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IMAGING SPECTRUM OF BENIGN UTERINE DISEASE
AND TREATMENT OPTIONS
Penyaji : dr.Apriansah Nara Sumber : dr.TitikYuliastuti, Sp.Rad(K)
Stephanie Nougaret, MD, PhD, Martina Sbarra, MD, Jessica Robbins, MD. © 2019 Elsevier Inc
INTRODUCTION
Benign uterine diseases
(Adenomyosis, leiomyomas)
are common gynecologic
conditions affecting women
of all ages
USG : first-line imaging
technique
MRI : the most accurate
tool in lesion diagnosis
and patient management
Discusses typical and
atypical MRI findings
of adenomyosis and
leiomyomas and
therapeutic options
MAGNETIC RESONANCE IMAGING PROTOCOL
Patient Preparation
 Fasting and use antiperistaltic agent (Hyoscine Butylpromide
or glucagon)
 A moderately full bladder
IMAGING PROTOCOL
High-resolution thin-section images acquired at 1.5 T or 3.0 T are recommended.
T2WI location of the lesion relative to the endometrial cavity
T1WI (with/without FS) presence of fat or blood contents and can be used to detect the
presence of lymph nodes and bone marrow abnormalities
Large-FOVT1WI/T2WI secondary signs of pelvic mass effect, such as hydronephrosis,
and malignant disease, such as lymph nodes or peritoneal
carcinomatosis
Contrast-enhanced T1WI FS characterization, vascularization, and its differentiation from an
adnexal mass
Dynamic contrast injection/
MR angiography
uterine artery anatomy and collateral gonadal arterial supply
DWI characterization and distinction between leiomyoma and
leiomyosarcoma
LEIOMYOMAS
EPIDEMIOLOGY, PATHOPHYSIOLOGY
 The most common, 20%-30% of reproductive-aged women
 Unknown cause composed of multiple layers of smooth muscle
fascicles and fibrous connective tissue anchored in the muscular
wall of the uterus
 Solitary or, most frequently, multiple
 May be asymptomatic, 20%-50% with menorrhagia,
dysmenorrhea, urinary frequency, pelvic and back pain, and
dyspareunia
LOCATION
Leiomyoma FIGO classification system according to location. The leiomyoma FIGO
classification: 0, pedunculated intracavitary; 1, submucosal less than 50% intramural; 2,
submucosal greater than or equal to 50% intramural; 3, contacts endometrium, 100% intramural;
4, intramural; 5, subserosal greater than or equal to 50% intramural; 6, subserosal less than 50%
intramural; 7, subserosal pedunculated; 8, other (specify; eg, cervical, parasitic)
Unusual locations
diffuse peritoneal
leiomyomatosis
multiple lesions along the
peritoneal surfaces
iatrogenic dissemination
Intravenous
leiomyomatosis
aggressive intravascular growth
pattern within intrauterine and
systemic veins
benign metastasizing
leiomyoma
IMAGING FEATURES
Ultrasonography
 Well-defined mass, often shadowing at the margin and/or producing
internal linear shadowing.
 Varies from hypoechoic to hyperechoic in relation to the
myometrium.
 Dystrophic calcifications can be seen particularly in postmenopausal
women.
 On color Doppler US, circumferential blood flow around the lesion is
often seen
Magnetic resonance imaging
 Sensitivities and specificities of 94.1% and 68.7%, respectively, for uterine leiomyomas
Isointense signal intensity on T1-weighted image (C), and homogeneous contrast enhancement
(F). The blackout phenomenon is shown, with no signs of restricted diffusion with low signal
intensity on DW image (b = 1000) (D) and corresponding ADC map (E).
Myometrial lesion with
endometrial contact (arrows) in
keeping with a FIGO 3
leiomyoma. Nondegenerated
leiomyoma appears as a well-
defined lesion with hypointense
signal intensity on T2-weighted
images related to the outer
myometrium (A,B)
SagittalT2 AxialT2 AxialT1
Axial DWI ADC AxialT1 FS Contrast
Nondegenerated
leiomyoma
SagittalT2 AxialT2
A well-delineated lesion (arrow)
of intermediate to high signal
intensity without T2 dark areas
(A, B). Isointense lesion without
hemorrhage (C, arrow). (D)
DWI (b = 1000) shows high
signal intensity (arrow) with
restriction on (E) corresponding
map (arrow). (F) avid and
heterogeneous enhancement
without necrosis (arrow).
