone suppression was
initiated. Endometriosis was confirmed on appendectomy
Fig. 3 Images from a 15-year-old
patient with chronic pelvic pain,
dysmenorrhea, and menorrhagia.
The patient’s mother had a his-
tory of endometriosis. a, b Sagit-
tal T2W images show a hypoin-
tense nodule along the proximal
right uterosacral ligament (white
dashed arrow) and asymmetric,
irregular thickening along the
length of the right uterosacral
ligament (solid white arrow). c
Axial T2W image shows that
the right uterosacral ligament is
also thickened in the axial plane
(solid white arrow). d Sagittal
image through the left uterosacral
ligament for comparison shows
the ligament to be smooth with
no nodules (black arrows). No
other sites of deep endometriosis
were identified. The ovaries (not
shown) were normal in appear-
ance with no endometrioma.
Treatment with continuous oral
contraceptive pills was initiated
after imaging
1 3
4850
Abdominal Radiology (2025) 50:4844–4853
The controversy between laparoscopic ablation versus
excision of endometriosis lesions exists because of the
paucity of high-quality data in the adolescent population.
Excision of lesions is the preferred method for removal
and allows for pathologic confirmation, confirmation of
complete removal down to the level of normal tissue, and
removal over critical structures, including the bowel, blad -
der, and ureter. If a patient undergoes general anesthesia for
a laparoscopy, it is important to consider the option of con-
current levonorgestrel-releasing intrauterine device inser -
tion for post-operative hormone therapy, as intraoperative
insertion may negate the need for a painful office procedure
for the adolescent patient. Postoperative hormone therapy
has been shown to benefit adolescents by decreasing recur -
rence and slowing disease progression. [30–32].
Adolescents with endometriosis often experience a
wide range of symptoms; the frequent overlap with mul -
tiple sources of pain, combined with a lack of awareness,
can contribute to delays in diagnosis. These pain sources
may include gynecologic conditions and non-gynecologic
causes, such as gastrointestinal disorders or musculoskeletal
issues. This complexity can make diagnosis and manage -
ment challenging, often necessitating a multi-disciplinary
approach. The treatment team may include a pain special -
ist, mental health professional, physical therapist, and
functional medicine specialist [ 33]. Complementary or
alternative treatment options such as acupuncture may assist
with chronic pelvic pain. Involving a school counselor or
social worker can be beneficial in identifying resources to
support classroom engagement and participation in extra -
curricular activities, as students with endometriosis often
face increased absenteeism.
Discussion
around fertility preservation should be priori -
tized, especially in patients with bilateral endometriomas, as
ovarian reserve can be negatively impacted postoperatively.
A thorough survey of both the pelvis and upper abdo -
men is crucial to ensure all lesions are identified. Multiple
ports are often required to allow appropriate retraction of
the uterus and adjacent structures for complete evaluation.
Careful attention should be placed on areas found to have
potential disease on imaging. Furthermore, when an endo -
metrioma is identified on imaging, there is a > 90% prob -
ability that alternate areas of endometriosis are present;
therefore, the surgeon should be prepared to address addi -
tional areas for excision. Superficial endometriosis lesions
in the adolescent population often have a unique pheno -
typic appearance, including white implants, clear vesicular
lesions, or small hemorrhagic areas on the peritoneum, as
compared to adults, who often have the characteristic red
brown lesions or black, blue, gray “powder burn” lesions.
Peritoneal pockets, also known as Allen-Master windows,
can be associated with endometriosis and should be everted
at the base and excised. Most adolescents are diagnosed
laparoscopically with early Stage I or II endometriosis, with
advanced Stage III or IV disease being less common [29].
