Dwi
DWI is a functional MRI technique, performed without contrast administration,
that provides information about the intracellular, transcellular, and
extracellular Brownian motion of water molecules in a tissue (true diffusion),
as well as the microcirculation (perfusion), which can be evaluated
separately ( 1 ) . In tissues with increased cellularity and a
resultant increase in cell membrane surface area, there is a decrease in
Brownian motion (i.e., restricted diffusion), whereas there is an increase in
Brownian motion (i.e., free diffusion) in tissues with decreased cellularity.
The ADC, which represents a combination of true diffusion and perfusion, is a
numerical value assigned to the degree of such motion in a tissue and has been
used as a marker of cellularity.
Free diffusion, qualitatively visible as progressive signal loss on DWI obtained
with increasing b values and quantitatively measured as a region with a high
ADC, can be seen in tissues with low cellularity ( 4 ) . In contrast,
restricted diffusion, qualitatively visible as high signal intensity on DWI
obtained with increasing b values and quantitatively measured as a region with a
low ADC, is associated with hypercellularity and has been used as an indicator
of potential malignancy ( 4 ) .
In DWI, the b values represent different diffusion-sensitizing gradient strengths
and are expressed as s/mm 2 (time/area). Because the ADC is the slope
of exponential decrease in signal intensities between DWI sequences with
different b values, DWI with ADC mapping is performed with at least two
different b values. At lower b values, the perfusion-related contribution is
higher, which can affect the ADC, and the image mirrors a heavily T2W
fat-suppressed sequence. The predominant contributor changes from perfusion to
diffusion at b values in the 100-300 s/mm 2
range ( 1 ) . At higher b values (> 1000
s/mm 2 ), there can be a progressive decrease in the signal-to-noise
ratio ( 5 ) .
The ADC is expressed as a numerical value × 10 −3
mm 2 /s and represents a quantitative metric. It quantifies the
progressive loss of signal in a tissue of interest visible on DWI performed with
successively increasing b values. A region of interest can be drawn by the
radiologist in the tissue of interest to obtain a numeric
value ( 4 ) . The region of interest results in automatically
generated ADCs, presented as minimum, mean, and maximum values or as a mean
value.
In pelvic examinations, DWI is most commonly acquired in the axial plane.
However, obtaining sequences with the same orientation as that of T2W images
allows fusion imaging and optimizes anatomic correlation ( 6 ) .
One should bear in mind some pitfalls when interpreting DWI sequences. In
general, high-cellularity tumors demonstrate restricted diffusion, whereas
normal tissue does not. However, benign tissue components, such as blood, fat,
necrosis and pus, may also show restricted diffusion ( 6 ) . As a result, DWI
characteristics of benign and malignant tumors, including those of the ovary,
may overlap ( 7 ) . It is crucial to correlate DWI and ADC data
with morphological characteristics to minimize the probability of
misinterpretation.
It is also important to keep in mind the fact that DWI is based on T2W images,
causing tissues with long T2 relaxation time, such as simple cysts, to show high
signal intensity-the so-called T2-shine-through effect. However, an ovarian mass
with a hypointense signal on DWI, the ADC map, and T2W images-the so-called
T2-blackout effect-is most likely a benign mass ( 2 ) , making DWI
particularly suited to excluding the possibility of malignancy.
The
The ovaries are usually ovoid in shape and average 10 cm 3 in
volume ( 8 ) . The zonal anatomy is best appreciated on T2W
images, the normal medulla showing increased signal intensity relative to the
cortex, reflecting the greater amount of loosely packed stroma and blood
vessels, and diminished cellularity of the medulla ( 8 ) . In women of
reproductive age, there are multiple follicles in the cortex, appearing as
thin-walled cystic structures, the fluid content of which results in high signal
intensity on T2W images and low signal intensity on T1W
images ( 8 ) . On T2W images, the corpus luteum demonstrates
wall thickening, with low to intermediate signal intensity, that corresponds to
a layer of luteinized theca cells ( 8 ) .
In women of reproductive age, the normal ovary may have high enough signal
intensity to be identified on DWI sequences from zero to high b values,
especially during the luteal phase. Ovarian follicles may show high signal
intensity on all DWI sequences (even at high b values), with concomitant high
ADCs ( 9 ) .
