Skip to main content
Sage Choice logoLink to Sage Choice
. 2021 May 26;43(5):239–252. doi: 10.1177/01617346211017462

Contrast-Enhanced Ultrasound Imaging of Uterine Disorders: A Systematic Review

Barbara Stoelinga 1,, Lynda Juffermans 1, Anniek Dooper 1, Marleen de Lange 2, Wouter Hehenkamp 2, Thierry Van den Bosch 3, Judith Huirne 4
PMCID: PMC8299780  PMID: 34036872

Abstract

Uterine disorders are often presented with overlapping symptoms. The microvasculature holds specific information important for diagnosing uterine disorders. Conventional sonography is an established diagnostic technique in gynecology, but is limited by its inability to image the microvasculature. Contrast-enhanced ultrasound (CEUS), is capable of imaging the microvasculature by means of intravascular contrast agents; that is, gas-filled microbubbles. We provide a literature overview on the use of CEUS in diagnosing myometrial and endometrial disorders, that is, fibroids, adenomyosis, leiomyosarcomas and endometrial carcinomas, as well as for monitoring and enhancing the effectiveness of minimally invasive therapies. A systematic literature search with quality assessment was performed until December 2020. In total 34 studies were included, published between 2007 and 2020.The results entail a description of contrast-enhancement patterns obtained from healthy tissue and from malignant and benign tissue; providing a first base for potential diagnostic differentiation in gynecology. In addition it is also possible to determine the degree of myometrial invasion in case of endometrial carcinoma using CEUS. The effectiveness of minimally invasive therapies for uterine disorders can safely and accurately be assessed with CEUS. In conclusion, the abovementioned applications of CEUS are promising and it is worth further exploring its full potential for gynecology by designing innovative and methodologically high-quality clinical studies.

Keywords: contrast-enhanced ultrasound, imaging, microvasculature, uterine disorders, systematic review

Introduction

Uterine disorders are often presented with overlapping symptoms. Some disorders, such as fibroids, are usually correctly identified by conventional grayscale or Doppler imaging. Other disorders such as diffuse adenomyosis and malignant leiomyosarcomas are often difficult to distinguish from common fibroids. The microvascular architecture and blood flow patterns of uterine disorders can provide detailed information important for accurate differentiation. However, detection of vessels smaller than 0.1 mm in diameter and full quantification of vascular flow remain beyond the reach of conventional grayscale and Doppler imaging techniques. 1

Contrast-enhanced ultrasound (CEUS), not to be confused with saline- or gel-infused sonohysterography, is an imaging technique capable of visualizing both macro- and microvasculature by means of intravenously injected gas-filled microbubbles. 2 A schematic overview for performing CEUS in gynecological setting is depicted in Figure 1. Microbubbles oscillate in the ultrasound beam, thereby reflecting a unique, non-linear echo that stands in contrast to the linear echo produced by the surrounding tissue. This non-linear echo, containing harmonics of the transmitted frequency, can be converted into a contrast-enhanced image that displays tissue vascularization, as microbubbles remain intravascular. 3

Figure 1.

Figure 1.

Schematic representation of performing contrast-enhanced ultrasonography (CEUS) in gynecological setting. Step 1: intravenous injection of, for example, SonoVue ultrasound contrast agent. Injection is regulary done via a catheter and 5 mL of saline is flushed after the diluted sonovue is injected (a). Ultrasound contrast agents (microbubbles) remain intravascular (b). Step 2: transvaginal (or abdominal) ultrasound scan of the uterus (c). Providing a contrast-enhanced image of the uterus (d), showing hyper-enhancement of the myometrium (M) compared with the endometrium (E). Step 3: the CEUS image can be fully quantified, providing a time-intensity curve (e) from which parameters such as wash-in rate (1), peak intensity (2), and wash-out rate (3) can be obtained.

Another important advantage of CEUS is the possibility of full quantification of the signal. Quantification of the contrast-enhanced signal is mostly established by analyzing the tissue-specific parameters, such as wash-in phase, peak intensity and wash-out phase, which are converted into a time-intensity curve (Figure 1(e)). The wash-in phase starts from the first arrival of contrast, usually 20 to 30 seconds after intravenous injection, during this period the level of intensity increases progressively until it reaches a plateau (peak intensity). This is followed by the wash-out phase during which the signal disappears or falls into noise level. Research often focusses on finding one parameter or a combination of parameters that is specific for discrimination for example malignant from benign tissue.