1 3
4851
Abdominal Radiology (2025) 50:4844–4853
pelvic pain not responding to conventional therapy. J Pediatr
Adolesc Gynecol 10:199–202. h t t p s : / / d o i . o r g / 1 0 . 1 0 1 6 / s 1 0 8 3 - 3 1
8 8 ( 9 7 ) 7 0 0 8 5 - 8
8. Shim JY , Laufer MR, King CR, Lee TTM, Einarsson JI, Tyson
N (2024) Evaluation and Management of Endometriosis in the
Adolescent. Obstet Gynecol 143:44–51. h t t p s : / / d o i . o r g / 1 0 . 1 0 9 7 /
A O G . 0 0 0 0 0 0 0 0 0 0 0 0 5 4 4 8
9. Greene R, Stratton P, Cleary SD, Ballweg ML, Sinaii N (2009)
Diagnostic experience among 4334 women reporting surgically
diagnosed endometriosis. Fertil Steril 91:32–39. h t t p s : / / d o i . o r g / 1
0 . 1 0 1 6 / j . f e r t n s t e r t . 2 0 0 7 . 1 1 . 0 2 0
10. Gallagher JS, DiVasta AD, Vitonis AF, Sarda V , Laufer MR,
Missmer SA (2018) The impact of endometriosis on quality of
life in adolescents. J Adolesc Health 63:766–772. h t t p s : / / d o i . o r g /
1 0 . 1 0 1 6 / j . j a d o h e a l t h . 2 0 1 8 . 0 6 . 0 2 7
11. Shim JY , Laufer MR (2020) Adolescent Endometriosis: An
Update. J Pediatr Adolesc Gynecol 33:112–119. h t t p s : / / d o i . o r g /
1 0 . 1 0 1 6 / j . j p a g . 2 0 1 9 . 1 1 . 0 1 1
12. Chapron C, Souza C, Borghese B, Lafay-Pillet MC, Bijaoui G,
Goffinet F, de Ziegler D (2011) Oral Contraceptives and endome-
triosis: the past use of oral contraceptives for treating severe pri -
mary dysmenorrhea is associated with endometriosis, especially
deep infiltrating endometriosis. Human Reproduction 26, No.8:
2028–2035.
13. Martire FG, Lazzeri L, Conway F, Siciliano T, Pietropolli A,
Piccione E, Solima E, Centini G, Zupi E, Exacoustos C (2020)
Adolescence and endometriosis: symptoms, ultrasound signs and
early diagnosis. Fertility and Sterility 114: 0015–0282.
14. Cox M, Gould SW, Podberesky DJ, Epelman M (2016) Magnetic
resonance imaging of acquired disorders of the pediatric female
pelvis other than neoplasm. Pediatric Radiol 46: 806–817.
15. Da Silva LLC, Torres US, Torres LR, Fong MS, Okuyama FH,
Caiado AHM, Chamie LP, Moura APC, Novis MI, Warmbrand
G, D’Ippolito G (2021) Performance of imaging interpretation,
intra-and inter-reader agreement for diagnosis of pelvis endome -
triosis: comparison between an abbreviated and full MRI proto -
col. Abdominal Radiology 46:4025–4035.
16. Bourdon M, Maignien C, Marcellin L, Maitrot Mantelet L,
Parpex G, Santulli P, Chapron C (2024) Distribution of endome -
triosis phenotypes according to patients’ age in adult women with
surgical evaluation. Hum Reprod 39:2259–2267.
17. Millischer AE, Santulli P, Da Costa S, Bordonne C, Cazaubon E,
Marcellin L, Chapron C (2023) Adolescent endometriosis: preva-
lence increases with age on magnetic resonance imaging scan.
Fertil Steril 119:626–633. h t t p s : / / d o i . o r g / 1 0 . 1 0 1 6 / j . f e r t n s t e r t . 2 0 2
2 . 1 2 . 0 3 9
18. Quesada J, Härmä K, Reid S, Rao T, Lo G, Yang N, Karia S, Lee
E, Borok N (2023) Endometriosis: A multimodal imaging review.