Axial obliqueT1
Axial DWI ADC Axial obliqueT1 FS C
The absence of hemorrhage and necrosis, T2 dark signal, and
the presence of well-defined border favor a cellular leiomyoma
rather than leiomyosarcoma; this was confirmed histologically.
Cellular
leiomyoma
Different types of leiomyoma degeneration
Hyaline degeneration
(A) Axial T2-weighted image and (B) contrast-enhanced axial T1-weighted
fat-saturated image show a leiomyoma (arrow) with hypointense signal
intensity on T2-weighted image and poor enhancement after gadolinium
injection, suggesting hyaline degeneration.
T2 WI T1-WI FS+C
CYSTIC DEGENERATION
(C) Axial T2-weighted image and (D) sagittal T2-weighted image showa
large,well-defined cystic lesion (arrow) with high T2 signal intensity,
consistent with cystic leiomyoma because of its uterine origin (claw sign).
MYXOID DEGENERATION
(E) Sagittal T2-weighted fat-
saturated image and (F) contrast-
enhanced sagittal T1-weighted fat-
saturated image show a
leiomyoma (arrow) presenting
areas with high signal intensity on
T2-weighted image and
enhancement after gadolinium
injection, with the exception of the
nonenhancing mucinous lakes,
suggesting a myxoid leiomyoma
HEMORRHAGIC DEGENERATION
(G) Axial T1-weighted fat-
saturated image and (H)
axial T2 FS show a left
parauterine lesion (white
arrow) with a component
of very high signal
intensity on T1-weighted
image and low signal
intensity on T2-weighted
image, suggesting
intralesional hemorrhage.
The lesion is a hemorrhagic subserosal pedunculated leiomyoma
(MR imaging FIGO 7) with enlarged and tortuous vessel (black
arrow, H) that extends from the uterus to the mass (bridging
vessel sign), indicating the uterine origin of the lesion.
PITFALLSTO AVOID ON MAGNETIC RESONANCE IMAGING
1. Distinction between an ovarian mass and a uterine mass
Axial T2-weighted image shows a well-
defined Left parauterine mass with low
signal intensity that could resemble
either a uterine leiomyoma or ovarian
fibroma.
In this case, the left ovary (black arrow)
is normal and separate fromthemass.
Enlarged and tortuous vessels
extended from the uterus to supply the
mass (white arrows, bridging vessels
sign), suggesting the diagnosis of
uterine leiomyoma.
2. FOCAL MYOMETRIAL CONTRACTIONS
(A) Sagittal and (B) axial T2-W FS
images. Axial T2-WI shows
hypointense bands perpendicular
to the junctional zone (JZ) in the
anterior myometrium (arrows, B).
This finding was absent on
previous sagittal T2-weighted
image that shows normal uterus
with thin and distinct JZ (arrow, A),
confirming the diagnosis of
transient myometrial contraction.
3. ENDOMETRIAL POLYP
 Submucosal leiomyoma may be mistaken for an endometrial polyp
 Polyps have heterogeneous or high signal onT2WI, in contrast with
pedunculated submucosal leiomyomas, which are low signal onT2WI and
have a stalk that arises from the myometrium
4.ADENOMYOMAS
Discussed later
5. LEIOMYOSARCOMAS
Axial T2-weighted image shows dark T2
area (arrow, A) and ill-defined border.
Hemorrhage is seen on the axial T1-
weighted image (arrow, B). (C) Axial
oblique DW image (b = 1000) shows
high signal intensity (arrow). (D)
Contrast-enhanced axial oblique T1-
weighted fat-saturated image shows
heterogeneous enhancement with
central necrosis (arrow).
These combined features are
suggestive of leiomyosarcoma, which
was confirmed histologically.