In general, the microvasculature of benign tumor tissue is different from malignant tumor tissue. Malignant lesions show enhanced tumor-induced angiogenesis, that is, sprouting of new blood vessels enabling tumor growth. These new tumor vessels are generally disorganized and leaky, often with incomplete vessel wall musculature and larger diameter resulting in low resistance to flow.4,5 Imaging the microvasculature of uterine abnormalities with CEUS may allow for differentiation between benign and malignant uterine disorders.

Besides using CEUS for diagnosing uterine disorders, it can be applied to monitor efficacy of minimally invasive treatments, such as ablation (high-intensity focused ultrasound (HIFU) or microwave ablation) or vascular occlusion (uterine artery embolization). The success rate of minimally invasive treatments, such as ablation or vascular occlusion, relies on the reduction of blood flow. The degree of success can be monitored by the degree of shrinkage or improvement of symptoms. However, there is a delay between treatment and observing shrinkage and/or reduction of symptoms. CEUS could be of prognostic value here, as there is a strong correlation between the degree of vascularity of a fibroid and the success rate of vascular occlusion. 6 For ablation therapy the opposite applies, higher vascularity predicts poor ablation efficacy. 7

CEUS is already an established clinical technique for assessing liver lesions,3,8 renal carcinoma,9,10 and in cardiac imaging, 11 but its value is still to be demonstrated in assessing gynecological disorders. The high potential of CEUS in gynecology was mentioned already in 1997 by Abramowicz. 12 . In 2005 he wrote “Ultrasonographic contrast media: has the time come in obstetrics and gynecology.” 13 Another decade later Pop et al. 14 posed the application of CEUS for diagnosing endometrial pathologies, but concluded that more prospective studies are needed to reach an established role for CEUS in gynecology. The use of CEUS in gynecology was added to the latest update (2018) of the European Federation of Societies for Ultrasound in Medicine and Biology (EFSUMB) guidelines for CEUS in non-hepatic applications, 15 illustrating the novelty of CEUS in this field.

This systematic review provides a literature overview on the potential use of CEUS in diagnosing myometrial and endometrial disorders, differentiating benign and malignant lesions, as well as for monitoring and enhancing effectiveness of minimally invasive therapies. A description of contrast-enhancement characteristics of different types of tissue is reported, dependent on the description provided in the included literature.

Materials and Methods

This systematic review was conducted in accordance with PRISMA (Preferred Reporting Items for Systematic Review and Meta-Analyses) guidelines. In December 2020 one author (BS) performed the search with assistance of a medical science librarian of the Amsterdam UMC in PubMed, Embase, and Cochrane computerized bibliographic databases for eligible studies on patients with myometrial and endometrial disorders (fibroids, adenomyosis, uterine polyps, endometrial cancer, and leiomyosarcoma) who underwent a CEUS for diagnostic purpose or for monitoring minimal invasive therapy. The details of the search strategy are presented in Supplemental Appendix A. Cohort studies, case-control studies, and systematic reviews, published as full paper in English peer-reviewed journals were eligible for inclusion. Studies with less than 10 patients, letters and conference abstracts were excluded, as well as pre-clinical studies about CEUS in animals or laboratory models. Studies reporting on CEUS in diagnosing uterine pathology had to use a reference test. Studies reporting on monitoring effectiveness of minimally invasive therapies were also included when using MRI or conventional US besides CEUS, but without a reference test such as histology. The primary outcome was CEUS characteristics, including enhancement pattern, blood supply, and quantification of perfusion parameters.

After removal of duplicates, two authors (BS and AD) independently screened titles and abstracts to select articles meeting the eligibility criteria. Full texts of the remaining papers were assessed, discrepancies were resolved by discussion. The following data was extracted by BS and AD independently: study design, number of patients, study period, target condition, reference test and outcome measurements.

The risk of bias and methodological quality of the selected studies was assessed (BS and AD) using the quality assessment of diagnostic accuracy studies (QUADAS)-2 tool. 16 Disagreement was resolved by discussion with a third researcher (JH). The QUADAS tool consists of four key domains: patient selection: describing how the patient population was selected; index test: describing how the test was conducted; reference standard: describing how the reference standard was conducted and flow/timing: describing the flow of patient inclusion and exclusion and the interval between the index test and reference standard. The four domains are assessed for risk of bias and rated as a low, high or unclear risk. The first three domains are also assessed for applicability concerns (does the study match the review question?).

When available, data on diagnostic accuracy, sensitivity, specificity, negative predictive value (NPV), positive predictive value (PPV), interclass correlation coefficient (ICC) was extracted or re-calculated by the authors of this review. Although the EFSUMB provided guidelines on how to describe enhancement characteristics in a consistent manner, 15 this is not consistently applied by the cited manuscripts. Enhancement characteristics and quantitative parameters are therefore reported in this review as described in the cited article.