Eur J Radiol 158:110610. h t t p s : / / d o i . o r g / 1 0 . 1 0 1 6 / j . e j r a d . 2 0 2 2 . 1 1
0 6 1 0
19. Strachowski LM, Jha P, Phillips CH, Blanchette Porter MM, Froy-
man W, Glanc P, Guo Y , Patel MD, Reinhold C, Suh-Burgmann
EJ, Timmerman D, Andreotti RF (2023) O-RADS US v2022:
An update from the American College of Radiology’s Ovarian-
Adnexal Reporting and Data System US Committee. Radiology
308:e230685. h t t p s : / / d o i . o r g / 1 0 . 1 1 4 8 / r a d i o l . 2 3 0 6 8 5
20. Reinhold C, Rockall A, Sadowski EA, Siegelman ES, Maturen
KE, Vargas HA, Forstner R, Glanc P, Andreotti RF, Thomassin-
Naggara I (2021) Ovarian-Adnexal Reporting Lexicon for MRI:
A White Paper of the ACR Ovarian-Adnexal Reporting and Data
Systems MRI Committee. J Am Coll Radiol 18:713–729. h t t p s : / /
d o i . o r g / 1 0 . 1 0 1 6 / j . j a c r . 2 0 2 0 . 1 2 . 0 2 2
21. Guerriero S, Condous G, van den Bosch T, Valentin L, Leone
FP, Van Schoubroeck D, Exacoustos C, Installé AJ, Martins WP,
Abrao MS, Hudelist G, Bazot M, Alcazar JL, Gonçalves MO,
Pascual MA, Ajossa S, Savelli L, Dunham R, Reid S, Menakaya
Author contributions B.L. wrote the abstract, introduction, diagnostic
imaging considerations, conclusion, and main text editing. M.F. orga-
nized the manuscript, wrote imaging findings, found the figures, and
edited the manuscript. M.A. wrote presentation and diagnostic delay.
C.K. wrote the section on treatment. All authors reviewed the manu -
script. Revisions perfomed by B.L. and M.F. with contribution from
C.K.
Data availability No datasets were generated or analysed during the
current study.
Declarations
Competing interests The authors declare no competing interests.
Open Access This article is licensed under a Creative Commons
Attribution 4.0 International License, which permits use, sharing,
adaptation, distribution and reproduction in any medium or format,
as long as you give appropriate credit to the original author(s) and the
source, provide a link to the Creative Commons licence, and indicate
if changes were made. The images or other third party material in this
article are included in the article’s Creative Commons licence, unless
indicated otherwise in a credit line to the material. If material is not
included in the article’s Creative Commons licence and your intended
use is not permitted by statutory regulation or exceeds the permitted
use, you will need to obtain permission directly from the copyright
holder. To view a copy of this licence, visit h t t p : / / c r e a t i v e c o m m o n s . o
r g / l i c e n s e s / b y / 4 . 0 /.