Mature cystic teratomas are the most common ovarian tumors in women under 45
years of age ( 10 ) . They are composed of mature tissue from at
least two of the three germ cell layers (endoderm, mesoderm, and ectoderm);
in 88% of cases, they are filled with sebaceous material, which is liquid at
body temperature, and are lined with keratinized squamous
epithelium ( 11 ) . They grow slowly, at an average rate of
1.8 mm each year, prompting some researchers to advocate nonsurgical
management of smaller (< 6 cm) tumors ( 12 ) . In 10% of
cases, the tumors are bilateral ( 13 ) . Mature cystic teratomas
contain hair follicles, skin glands, muscle, and other tissues. There is
usually a raised protuberance projecting into the cyst cavity, known as a
Rokitansky nodule ( 13 ) . Ectodermal tissue (skin and neural
derivatives) is invariably present, as are mesodermal tissue (fat, bone,
cartilage, and muscle) in over 90% of cases and endodermal tissue (e.g.,
gastrointestinal epithelium, bronchial epithelium, and thyroid tissue) in
most cases ( 13 ) . Although it is one of the most relevant
features, adipose tissue is present in only 67-75% of
cases ( 13 ) .
Mature cystic teratomas have typical imaging features on MRI ( Table 1 ). Their adipose content
displays a signal that is hyperintense on T1W images and becomes hypointense
after selective fat saturation. This characteristic is sufficient to
establish the diagnosis of a ovarian teratoma ( 13 ) .
Findings in benign ovarian lesions with restricted diffusion.
With hemorrhagic infarction. FS, fat saturation.
It has been suggested that the abnormal signal intensity displayed on DWI by
most mature cystic teratomas is caused by the presence of keratin, a protein
originating from the cytoskeletal structure of the
epidermis ( 7 ) . Other sites showing abnormal signal
intensity include Rokitansky nodules and fat globules ( 7 ) . The restricted
Brownian movement of water molecules within the keratinous substance results
in a high signal intensity on DWI and low ADCs ( Figure 1 ). In fact, DWI can facilitate the diagnosis of
mature cystic teratomas, especially those containing a small amount of fat
that is not detectable by conventional MRI ( 14 , 15 ) .
Figure 1 MRI of a 32-year-old female patient with a left mature cystic
teratoma. A: Axial T1W image showing a cystic
lesion with areas of high signal intensity in which the signal
became hypointense after fat saturation (not represented).
B: Axial DWI at b = 1000 s/mm 2 ,
showing areas of high signal intensity within the lesion.
C: ADC map showing low ADCs within the
lesion.
MRI of a 32-year-old female patient with a left mature cystic
teratoma. A: Axial T1W image showing a cystic
lesion with areas of high signal intensity in which the signal
became hypointense after fat saturation (not represented).
B: Axial DWI at b = 1000 s/mm 2 ,
showing areas of high signal intensity within the lesion.
C: ADC map showing low ADCs within the
lesion.
Mature cystic teratomas undergo malignant transformation in 1-2% of the
cases ( 13 ) . Malignant transformation tends to occur in
older women (between 60 and 70 years of age), squamous cell carcinoma being
the most common histological type. In such cases, they can show restricted
diffusion in their solid component, due to
hypercellularity ( 10 ) . The morphological correlation is
mandatory, because malignant mural nodules tend to show intermediate signal
intensity on T2W images and enhancement after gadolinium
administration ( 15 ) .
When an ovarian follicle enlarges during the menstrual cycle but does not
rupture for ovulation, a follicular cyst, typically measuring between 3 cm
and 6 cm, may develop. In some cases, these cysts undergo hemorrhage,
becoming hemorrhagic cysts. On MRI, a hemorrhagic cyst usually has high
signal intensity on T1W images and intermediate to high signal intensity on
T2W images ( Table 1 ). There is smooth
enhancement on the cyst wall, without vegetations or
nodularity ( 6 ) . Because of their blood content, hemorrhagic
cysts may display restricted diffusion ( 6 ) .
Endometriomas, also known as endometriotic cysts, are benign cysts that
constitute an ovarian manifestation of endometriosis. On MRI, endometriomas
typically appear as cystic lesions, typically multiple or bilateral, with
thick walls ( 16 ) . They show high signal intensity on T1W
images, with or without selective fat suppression, and relatively low signal
intensity on T2W images-the shading sign ( 17 ) . However, this
sign is not exclusive to endometriomas, given the fact that T2 shading can
also be observed in hemorrhagic cysts and other benign or malignant
non-endometrioid adnexal tumors ( 18 ) , leading to diagnostic
difficulties.
Because endometriomas contain blood and some hemosiderin, they show T1
shortening, high signal intensity on DWI, and lower
ADCs ( 7 ) , as depicted in Figure 2 . The presence of restricted diffusion in
endometriomas may hamper the detection of malignant transformation, making
the correlation with other sequences mandatory. Solid nodules showing
intermediate signal intensity on T2W images, peritoneal metastases,
thickened septa (> 3 mm), or contrast enhancement are likely to be
malignant ( 19 ) . Clear cell and endometrioid carcinomas are
the most common malignant tumors associated with endometriomas.