Results

Literature Identification

Searching PubMed, EMBASE, and Cochrane yielded 2323 records (Figure 2). After removing duplicates, title and abstract of 1649 records were screened, resulting in 47 articles. After full-text assessment another 13 articles were excluded. Finally, a total of 34 articles from four countries were included (26 from China). All studies were published between 2007 and 2021. Methodological quality assessment showed a limited number of methodological high-quality studies (Table 1), indicating that results and conclusions should be interpreted with care, keeping bias in mind.

Figure 2.

Figure 2.

Flow chart of literature search on articles reporting on CEUS for diagnosis of uterine disorder, monitoring, and/or enhancing of minimally invasive therapy.

Table 1.

Studies included in review according to the Quality Assessment of Diagnostic Accuracy Studies-2 (QUADAS-2).

Risk of BIAS Applicability concerns
Patient selection Index test Reference standard Flow and timing Patient selection Index test Reference standard
Diagnosis by CEUS
Liu et al. 17 H L L H L L L
Zhang et al. 5 H L H H L L L
Song et al. 18 H H L H L L L
Lieng et al. 19 L L H H L L L
Liu et al. 20 H L L L L L L
Zhou et al. 21 H L L L L L L
Liu et al. 22 L L L L L L L
Su et al. 23 H L L L L L L
Zhang et al. 24 H L L L L L L
Green and Epstein 25 H L L L L L L
Li et al. 26 H L H H L L L
CEUS monitoring effectiveness of therapies
Dorenberg et al. 27 L L H L L L L
Zhou et al. 28 H H H L L L L
Sconfienza et al. 29 H H L H L L L
Wang et al. 30 L H NA L L L NA
Wang et al. 31 H L NA H L L NA
Wang et al. 32 H H NA H L L NA
Lei et al. 33 H L H L L L L
Henri et al. 34 L L H L L L L
Wang et al. 35 L H H L L L L
Xia et al. 36 L L NA L L L NA
Yu et al. 37 L L L H L L L
Zhang et al. 38 L L L H L L L
Wang et al. 39 H L L L L L L
Xu et al. 40 H L L L L L L
CEUS-Enhancing effectiveness HIFU
Peng et al. 41 H H L H L L L
Dorenberg et al. 42 H H H L L L L
Cheng et al. 43 L L L L L L L
Isern et al. 44 L L H H L L L
Jiang et al. 45 H L H L L L L
Orsi et al. 46 L L L L L L L
Peng et al. 47 H L H H L L L
Chen et al. 55 L L L L L L L
Jingqi et al. 48 L L L H L L L

L = low risk; H = high risk; NA = not applicable; CEUS = contrast-enhanced ultrasound; HIFU = high-intensity focused ultrasound.

Contrast Ultrasound Enhancement Characteristics and Quantification

Contrast-enhancement characteristics of normal uterine tissue and uterine disorders are described below and summarized in Table 2. Diagnostic accuracy, sensitivity, and specificity, NPV and PPV are shown in Table 3, if available for the cited studies.

Table 2.

Contrast-enhanced ultrasound enhancement characteristics.

Normal uterus Enhancement order: uterine artery and outer myometrial layer, inner myometrial layer, and endometrial layer; clear boundary endometrium and myometrium
Fibroids ≥2 cm Initial perfusion pseudocapsule; homo- or heterogeneous enhancement entire lesion; well demarcated border between pseudocapsule and myometrium
Fibroids <2 cm No early enhancement pseudocapsule; iso-enhancement; late phase: wash-out lesion faster than myometrium
Adenomyosis Heterogeneous enhancement of affected myometrium
Leiomyosarcoma Earlier enhancement feeding vessels of lesion than those of the myometrium; heterogeneous hyper-enhancement; no enhancement in center
Endometrial carcinoma Enhancement of lesions with greater intensity than normal myometrium, with irregular, tortuous blood vessels. Wash-in and wash-out faster than normal myometrium

Table 3.

Diagnostic accuracy of contrast-enhanced ultrasound (CEUS) with histology as reference test.