References
1. Jha P, Sakala M, Chamie LP, Feldman M, Hindman N, Huang C,
Kilcoybe A, Laifer-Narin S, Nicola R, Poder L, Shenoy-Bhangle
A, Tong A, VanBuren W, Taffel MT (2020) Endometriosis MRI
lexicon: consensus statement from the society of abdominal radi-
ology endometriosis disease-focused panel. Abdom Radiol (NY)
45:1552–1568. h t t p s : / / d o i . o r g / 1 0 . 1 0 0 7 / s 0 0 2 6 1 - 0 1 9 - 0 2 2 9 1 - x
2. Young SW, Jha P, Chamié L, Rodgers S, Kho RM, Horrow MM,
Glanc P, Feldman M, Groszmann Y , Khan Z, Young SL, Poder
L, Burnett TL, Hu EM, Egan S, VanBuren W (2024) Society of
Radiologists in Ultrasound Consensus on Routine Pelvic US for
Endometriosis. Radiology 311:e232191. h t t p s : / / d o i . o r g / 1 0 . 1 1 4 8 / r
a d i o l . 2 3 2 1 9 1
3. Feldman MK, Wasnik AP, Adamson M, Dawkins AA, Dibble EH,
Jones LP, Joshi G, Malamud K, Patel-Lippmann KK, Shampain
K, VanBuren W and Kang SK. ACR Appropriateness criteria
endometriosis. Jounral of the American College of Radiology
2024;21(11S):S384-S395. DOI h t t p s : / / d o i . o r g / 1 0 . 1 0 1 6 / j . j a c r . 2 0 2
4 . 0 8 . 0 1 7
4. Sakala MD, Jha P, Tong A, Taffel MT, Feldman MK (2023) MR
Imaging of Endometriosis of the Adnexa. Magn Reson Imaging
Clin N Am 31:121–135. h t t p s : / / d o i . o r g / 1 0 . 1 0 1 6 / j . m r i c . 2 0 2 2 . 0 6 . 0
0 6
5. El-Ali AM, Tong A, Smereka P, Lala SV (2024) MRI for endome-
triosis in adolescent patients. Pediatr Radiol. h t t p s : / / d o i . o r g / 1 0 . 1 0
0 7 / s 0 0 2 4 7 - 0 2 4 - 0 6 0 5 0 - z
6. Janssen EB, Rijkers ACM, Hoppenbrouwers K, Meuleman C,
D’Hooghe TM (2013) Prevalence of endometriosis diagnosed by
laparoscopy in adolescents with dysmenorrhea or chronic pelvic
pain: A systematic review. Hum Reprod Update 19:570–582. h t t p
s : / / d o i . o r g / 1 0 . 1 0 9 3 / h u m u p d / d m t 0 1 6
7. Laufer MR, Goitein L, Bush M, Cramer DW, Emans SJ (1997)
Prevalence of endometriosis in adolescent girls with chronic
1 3
4852
Abdominal Radiology (2025) 50:4844–4853
metaplasia pathogenic theories: a systematic review and meta-
analysis. Hum Reprod. h t t p s : / / d o i . o r g / 1 0 . 1 0 9 3 / h u m r e p / d e a e 0 8 6
27. DiVasta AD, Feldman HA, Gallagher JS, Stokes NA, Laufer MR,
Hornstein MD, Gordon CM (2015) Hormonal Add-Back Ther -
apy for Females Treated with Gonadotropin-Releasing Hormone
Agonist for Endometriosis: A Randomized Controlled Trial.
Obstetrics and Gynocology 126, No. 3: 617–627.
28. Dysmenorrhea and endometriosis in the adolescent. ACOG Com-
mittee Opinion No. 760. American College of Obstetricians and
Gynecologists. Obstet Gyneco 2018; 132: e249-58.
29. Hirsch M, Dhillon-Smith R, Cutner AS, Yap M, Creighton SM.
The prevalence of endometriosis in adolescents with pelvic pain:
a systematic review. J Pediatr Adolesc Gynecol 2020;33:623–30.
doi: h t t p s : / / d o i . o r g / 1 0 . 1 0 1 6 / j . j p a g . 2 0 2 0 . 0 7 . 0 1 1
30. Doyle JO, Missmer SA, Laufer MR. The effect of combined sur-
gical-medical intervention on the progression of endometriosis
in an adolescent and young adult population. J Pediatr Adolesc
Gynecol 2009;22: 257–263.
31. Seo JW, Lee DY , Yoon BK, Choi D. The Efficacy of Postopera-
tive Cyclic Oral Contraceptives after Gonadotropin-Releasing
Hormone Agonist Therapy to Prevent Endometrioma Recurrence
in Adolescents. J Pediatr Adolesc Gynecol 2017;30: 223–227.