AxialT2 AxialT1
Axial DWI AxialT1 FS + C
The role of MR imaging in differentiating leiomyoma and uterine sarcoma
TREATMENT OPTIONS
▪ Asymptomatic leiomyomas do not require treatment
▪ Oral contraceptives or gonadotropin-releasing hormone (GnRH) agonists
may be used to reduce menstrual bleeding associated with leiomyomas, may
also reduce the size of leiomyomas.
▪ Women with refractory abnormal bleeding or those experiencing bulk
symptoms, such as pelvic fullness, constipation, or urinary symptoms, may
be eligible for surgical management :
▪ Uterine sparing myomectomy : 3 or fewer dominant symptomatic
leiomyomas less than 8 cm in diameter
▪ Hysteroscopic myomectomy : submucosal leiomyomas predominantly
intracavitary, less than 4 cm in size, and have at least 5 mm of intact
myometrium overlying the leiomyoma
 UAE is a minimally invasive uterine-sparing treatment option for
leiomyomas resulting in abnormal bleeding, anemia, and/or bulk
symptoms.
 UAE is an alternative to myomectomy, but, unlike myomectomy, it is also
useful in patients with multiple (>3) and large (>10 cm) leiomyomas.
 UAE offers the opportunity to preserve fertility, improves or eliminates
bulk symptoms and bleeding, is durable, and has a low complication rate.
 There is a roughly 10% to 15% treatment failure rate in which patients
require additional treatment with hysterectomy, myomectomy, or repeat
UAE.
ADENOMYOSIS
Epidemiology, Clinical Symptoms, and Pathophysiology
• Ectopic endometrial glands and stroma in the myometrium more than 2.5
mm from the endometrium-myometrium interface
• 1/3 are asymptomatic, symptoms nonspecific : dysmenorrhea, menorrhagia,
and abnormal vaginal bleeding
• Associated with female infertility, overlapping pathophysiology and
association with endometriosis
• Cause of adenomyosis is still unclear : exposure to estrogen, prior uterine
surgery, and parity are known risk factors
ULTRASONOGRAPHY IMAGING FEATURES
 Myometrial heterogeneity with thin linear shadowing (venetian blinds)
alternating with increased echogenicity, globular uterine enlargement,
asymmetric thickening of the myometrium (pseudowidening sign), and
isolated or clustered small anechoic cysts
 May be similar to uterine leiomyoma
 Leiomyomas : usually have a well-defined border and peripheral color flow
 Adenomyomas : illdefined, show less mass effect, and have diffuse and
central color flow
MAGNETIC RESONANCE IMAGING FEATURES
Sensitivity of 46.1%, specificity of 99.2%, and positive predictive value of 92.3%
(A) Classic features of
adenomyosis: subendometrial
cysts and diffuse thickening
(orange arrow) of the JZ.
(B) enlarged uterus with the
classic MRI appearance of
adenomyosis as thickening of the
JZ, particularly of the anterior
myometrium (orange arrow) with
multiple foci with high T2 signal
(white arrows).
(C) (D) Show a high-T2 and high-
T1 focus within the anterior
myometrium (arrow, C, D) caused
by hemorrhagic content.
SagittalT2
AxialT2 AxialT1
SUBTYPES OF ADENOMYOSIS
(A) The different : adenomyoma and
leioemyoma. An adenomyoma is T2
dark with internal bright foci caused by
endometrial glands, whereas a typical
leiomyoma is homogeneously dark
with a bright peripheral rim caused by
perilesional edema that generally
causes more adjacent mass effect than
adenomyoma.
(B) Show an ill-defined, low-signal
intensity mass with embedded
hyperintense foci in the posterior
myometrium (arrow, B) suggesting an
adenomyoma.
1.Adenomyoma
SagittalT2
(C) a well-defined, low-signal-intensity mass with embedded hyperintense foci bulging into the
endometrium (arrow, C) suggesting a subendometrial adenomyoma.