Author Study design Diagnosis Number of patients Histology Sensitivity Specificity Diagnostic accuracy (%) NPV PPV Remark
Zhang et al. 5 Prospective cohort study Fibroids 165 Fibroids Yes NA NA 97 NA NA Nine fibroids with sarcomatous change
Song et al. 18 Prospective cohort study Endometrial carcinoma 35 EC Yes 0.66 0.83 79 0.83 0.64 Averaged for disease stages 1a,b,c
Lieng et al. 19 Prospective cohort Endometrial carcinoma 17 EC Yes 0.80 0.69 NR NR NR
Polyps 17 Polyps
Liu et al. 20 Prospective cohort study Endometrial carcinoma 35 EC Yes 0.86 0.85 83 NA NA
Liu et al. 17 Case-control Endometrial carcinoma 79 EC Yes 0.82 0.73 85 0.96 0.60
40 Control
Zhou et al. 21 Prospective cohort study Endometrial carcinoma 68 Suspect EC (26 EC) Yes 0.77 0.74 75 0.83 0.65 2D CEUS
0.85 0.83 84 0.90 0.76 2D + 3D CEUS
Liu et al. 22 Prospective cohort study Endometrial carcinoma 49 EC Yes 0.92 0.88 83 NA NA Sensitivity and specificity for “peak intensity
42 Benign lesions
Su et al. 23 Prospective cohort study Endometrial carcinoma 39 EC Yes NA NA 83 NA NA Diagnostic accuracy for myometrial invasion
42 Hyperplasia
Zhang et al. 24 Retrospective cohort study Endometrial carcinoma 223 EC Yes 0.67 0.77 NA NA NA Predictive value of “enhancement rate” for overall survival
Green et al. 25 Prospective cohort study Endometrial carcinoma 93 EC Yes 0.74 0.87 82 0.87 0.75 Values for myometrial invasion
279 Control
Li et al. 26 Prospective cohort study Fibroid/leiomyosarcoma 143 Fibroids Yes NA NA NA NA NA
4 Sarcomas

Normal endometrium and myometrium

Contrast-enhancement characteristics of a normal uterus (n = 40) was described in one study (Liu et al. 17 ).

During wash in, the uterine artery and outer myometrial layer were first enhanced followed by the inner myometrial layer and subsequently the endometrial layer. The significantly lower peak intensity of the endometrium provided a clear boundary between endometrium and myometrium. During wash-out, contrast agents subsided faster from myometrium than from endometrium. 17

Figure 3 illustrates CEUS of a normal uterus. 49

Figure 3.

Figure 3.

Normal uterus.

Source. Adapted from Stoelinga et al. 49 CEUS scan uterus: conventional gray-scale ultrasound image on the right and CEUS image on the left. CEUS image obtained 14 seconds after contrast injection shows initial enhancement of the (normal) myometrium.

Uterine disorders

Uterine fibroids are the most common benign tumors during the reproductive age. Although the vast majority of fibroids are well recognized by conventional ultrasound, establishing contrast-enhancement characteristics of fibroids may help discriminating other uterine disorders, such as adenomyosis and leiomyosarcomas, from fibroids. Distinctive for fibroids is the highly vascularized peripheral rim, called “pseudocapsule,” from which vessels penetrate into the center of the fibroid. Three studies described CEUS enhancement characteristics of fibroids (n = 348 fibroids.5,26,34). Fibroids enhanced earlier than the surrounding myometrium and the peak intensity differs between the two depending on the degree of fibroid degeneration. A difference was noticed between small and large fibroids, in the study of Zhang e al. 5 with regard to enhancement of the pseudocapsule and the rest of the fibroid. Larger fibroids (>2 cm) first exhibited peripheral enhancement, followed by homogenous or heterogeneous enhancement of the entire lesion. The pseudocapsules of larger fibroids were enhanced slightly stronger than the surrounding myometrium, which resulted in a clearly demarcated border. The pseudocapsule of small fibroids (<2 cm) could not be detected in the early phase. Small fibroids exhibited synchronized iso-enhancement compared with surrounding myometrium. Most fibroids (94,5%) displayed faster wash-out of contrast than the myometrium. 30 One study (Zhang et al. 5 ) examined the diagnostic accuracy of CEUS in diagnosing fibroids compared with conventional ultrasound. Histopathology was performed as reference test on specimen obtained from operation or sonographically-guided percutaneous biopsy. This study, although of low methodological quality with a high risk of bias in patient selection, demonstrated in 96 women a diagnostic accuracy for CEUS of 97.5% for intramural fibroids and 96.3% for other types, such as submucous, subserous and cervical fibroids. Diagnostic accuracy of conventional ultrasound was significantly lower: 85.5% for intramural fibroids (p < .05) and 79.3% for other types of fibroids (p < .01).

Figure 4 illustrates CEUS of a subserosal fibroid. 49

Figure 4.

Figure 4.