32. Becker CM, Bokor A, Heikinheimo O, Horne A, Jansen F, Kiesel
L, King K, Kvaskoff M, Nap A, Petersen K, Saridogan W, Tomas-
setti C, van Hanegem N, Vulliemoz N, Vermeulen N. ESHRE
guideline: endometriosis. Human Reproductive Open, pp 1–26,
2022.
33. Greco CD. Management of adolescent chronic pelcic pain from
endometriosis: a pain center perspective. J Pediatr Adolesc Gyne-
col 2003; 16: s17-9.
Publisher’s note Springer Nature remains neutral with regard to juris-
dictional claims in published maps and institutional affiliations.
U, Bourne T, Ferrero S, Leon M, Bignardi T, Holland T, Jurkovic
D, Benacerraf B, Osuga Y , Somigliana E, Timmerman D (2016)
Systematic approach to sonographic evaluation of the pelvis in
women with suspected endometriosis, including terms, defini -
tions and measurements: a consensus opinion from the Interna -
tional Deep Endometriosis Analysis (IDEA) group. Ultrasound
Obstet Gynecol 48:318–332. h t t p s : / / d o i . o r g / 1 0 . 1 0 0 2 / u o g . 1 5 9 5 5
22. Chamie LP (2020) Ultrasound evaluation of deeply infiltrative
endometriosis: technique and interpretation. Abdom Radiol (NY)
45:1648–1658. h t t p s : / / d o i . o r g / 1 0 . 1 0 0 7 / s 0 0 2 6 1 - 0 1 9 - 0 2 3 2 2 - 7
23. VanBuren W, Feldman M, Shenoy-Bhangle AS, Sakala MD,
Young S, Chamie LP, Giudice L, Hindman NM, Tong A, Rabban
JT, Yano M, Kilcoyne A, Dave HD, Poder L, Kho RM, Burnett
TL, Khan Z, King C, Shen L, Colak C, Burk KS, Andrieu PIC,
Franco IVP, Glanc P, Kielar AZ, Taffel MT, Kania LM, Bonde
A, Pectasides M, Arif-Tiwari H, Laifer-Narin S, Nicola R, Jha P
(2024) Radiology State of the art Review: Endometriosis Imaging
Interpretation and Reporting. Radiology 312:e233482. h t t p s : / / d o i
. o r g / 1 0 . 1 1 4 8 / r a d i o l . 2 3 3 4 8 2
24. Rousset P, Florin M, Bharwani N, Touboul C, Monroc M, Gol -
fier F, Nougaret S, Thomassin-Naggara I; ENDOV ALIRM Group
(2023) Deep pelvic infiltrating endometriosis: MRI consensus
lexicon and compartment-based approach from the ENDO -
V ALIRM group. Diagn Interv Imaging 104:95–112. h t t p s : / / d o i .
o r g / 1 0 . 1 0 1 6 / j . d i i i . 2 0 2 2 . 0 9 . 0 0 4
25. Pitot MA, Bookwalter CA, Dudiak KM (2020) Mullerian duct
anomalies coincident with endometriosis: a review. Abdom
Radiol (NY) 45:1723–1740. h t t p s : / / d o i . o r g / 1 0 . 1 0 0 7 / s 0 0 2 6 1 - 0 2
0 - 0 2 4 6 5 - y
26. Vercellini P, Salmeri N, Somigliana E, Piccini M, Caprara F,
Viganò P, De Matteis S (2024) Mullerian anomalies and endo -
metriosis as a potential explanatory models for the retrograde
menstruation/implantation and the embryonic remnants/celomic
Authors and Affiliations
Brooke S. Lampl1 · Cara R. King2 · Marjan Attaran2 · Myra K. Feldman1
Brooke S. Lampl
[email protected]
Myra K. Feldman
[email protected]
Cara R. King
[email protected]
Marjan Attaran
[email protected]
1 Imaging Institute, Cleveland Clinic, Cleveland, United States
2 Ob/Gyn and Women’s Health Institute, Cleveland Clinic,
Cleveland, United States
1 3
4853