Figure 2 MRI of a 41-year-old female patient with endometriomas.
A: Axial T1W image with fat suppression,
showing bilateral cystic lesions with high signal intensity.
B: Axial DWI at b = 1000 s/mm 2 ,
showing areas of high signal intensity within the lesions.
C: ADC map showing low ADCs within the
lesions.
MRI of a 41-year-old female patient with endometriomas.
A: Axial T1W image with fat suppression,
showing bilateral cystic lesions with high signal intensity.
B: Axial DWI at b = 1000 s/mm 2 ,
showing areas of high signal intensity within the lesions.
C: ADC map showing low ADCs within the
lesions.
DWI and ADC mapping may play roles in differentiating between hemorrhagic
cysts and endometrioma. In a recent study, including 24 benign cystic
hemorrhagic adnexal lesions, Balaban et al. ( 20 ) reported that
ADCs were significantly lower in endometriomas than in hemorrhagic cysts, a
fact that can be used to differentiate between the two conditions. There
are, however, more reliable ways of making this distinction, in particular
the presence of the T2 dark spot sign, which has high specificity for
chronic hemorrhage ( 16 ) .
Ovarian torsion usually presents as acute severe pelvic pain and is caused by
partial or complete rotation of the ovarian vascular pedicle. Predisposing
factors include an underlying ovarian tumor (especially one > 6 cm),
hypermobile adnexa, and elongated fallopian tubes ( 21 ) . Ovarian
torsion most commonly affects women under 30 years of
age ( 21 ) .
In cases of ovarian torsion, venous blood flow is initially compromised,
causing edema and swelling. Later, the dual arterial blood supply is also
compromised, leading to hemorrhagic infarction ( 22 ) , which in turn
results in irreversible loss of the ovary.
The most common characteristics of the lesion in adults are an enlarged ovary
with areas of signal hyperintensity on T1W and T2W images ( Table 1 ), due to hemorrhage and edema,
respectively. Peripheral follicles can also be
observed ( 23 ) . In the late phases, gangrenous necrosis
develops.
To date, there have been no studies demonstrating that the use of DWI adds
value in the diagnosis of ovarian torsion. However, DWI has been shown to be
beneficial in identifying hemorrhagic infarction ( 24 ) : low ADCs are
more common in torsed ovaries with hemorrhagic infarction than in those
without.
In the majority of cases, tubo-ovarian abscesses result from pelvic
inflammatory disease, being more common in women of reproductive
age ( 25 ) . Tubo-ovarian abscesses are thick-walled,
multilocular adnexal masses. They may contain septa, pus, gas, or fluid,
with or without fluid-debris levels ( 25 ) . The content usually displays
a heterogeneously intermediate signal on T2W images ( Table 1 ). Areas of necrosis or loculated fluid
collections may resemble serous fluid but can also be proteinaceous or
hemorrhagic with T1 shortening ( 26 ) . Tubo-ovarian abscesses are
surrounded by thick, markedly enhancing outer borders.
Tubo-ovarian abscesses comprise viscous proteinaceous fluid containing
bacteria, inflammatory cells, cellular debris, and necrotic tissue. When the
content is more viscous, the signal intensity is higher on DWI and lower on
the ADC map ( 27 ) , as shown in Figure 3 . Depending on the viscosity of the pus, the abscess
contents may show heterogeneous restricted diffusion. Chronic abscesses,
abscesses smaller than 1 cm in diameter, and abscesses in patients on
antibiotic therapy may not show restricted diffusion ( 28 ) .
Figure 3 MRI of a 39-year-old female patient with a left tubo-ovarian
abscess. A: Axial T2W image showing a cystic lesion
with heterogeneous high-signalintensity content. B:
Axial DWI at b = 1000 s/mm 2 , showing areas of high
signal intensity within the lesion. C: ADC map
showing low ADCs within the lesion.
MRI of a 39-year-old female patient with a left tubo-ovarian
abscess. A: Axial T2W image showing a cystic lesion
with heterogeneous high-signalintensity content. B:
Axial DWI at b = 1000 s/mm 2 , showing areas of high
signal intensity within the lesion. C: ADC map
showing low ADCs within the lesion.
DWI also plays a role in making a distinction between tubo-ovarian abscesses
and cystic or necrotic neoplasms. Neoplasms typically show restricted
diffusion at the periphery, where the cell density is higher, whereas
abscesses show central restricted diffusion ( 24 ) .