Subserosal fibroid (image made at our own institution). On the left CEUS image obtained 19 seconds after contrast injection, shows peripheral enhancement without enhancement in the central part of the fibroid. On the right conventional gray-scale ultrasound image of the same fibroid.

Aside pathology, currently accurate diagnostic tools for leiomyosarcomas are lacking as there are no specific symptoms discriminating malignant leiomyosarcomas from benign (atypical) fibroids. Although a leiomyosarcoma is rare, it is highly aggressive and contributes to a significant proportion of uterine cancer deaths.4,50 Given the aggressiveness of the disease, the risk of tumor cell dissemination in case of inadvertent morcellation50,51 and the lack of reliable diagnostic criteria, there is a need for an imaging technique able to detect this malignancy. Two studies evaluated women with different types of fibroids, including leiomyosarcomas.5,26 Zhang et al. 5 evaluated 96 women with fibroids (also discussed under “uterine fibroids”) and leiomyosarcomas using CEUS and conventional ultrasound, with histology (after surgery or biopsy) as reference test. Li et al. 26 performed CEUS in 147 patients pre-operatively, with post-operative histology as reference test. The contrast-enhancement pattern was similar for all leiomyosarcomas (n = 9 and 4, in studies by Zhang et al. 5 and Li et al. 26 respectively). Sarcomatous lesions showed a heterogeneous hyper-enhancement due to increased blood flow, whereas fibroids (n = 156 and 143 respectively) showed homogeneous enhancement. 5 Seventeen fibroids showed signs of degeneration, of which eight benign and nine malignant. The benign fibroids showed no contrast perfusion in the degenerated area while other parts of the tumors showed the same perfusion as non-degenerated fibroids. The margin of sarcomatous lesions was poorly defined, while fibroids could be well demarcated. Feeding vessels of sarcomatous lesions enhanced earlier than those of the myometrium. By this feature, CEUS was able to detect all nine sarcomas, while conventional US was able to detect only two. 5 Neither studies reported on perfusion parameters or diagnostic accuracy, possibly due to the low number of leiomyosarcomas, yet a diagnostic accuracy of 97% for leiomyosarcoma can be deduced for the study of Zhang et al., 5 but not for the study by Li et al. 26

Adenomyosis is characterized by benign growth of endometrial tissue into the myometrium. The diagnosis is often missed due to its diffuse character30,52 which often requires an additional MRI scan. 53 A recent systematic review described changes in microvasculature of adenomyotic tissue in comparison with normal myometrium due to increased angiogenesis. 54 Therefore, CEUS could theoretically be used to diagnose adenomyosis, however, no studies are yet published on this topic. To date four studies performed CEUS in women who underwent a minimally invasive treatment (HIFU and microwave ablation) of adenomyosis.30,37,40,48 The contrast-enhancement characteristics before ablation were shortly described by Xu et al. 40 as “synchronous enhancement of the entire lesion” (45 cases) and “slow filling from the periphery to the center of the lesion” (21 lesions).

Endometrial carcinoma is the most common gynecological malignancy. 18 This is reflected in the higher number of studies evaluating CEUS for this malignancy: one case-control 17 and seven prospective cohort studies,18,20 -25 with histology-proven endometrial carcinoma. These studies did show different enhancement patterns between malignant and healthy tissue. The principal findings were that enhancement of malignant lesions was in general earlier and with greater intensity than that of normal myometrium and endometrium.17,18,20,21,25 Compared with surrounding tissue, contrast-enhancement was first observed in 57% to 82% of the tumors,18,20,25 with most lesions (61%) being hyper-echogenic, 27% was iso-echogenic, and 11% hypo-echogenic. 17 In 77% the feeding vessels of the tumor were enhanced first and then branched into the endometrial cancer. In the other 23% signals were first visualized in the central portion of the tumor. 18 Inhomogeneous enhancement was observed in 66% of the lesions while 34% showed homogeneous enhancement (Table 2). Importantly, it was shown that endometrial carcinoma had significantly lower perfusion time parameters and higher intensity parameters compared with benign endometrial lesions. 22 The diagnostic value of 3D-CEUS was also demonstrated. In benign lesions, 3D-CEUS showed straight blood vessels of regular shapes near the lesion and sparse blood vessel distribution within the lesion. In malignant lesions, 3D-CEUS revealed tortuous, irregular blood vessels, twisted into groups. 21

Contrast enhanced color- and power Doppler was applied in case of polyps (n = 17) and histology proven endometrial cancer The authors demonstrated that after the injection of intravenous contrast the pulsatility index and resistance index were significantly lower in malignant endometrial lesions. 19 This could be of value for discriminating between benign and malignant endometrial pathology.