(D) an enlarged uterus, with the coexistence of an adenomyoma, as ill-defined hypointense
masslike lesion with embedded hyperintense punctate foci in the posterior myometrium (white
arrow), and a leiomyoma as well defined very hypointense mass in the anterior myometrium
causing adjacent mass effect (black arrow)
Axial obliqueT2-WI SagittalT2-WI
2. HEMORRHAGIC CYSTIC ADENOMYOSIS
(A) Diffuse thickening of the JZ
and a single intramural focus of
high signal intensity in the
anterior myometrium (arrow).
(B, C) The cystlike focus is
better seen on (B) and (C),
characterized by T1 and T2 high
signal (arrow, B, C), confirming
hemorrhagic content.
SagittalT2 FS AxialT1-WI
AxialT2 WI
• External adenomyosis : outer part of the uterus, most likely in the
posterior myometrium, disrupting the serosa but not affecting the JZ,
usually associated with deep endometriosis. On MR imaging, it appears as
an ill-defined subserosal posterior T2-hypointense mass/pseudomass and
may containT2-hyperintense small cystic areas.
• Adenomyomatous polyp or polypoid adenomyoma : polypoid mass in the
lower uterine endometrium or endocervix, and accounts for about 2% of
all endometrial polyps. On MR imaging, it is a hypointense polypoid mass
associated withT2- hyperintense foci.
MAGNETIC RESONANCE IMAGING DIFFERENTIAL DIAGNOSIS
1. Cyclic physiologic changes of the uterus (pseudothickening of the JZ):
hormone dependent and changes according to the menstrual cycle. not
be performed during menstruation
2. Nonmeasurable JZ: postmenopausal patients and in women using
contraceptive drugs.
3. Myometrial contractions
4. Endometrial cancer : adenomyosis can be seen in 20% of patients with
endometrial cancer. DWI may help to define the depth of myometrial
invasion; adenomyosis does not restrict diffusion, whereas endometrial
cancer does (Fig. 13)
5. Leiomyoma : traditionally, adenomyomas present as a T2 hypointense
mass with ill-defined borders, minimal mass effect, and with multiple bright
foci. In contrast, leiomyoma, besides also being T2 hypointense, also has a
well-defined border, adjacent mass effect, and large vessels surrounding the
lesion (see Fig. 10)
Pseudowidening of the JZ with coexisting
endometrial cancer. (A) The pseudowidening
of the JZ. Sagittal (B) and (C) show an
intermediate T2 signal within the endometrial
cavity (orange arrow) with diffuse thickening
of the JZ bulging in the endometrial cavity
(pseudowidening of the JZ, black arrow). Note
the large cystic area on (B, D) consistent with a
subendometrial cyst (white arrow). On (D)
signal hyperintensity is solely seen at the level
of the intermediate T2 signal corresponding
with the endometrial cancer (orange arrow).
No areas of restricted diffusion are seen
within the pseudowidening of the JZ. In this
case, DWI was particularly helpful to delineate
the cancer.
axial obliqueT2-WI
Sagital obliqueT2-
WI
FuseT2-DWI
TREATMENT OPTIONS
 Medical therapy for adenomyosis relies on hormonal suppression.
 Levonorgestrel-releasing IUDs may be slightly more efficacious than oral
contraceptives in reducing pain and uterine bleeding and seem to improve
quality-of-life measures similarly or slightly more than hysterectomy.
 Traditionally, the standard treatment of symptomatic adenomyosis has
been hysterectomy
 Complete adenomyomectomy is effective in the setting of a focal
adenomyoma.
 Partial adenomyomectomy, removal of a portion of the clinically
recognizable adenomyosis, is used in the setting of diffuse adenomyosis
when complete resection would effectively result in a functional
hysterectomy.
 In select patients, UAE can be used to treat adenomyosis with or without
leiomyomas.
SUMMARY
 Benign uterine diseases, including adenomyosis and leiomyomas, are
common conditions affecting women of all ages.
 US is often the initial imaging study obtained; however, MR imaging
is the preferred modality for additional lesion characterization and
provides critical information to assist in selecting the appropriate
therapies for symptomatic patients.