Fibromas are the most common solid ovarian tumors and account for 4% of all
ovarian neoplasms ( 29 ) . Fibromas are benign tumors that can
present at any age, although the mean age of occurrence is in the late
forties. Fibromas that are highly cellular are classified as either cellular
fibromas or fibrosarcomas. Cellular fibromas constitute 10% of all ovarian
fibromas and have low malignant potential, whereas fibrosarcomas are
malignant tumors ( 29 , 30 ) .
On MRI, fibromas usually present low signal intensity on T1W images, low
signal intensity on T2W images, and weak, delayed enhancement after contrast
administration. In the majority of these tumors, T2-shortening effects,
caused by the abundant collagen contents and the decreased extracellular
fluid, result in a signal decrease on T2W images ( 31 ) . The pathology
examination can reveal edema and cystic degeneration, which explain the
varying degree of intermediate to high signal intensity portions on T2W
images, which may mimic malignancy, in some cases ( 32 ) .
Thecomas account for 0.5-1.0% of all primary ovarian tumors and are most
likely to occur in postmenopausal women ( 29 ) . In most
cases, they exhibit estrogenic activity ( 33 ) . With rare
exceptions, they are considered benign neoplasms ( 29 ) .
On MRI, when compared with predominantly fibrous tumors, pure thecomas tend
to exhibit higher signal intensity on T2W images and more avid contrast
enhancement, a major pitfall in the diagnosis of malignant ovarian tumors of
the ovary ( 30 ) . The accurate diagnosis of these tumors and
their differentiation from malignant tumors is critical for correct patient
management. DWI, in combination with ADC mapping, may play a role in making
that distinction. According to the most recent European Society of
Urogenital Radiology guidelines for indeterminate adnexal masses, a solid
lesion that exhibits low signal intensity on T2W images and on DWI with high
b values is highly likely to be benign ( 2 , 34 ) . However, isolated ADC
measurements in the solid component have not been found to contribute to
differentiating between benign and malignant adnexal masses, possibly due to
the lower mean ADCs in benign fibrous tumors associated with dense fibrous
stromal proliferation. In such tumors, no signal increase is observed on
DWI, despite their low ADCs, probably as a consequence of the T2 blackout
effect ( 2 ) . Nevertheless, some fibromas and thecomas in
this group may show restricted diffusion. For instance, functioning thecomas
and cellular fibromas may show high signal intensity on DWI and relatively
low ADCs ( Figure 4 ), due to their
relatively high cellularity ( 35 - 37 ) .
Figure 4 MRI of a 67-year-old female patient with thecoma. A:
Axial T2W image showing a solid lesion with intermediate signal
intensity. B: Axial DWI at b = 1000
s/mm 2 , showing high signal intensity within the
lesion. C: ADC map showing low ADCs within the
lesion.
MRI of a 67-year-old female patient with thecoma. A:
Axial T2W image showing a solid lesion with intermediate signal
intensity. B: Axial DWI at b = 1000
s/mm 2 , showing high signal intensity within the
lesion. C: ADC map showing low ADCs within the
lesion.
Intro
In ovarian disorders, conventional morphological evaluation in T1-weighted (T1W) and
T2-weighted (T2W) magnetic resonance imaging (MRI) sequences is essential. However,
diffusion-weighted imaging (DWI) has undeniable diagnostic value, providing
excellent tissue contrast based on the molecular diffusion of
water ( 1 ) . This fact is particularly relevant in
differentiating between benign and malignant ovarian tumors ( 2 ) . In general, the latter
show restricted diffusion, whereas the former do not. Nevertheless, there are some
exceptions. The restricted diffusion of water molecules is proportional to the
following: expansion of the intracellular compartment, as in cytotoxic edema;
increased cell membrane density due to hypercellularity; increased fluid viscosity;
and increased tortuosity of the extracellular space ( 3 ) . In fact, restricted
diffusion may be observed in normal tissue, in solid non-malignant lesions with high
cellular density, or in cystic non-malignant lesions with high
viscosity ( 3 ) . To avoid diagnostic pitfalls, DWI should always be
evaluated in conjunction with the apparent diffusion coefficient (ADC) maps and
correlated with conventional anatomic MRI scans (T1W and T2W sequences).
Conclusions
In ovarian disorders, conventional morphological evaluation with T1W and T2W images
is essential. However, DWI has experienced a rise in popularity, due to its
undeniable diagnostic value, particularly in differentiating between benign and
malignant tumors. It is advisable to use DWI as a complementary sequence, whenever
possible, because it can provide excellent tissue contrast based on the molecular
diffusion of water within tumors. As a general rule, malignant tumors present
restricted diffusion, whereas benign tumors do not. Nevertheless, radiologists
should be aware of some lesions that constitute exceptions to that rule: teratomas,
endometriomas, hemorrhagic cysts, ovarian abscesses, ovarian infarction, and some
benign sex cord-stromal tumors.