Determining the degree of myometrial invasion is important for the staging procedure, as this may affect surgical strategies. The average accuracy of CEUS as diagnostic tool for staging endometrial carcinoma is 81%, with an average sensitivity of 0.78 and specificity of 0.81.17,18,20 -25 The numbers of the individual studies are shown in Table 3. The additional value of combined 2D- and 3D-CEUS imaging (diagnostic accuracy 84%) over 2D-CEUS alone (diagnostic accuracy 75%) was demonstrated in 68 patients with clinically suspected endometrial carcinoma, of which 26 cases were confirmed by histology. 21 Finally, the perfusion parameter “enhancement rate” (dB/s) determined pre-operatively was shown to be an independent predictor for both recurrence of endometrial carcinoma (hazard ratio 1.7; 95% CI 1.0–7.7; p < .05) and overall survival (hazard ratio 2.0; 95% CI 1.0–7.8; p < .05) in a retrospective study with 223 patients. 24

Monitoring and Enhancing Effectiveness of Minimally Invasive Therapies

CEUS for monitoring ablation therapies

The predictive value of quantitative perfusion parameters obtained by CEUS for the therapeutic response to HIFU was assessed by Wang et al. 39 They showed that fibroids with lower perfusion time parameters and higher intensity parameters, that is, “quick-rise-quick-decline” blood flow profile, had poor ablation efficacy. Table 4 provides an overview of the studies using CEUS pre- and post-treatment to image changes in perfusion.

Table 4.

Contrast-enhanced ultrasound (CEUS) for monitoring and enhancing minimally invasive therapy.