 Treatment options for adenomyosis and leiomyomas include
medical, surgical, and minimally invasive techniques such as UAE.
dr. Apri PPT (Jurnal) Imaging Spectrum Of Benign Uterine Disease And Treatment Options.pdf

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dr. Apri PPT (Jurnal) Imaging Spectrum Of Benign Uterine Disease And Treatment Options.pdf

  • 1. IMAGING SPECTRUM OF BENIGN UTERINE DISEASE AND TREATMENT OPTIONS Penyaji : dr.Apriansah Nara Sumber : dr.TitikYuliastuti, Sp.Rad(K) Stephanie Nougaret, MD, PhD, Martina Sbarra, MD, Jessica Robbins, MD. © 2019 Elsevier Inc
  • 2. INTRODUCTION Benign uterine diseases (Adenomyosis, leiomyomas) are common gynecologic conditions affecting women of all ages USG : first-line imaging technique MRI : the most accurate tool in lesion diagnosis and patient management Discusses typical and atypical MRI findings of adenomyosis and leiomyomas and therapeutic options
  • 3. MAGNETIC RESONANCE IMAGING PROTOCOL Patient Preparation  Fasting and use antiperistaltic agent (Hyoscine Butylpromide or glucagon)  A moderately full bladder
  • 4. IMAGING PROTOCOL High-resolution thin-section images acquired at 1.5 T or 3.0 T are recommended. T2WI location of the lesion relative to the endometrial cavity T1WI (with/without FS) presence of fat or blood contents and can be used to detect the presence of lymph nodes and bone marrow abnormalities Large-FOVT1WI/T2WI secondary signs of pelvic mass effect, such as hydronephrosis, and malignant disease, such as lymph nodes or peritoneal carcinomatosis Contrast-enhanced T1WI FS characterization, vascularization, and its differentiation from an adnexal mass Dynamic contrast injection/ MR angiography uterine artery anatomy and collateral gonadal arterial supply DWI characterization and distinction between leiomyoma and leiomyosarcoma
  • 5. LEIOMYOMAS EPIDEMIOLOGY, PATHOPHYSIOLOGY  The most common, 20%-30% of reproductive-aged women  Unknown cause composed of multiple layers of smooth muscle fascicles and fibrous connective tissue anchored in the muscular wall of the uterus  Solitary or, most frequently, multiple  May be asymptomatic, 20%-50% with menorrhagia, dysmenorrhea, urinary frequency, pelvic and back pain, and dyspareunia
  • 6. LOCATION Leiomyoma FIGO classification system according to location. The leiomyoma FIGO classification: 0, pedunculated intracavitary; 1, submucosal less than 50% intramural; 2, submucosal greater than or equal to 50% intramural; 3, contacts endometrium, 100% intramural; 4, intramural; 5, subserosal greater than or equal to 50% intramural; 6, subserosal less than 50% intramural; 7, subserosal pedunculated; 8, other (specify; eg, cervical, parasitic)
  • 7. Unusual locations diffuse peritoneal leiomyomatosis multiple lesions along the peritoneal surfaces iatrogenic dissemination Intravenous leiomyomatosis aggressive intravascular growth pattern within intrauterine and systemic veins benign metastasizing leiomyoma
  • 8. IMAGING FEATURES Ultrasonography  Well-defined mass, often shadowing at the margin and/or producing internal linear shadowing.  Varies from hypoechoic to hyperechoic in relation to the myometrium.  Dystrophic calcifications can be seen particularly in postmenopausal women.  On color Doppler US, circumferential blood flow around the lesion is often seen
  • 9. Magnetic resonance imaging  Sensitivities and specificities of 94.1% and 68.7%, respectively, for uterine leiomyomas
  • 10. Isointense signal intensity on T1-weighted image (C), and homogeneous contrast enhancement (F). The blackout phenomenon is shown, with no signs of restricted diffusion with low signal intensity on DW image (b = 1000) (D) and corresponding ADC map (E). Myometrial lesion with endometrial contact (arrows) in keeping with a FIGO 3 leiomyoma. Nondegenerated leiomyoma appears as a well- defined lesion with hypointense signal intensity on T2-weighted images related to the outer myometrium (A,B) SagittalT2 AxialT2 AxialT1 Axial DWI ADC AxialT1 FS Contrast Nondegenerated leiomyoma