Monitoring post-therapy
Reference Treatment Study design N CEUS (pre, per, post) MRI (pre, per, post) Result study/outcome CEUS
Dorenberg et al. 27 UAE fibroids Safety/feasibility 10 Pre Pre Feasibility of CEUS during UAE. Outcome measured with CEUS and compared with MRI: 1 day post-UAE 9/10 pts: MRI = CEUS; 3 months post-UAE 10/10 pts: MRI = CEUS.
Per (directly after UAE) Post (1 day, 3 months)
Zhou et al. 28 HIFU fibroids Prospective cohort study 64 Post (1 week, 1, 3, 6, and 12 months) Post (1 week) Utility of CEUS for early post-HIFU efficacy. Outcome measured with CEUS and MRI; “Got same results with CEUS as with MRI.”
Sconfienza et al. 29 SUFE fibroids Safety/feasibility 12 Pre Post (6 months) Feasibility of CEUS during SUFE. Outcome measured with CEUS and MRI; “CEUS findings similar to dynamic MRI”
Per
Post (1 and 6 months)
Wang et al. 30 HIFU adenomyosis Safety/feasibility 12 Pre Pre Feasibility HIFU of adenomyosis. Outcome measured with CEUS.
Post (1 hour)
Wang et al. 31 Microwave fibroid Prospective cohort study 29 Pre No Accuracy of CEUS in assessing MWA efficacy. Outcome measured with CEUS and conventional US; Pearson r = 0.997.
Per (directly after MWA)
Post (12–24 hours)
Wang et al. 32 HIFU fibroids Safety/feasibility 76 Pre Pre Feasibility USgHIFU of submucosal fibroids. Outcome measured with CEUS and MRI; CEUS vs. CEUS; MRI vs. MRI.
Per (directly after HIFU) Post (1, 3, 5, and 12 months)
Post (1, 3, 6, and 12 months)
Lei et al. 33 Microwave fibroid Prospective cohort study 36; 18 fibroid Post (7 days) Post (7–10 days) Accuracy of CEUS in assessing MWA efficacy. Outcome measured with CEUS and MRI; ICC 0.99.
Wang et al. 35 HIFU fibroids Prospective cohort study 67 Per (directly after HIFU) Post (directly after HIFU; 1, 3, 6, and 12 months) Accuracy of CEUS in assessing HIFU efficacy. Outcome measured with CEUS and MRI; ICC 0.91.
Post (1, 3, 6, and 2 months)
Xia et al. 36 Microwave fibroid Prospective cohort study 88 Per (directly after MWA) Pre Optimized MWA parameters based on MRI before treatment. Outcome measured with CEUS.
Wang et al. 39 HIFU fibroids Retrospective cohort study 263 Pre (directly before HIFU) Pre, Post (1 day) Predictive value of CEUS perfusion parameters on HIFU outcome. Correlation CEUS perfusion parameters pre-HIFU with non-perfused volume ratio post-HIFU.
Per
Henri et al. 34 UAE fibroids Prospective sohort study 40 Pre Pre, Post (6 and 12 months) CEUS is feasible and useful to understand fibroid vascularization and monitoring embolization; its correlation with MRI is good.
Post (directly after AUE, 6 and 12 months)
Yu et al. 37 Microwave adenomyosis Prospective cohort study 278 Per (directly after MWA) Pre Feasibility MWA of adenomyosis. Outcome measured with CEUS and MRI.
Post (3 days)
Zhang et al. 38 Microwave fibroid Prospective cohort study 120; 60 fibroid Pre (1 week) Pre (1 week), Post (6, 12, and 24 months) Accuracy of CEUS in assessing MWA efficacy. Outcome measured with CEUS and MRI; “CEUS is advantageous over MRI.”
Post (6, 12, and 24 months)
Xu et al. 40 Microwave adenomyosis Prospective cohort study 66 Pre Pre Accuracy of CEUS in assessing MWA efficacy. Outcome measured with CEUS and MRI; R = 0.81 for ablation rates
Post (1–2 days) Post (1–2 days)
Enhancing minimal invasive therapy
Dorenberg et al. 42 CEUS-enhanced UAE fibroid Retrospective cohort study 30 Per (directly after UAE) Pre Enhanced UAE by intraprocedural CEUS. Outcome measured with CEUS and MRI.
Post (3 and 12 months)
Peng et al. 41 Intra-procedure CEUS HIFU fibroids Retrospective cohort study 291 Pre Pre Utility of intra-procedural CEUS during HIFU. Outcome measured with CEUS and MRI; “results from CEUS correlated well with results from MRI.”
Per (10 minutes prior to HIFU) Post (1 day)
Post
Jiang et al. 45 CEUS-enhanced HIFU fibroid Randomized controlled trial 80 Per (MB infusion 5 minutes prior to HIFU) Pre Feasibility of CEUS-enhanced HIFU. Outcome measured by MRI.
Post (directly after HIFU) Post (1 day)
Cheng et al. 43 Intra-procedure CEUS HIFU fibroids and adenomyosis Retrospective/safety cohort study 2604 Per (directly after HIFU) Pre Safety of intra-procedural CEUS during HIFU. Outcome measured with CEUS during HIFU and MRI post-therapy.
Post (1 day)
Peng et al. 47 Intra-procedure CEUS HIFU fibroids Prospective cohort study 68 Per (8 minutes prior to HIFU) Pre Utility of intra-procedural CEUS during HIFU. Outcome measured with CEUS and MRI; R = 0.96 for NPV.
Post (directly after HIFU) Post (1 day)
Orsi et al. 46 CEUS-enhanced HIFU fibroid Randomized controlled trial 33 Pre Pre (1 week) Feasibility of CEUS-enhanced HIFU. Outcome measured by MRI.
Per (MB infusion 15 seconds prior to HIFU) Post (1, 3, 6, and 12 months)
Post (directly after HIFU)
Isern et al. 44 CEUS-enhanced HIFU fibroid Retrospective cohort study 319 Per (MB infusion 2 minutes prior to HIFU) Pre Safety of CEUS-enhanced HIFU. Outcome measured by MRI.
Post (directly after HIFU)
Jingqi et al. 48 CEUS-enhanced HIFU adenomyosis Safety study cohort study 102 Per (1 or 10 minutes prior to HIFU) Pre Safety of CEUS-enhanced HIFU. Outcome measured by MRI.
Post (1 day)
Chen et al. 55 CEUS-enhanced HIFU fibroid Prospective cohort study 120 Per (MB infusion 6/10 minutes prior to HIFU) Pre Feasibility of CEUS-enhanced HIFU. Outcome measured by MRI.
Post (directly after HIFU) Post (1 day)

HIFU is a minimally invasive therapy to ablate fibroids and adenomyosis. Three studies described the ability of CEUS to detect non-perfused ablation areas in treated fibroids28,32,35,39 and two studies in adenomyosis.30,48 These studies also performed MRI as reference test, however only one study compared CEUS and MRI data and found an ICC of 0.910 (p < .01). 35 Two retrospective41,43 and one prospective study 47 examined the safety of CEUS as intra-procedural, real-time technique for US-guided HIFU to assess ablation results. Residual CEUS-enhancement was observed in 15% to 35% of the treated lesions and an additional HIFU treatment was then performed in the same session. Apart from monitoring, CEUS can also be used to enhance effectiveness of HIFU when applied just before treatment. It is thought to work via cavitating microbubbles during HIFU exposure, which may mechanically destruct the fibroid and further increase the temperature for ablation therapy. Five studies, one retrospective 44 and four prospective studies45,46,48,55 investigated this enhancing potential of CEUS on HIFU treatment. However, all studies choose different time points of injecting SonoVue, varying from 1 to 10 minutes prior to HIFU treatment. Elimination half-life of SonoVue is approximately 6 minutes, 56 these studies were therefore performed under different blood concentrations of SonoVue. Most important findings of these studies were shorter insonication time required to ablate 1 cm 3 of fibroid to reach massive grayscale changes, and less energy applied in the presence of microbubbles. Results on fibroid shrinkage on the long-term did not differ.