  • 11. SagittalT2 AxialT2 A well-delineated lesion (arrow) of intermediate to high signal intensity without T2 dark areas (A, B). Isointense lesion without hemorrhage (C, arrow). (D) DWI (b = 1000) shows high signal intensity (arrow) with restriction on (E) corresponding map (arrow). (F) avid and heterogeneous enhancement without necrosis (arrow). Axial obliqueT1 Axial DWI ADC Axial obliqueT1 FS C The absence of hemorrhage and necrosis, T2 dark signal, and the presence of well-defined border favor a cellular leiomyoma rather than leiomyosarcoma; this was confirmed histologically. Cellular leiomyoma
  • 12. Different types of leiomyoma degeneration Hyaline degeneration (A) Axial T2-weighted image and (B) contrast-enhanced axial T1-weighted fat-saturated image show a leiomyoma (arrow) with hypointense signal intensity on T2-weighted image and poor enhancement after gadolinium injection, suggesting hyaline degeneration. T2 WI T1-WI FS+C
  • 13. CYSTIC DEGENERATION (C) Axial T2-weighted image and (D) sagittal T2-weighted image showa large,well-defined cystic lesion (arrow) with high T2 signal intensity, consistent with cystic leiomyoma because of its uterine origin (claw sign).
  • 14. MYXOID DEGENERATION (E) Sagittal T2-weighted fat- saturated image and (F) contrast- enhanced sagittal T1-weighted fat- saturated image show a leiomyoma (arrow) presenting areas with high signal intensity on T2-weighted image and enhancement after gadolinium injection, with the exception of the nonenhancing mucinous lakes, suggesting a myxoid leiomyoma
  • 15. HEMORRHAGIC DEGENERATION (G) Axial T1-weighted fat- saturated image and (H) axial T2 FS show a left parauterine lesion (white arrow) with a component of very high signal intensity on T1-weighted image and low signal intensity on T2-weighted image, suggesting intralesional hemorrhage. The lesion is a hemorrhagic subserosal pedunculated leiomyoma (MR imaging FIGO 7) with enlarged and tortuous vessel (black arrow, H) that extends from the uterus to the mass (bridging vessel sign), indicating the uterine origin of the lesion.
  • 16. PITFALLSTO AVOID ON MAGNETIC RESONANCE IMAGING 1. Distinction between an ovarian mass and a uterine mass Axial T2-weighted image shows a well- defined Left parauterine mass with low signal intensity that could resemble either a uterine leiomyoma or ovarian fibroma. In this case, the left ovary (black arrow) is normal and separate fromthemass. Enlarged and tortuous vessels extended from the uterus to supply the mass (white arrows, bridging vessels sign), suggesting the diagnosis of uterine leiomyoma.
  • 17. 2. FOCAL MYOMETRIAL CONTRACTIONS (A) Sagittal and (B) axial T2-W FS images. Axial T2-WI shows hypointense bands perpendicular to the junctional zone (JZ) in the anterior myometrium (arrows, B). This finding was absent on previous sagittal T2-weighted image that shows normal uterus with thin and distinct JZ (arrow, A), confirming the diagnosis of transient myometrial contraction.
  • 18. 3. ENDOMETRIAL POLYP  Submucosal leiomyoma may be mistaken for an endometrial polyp  Polyps have heterogeneous or high signal onT2WI, in contrast with pedunculated submucosal leiomyomas, which are low signal onT2WI and have a stalk that arises from the myometrium
  • 20. 5. LEIOMYOSARCOMAS Axial T2-weighted image shows dark T2 area (arrow, A) and ill-defined border. Hemorrhage is seen on the axial T1- weighted image (arrow, B). (C) Axial oblique DW image (b = 1000) shows high signal intensity (arrow). (D) Contrast-enhanced axial oblique T1- weighted fat-saturated image shows heterogeneous enhancement with central necrosis (arrow). These combined features are suggestive of leiomyosarcoma, which was confirmed histologically. AxialT2 AxialT1 Axial DWI AxialT1 FS + C
  • 21. The role of MR imaging in differentiating leiomyoma and uterine sarcoma
  • 22. TREATMENT OPTIONS ▪ Asymptomatic leiomyomas do not require treatment ▪ Oral contraceptives or gonadotropin-releasing hormone (GnRH) agonists may be used to reduce menstrual bleeding associated with leiomyomas, may also reduce the size of leiomyomas.
  • 23. ▪ Women with refractory abnormal bleeding or those experiencing bulk symptoms, such as pelvic fullness, constipation, or urinary symptoms, may be eligible for surgical management : ▪ Uterine sparing myomectomy : 3 or fewer dominant symptomatic leiomyomas less than 8 cm in diameter ▪ Hysteroscopic myomectomy : submucosal leiomyomas predominantly intracavitary, less than 4 cm in size, and have at least 5 mm of intact myometrium overlying the leiomyoma
  • 24.  UAE is a minimally invasive uterine-sparing treatment option for leiomyomas resulting in abnormal bleeding, anemia, and/or bulk symptoms.  UAE is an alternative to myomectomy, but, unlike myomectomy, it is also useful in patients with multiple (>3) and large (>10 cm) leiomyomas.  UAE offers the opportunity to preserve fertility, improves or eliminates bulk symptoms and bleeding, is durable, and has a low complication rate.  There is a roughly 10% to 15% treatment failure rate in which patients require additional treatment with hysterectomy, myomectomy, or repeat UAE.
  • 25. ADENOMYOSIS Epidemiology, Clinical Symptoms, and Pathophysiology • Ectopic endometrial glands and stroma in the myometrium more than 2.5 mm from the endometrium-myometrium interface • 1/3 are asymptomatic, symptoms nonspecific : dysmenorrhea, menorrhagia, and abnormal vaginal bleeding • Associated with female infertility, overlapping pathophysiology and association with endometriosis • Cause of adenomyosis is still unclear : exposure to estrogen, prior uterine surgery, and parity are known risk factors
  • 26. ULTRASONOGRAPHY IMAGING FEATURES  Myometrial heterogeneity with thin linear shadowing (venetian blinds) alternating with increased echogenicity, globular uterine enlargement, asymmetric thickening of the myometrium (pseudowidening sign), and isolated or clustered small anechoic cysts  May be similar to uterine leiomyoma  Leiomyomas : usually have a well-defined border and peripheral color flow  Adenomyomas : illdefined, show less mass effect, and have diffuse and central color flow
  • 27. MAGNETIC RESONANCE IMAGING FEATURES Sensitivity of 46.1%, specificity of 99.2%, and positive predictive value of 92.3% (A) Classic features of adenomyosis: subendometrial cysts and diffuse thickening (orange arrow) of the JZ. (B) enlarged uterus with the classic MRI appearance of adenomyosis as thickening of the JZ, particularly of the anterior myometrium (orange arrow) with multiple foci with high T2 signal (white arrows). (C) (D) Show a high-T2 and high- T1 focus within the anterior myometrium (arrow, C, D) caused by hemorrhagic content. SagittalT2 AxialT2 AxialT1
  • 28. SUBTYPES OF ADENOMYOSIS (A) The different : adenomyoma and leioemyoma. An adenomyoma is T2 dark with internal bright foci caused by endometrial glands, whereas a typical leiomyoma is homogeneously dark with a bright peripheral rim caused by perilesional edema that generally causes more adjacent mass effect than adenomyoma. (B) Show an ill-defined, low-signal intensity mass with embedded hyperintense foci in the posterior myometrium (arrow, B) suggesting an adenomyoma. 1.Adenomyoma SagittalT2
  • 29. (C) a well-defined, low-signal-intensity mass with embedded hyperintense foci bulging into the endometrium (arrow, C) suggesting a subendometrial adenomyoma. (D) an enlarged uterus, with the coexistence of an adenomyoma, as ill-defined hypointense masslike lesion with embedded hyperintense punctate foci in the posterior myometrium (white arrow), and a leiomyoma as well defined very hypointense mass in the anterior myometrium causing adjacent mass effect (black arrow) Axial obliqueT2-WI SagittalT2-WI
  • 30. 2. HEMORRHAGIC CYSTIC ADENOMYOSIS (A) Diffuse thickening of the JZ and a single intramural focus of high signal intensity in the anterior myometrium (arrow). (B, C) The cystlike focus is better seen on (B) and (C), characterized by T1 and T2 high signal (arrow, B, C), confirming hemorrhagic content. SagittalT2 FS AxialT1-WI AxialT2 WI
  • 31. • External adenomyosis : outer part of the uterus, most likely in the posterior myometrium, disrupting the serosa but not affecting the JZ, usually associated with deep endometriosis. On MR imaging, it appears as an ill-defined subserosal posterior T2-hypointense mass/pseudomass and may containT2-hyperintense small cystic areas. • Adenomyomatous polyp or polypoid adenomyoma : polypoid mass in the lower uterine endometrium or endocervix, and accounts for about 2% of all endometrial polyps. On MR imaging, it is a hypointense polypoid mass associated withT2- hyperintense foci.
  • 32. MAGNETIC RESONANCE IMAGING DIFFERENTIAL DIAGNOSIS 1. Cyclic physiologic changes of the uterus (pseudothickening of the JZ): hormone dependent and changes according to the menstrual cycle. not be performed during menstruation 2. Nonmeasurable JZ: postmenopausal patients and in women using contraceptive drugs. 3. Myometrial contractions
  • 33. 4. Endometrial cancer : adenomyosis can be seen in 20% of patients with endometrial cancer. DWI may help to define the depth of myometrial invasion; adenomyosis does not restrict diffusion, whereas endometrial cancer does (Fig. 13) 5. Leiomyoma : traditionally, adenomyomas present as a T2 hypointense mass with ill-defined borders, minimal mass effect, and with multiple bright foci. In contrast, leiomyoma, besides also being T2 hypointense, also has a well-defined border, adjacent mass effect, and large vessels surrounding the lesion (see Fig. 10)
  • 34. Pseudowidening of the JZ with coexisting endometrial cancer. (A) The pseudowidening of the JZ. Sagittal (B) and (C) show an intermediate T2 signal within the endometrial cavity (orange arrow) with diffuse thickening of the JZ bulging in the endometrial cavity (pseudowidening of the JZ, black arrow). Note the large cystic area on (B, D) consistent with a subendometrial cyst (white arrow). On (D) signal hyperintensity is solely seen at the level of the intermediate T2 signal corresponding with the endometrial cancer (orange arrow). No areas of restricted diffusion are seen within the pseudowidening of the JZ. In this case, DWI was particularly helpful to delineate the cancer. axial obliqueT2-WI Sagital obliqueT2- WI FuseT2-DWI
  • 35. TREATMENT OPTIONS  Medical therapy for adenomyosis relies on hormonal suppression.  Levonorgestrel-releasing IUDs may be slightly more efficacious than oral contraceptives in reducing pain and uterine bleeding and seem to improve quality-of-life measures similarly or slightly more than hysterectomy.  Traditionally, the standard treatment of symptomatic adenomyosis has been hysterectomy
  • 36.  Complete adenomyomectomy is effective in the setting of a focal adenomyoma.  Partial adenomyomectomy, removal of a portion of the clinically recognizable adenomyosis, is used in the setting of diffuse adenomyosis when complete resection would effectively result in a functional hysterectomy.  In select patients, UAE can be used to treat adenomyosis with or without leiomyomas.
  • 37. SUMMARY  Benign uterine diseases, including adenomyosis and leiomyomas, are common conditions affecting women of all ages.  US is often the initial imaging study obtained; however, MR imaging is the preferred modality for additional lesion characterization and provides critical information to assist in selecting the appropriate therapies for symptomatic patients.  Treatment options for adenomyosis and leiomyomas include medical, surgical, and minimally invasive techniques such as UAE.