Microwave ablation is similar to HIFU, that is, an ablation technique that aims at heating fibroid tissue. Where HIFU works within diagnostic frequencies (0.6–5.0 MHz), microwave ablation works with electromagnetic waves (900–2450 MHz) and is typically used to ablate larger tumors (>3.0 cm). 57 Four studies demonstrated the use of CEUS for monitoring microwave ablation of fibroids,31,33,36,38 and two studies for monitoring this treatment of adenomyosis.37,40 Quantitative analysis demonstrated good agreement between contrast-enhanced MRI and CEUS for detecting non-perfused volume after microwave ablation of fibroids (ICC = 0.991) 33 and ablation rate in adenomyosis (R = 0.81). 40

CEUS for monitoring uterine artery embolization

Uterine artery embolization (UAE) is a minimally invasive technique injecting embolization particles under angiographic guidance to occlude the uterine artery and thereby blood supply to the fibroid. Three pilot studies demonstrated feasibility of CEUS to image the degree of fibroid perfusion directly after UAE in the angiography room. All three studies showed good agreement between CEUS and MRI results.27,29,34 Successful application of CEUS during UAE was also described in a retrospective study (n = 30). In five cases the endpoint of embolization was adjusted based on findings with CEUS, that is, embolization was continued. 42

Contrast Agents and Adverse Events

In general, adverse reactions to ultrasound contrast agents in humans are rare, usually transient and of mild intensity. The incidence of severe hypersensitivity or anaphylactic reactions is less than 0.002%, which is lower than current X-ray agents and comparable with MR contrast agents. 58 SonoVue was used as contrast agent in all of the included studies. The administered dose ranged from 1.0 to 4.8 mL, the most commonly used dosage was 2.4 mL. No serious adverse events were reported in any of the discussed studies. In the studies where CEUS was used to monitor or enhance effectiveness of minimally invasive therapies common ablation-related side-effects were mentioned, such as discomfort hot skin sensation and pain in treated region. The side-effects were transient and disappeared 1 to 4 hours post-procedure, all pain scores were mild (<4).20,27 -39,41,43 -48,55 The differences in side-effects between “HIFU” and “HIFU + CEUS” are listed in Supplemental Appendix B.

Discussion

Contrast-enhanced ultrasound in gynecology has gained more and more interest over the last two decades. We provided an extensive systematic review to describe CEUS enhancement characteristics for specific myometrial and endometrial disorders that may serve as a basis for potential diagnostic differentiation of uterine fibroids, adenomyosis, leiomyosarcoma, and endometrial carcinoma. Yet conclusive evidence still has to be provided by well-designed clinical trials. This review does demonstrate that CEUS can readily be used to monitor effectiveness of minimally invasive therapies. CEUS may also be used to stimulate the effectiveness of these minimally invasive therapies, however, the added value on the longer term is not yet demonstrated. The safety of this intraprocedural CEUS in terms of side-effects seems not be affected, though this needs to be carefully evaluated in future studies. This was recently also concluded in a review specifically about CEUS for monitoring minimally invasive treatments for uterine fibroids. 59

There are established methods for diagnosing several uterine disorders, and one may question the added value of CEUS for example for fibroids, which are in general well recognized on grayscale ultrasound. Adenomyosis, however, remains a challenging disorder to diagnose based on grayscale ultrasound. Another challenge is the diagnosis of leiomyosarcomas as the clinical presentation of uterine sarcomas is nonspecific and the ultrasound characteristics of grayscale ultrasound resemble those of fibroids. In order to achieve accurate differentiation between different disorders using CEUS it is important to document the contrast-enhancement characteristics of fibroids as well as other pathologies in a structured and standardized manner. Up till now, enhancement characteristics have been described in the researchers sole discretion. This is also reflected in Table 2, and unfortunately this does not provide the necessary diagnostic information when assessing a patients CEUS scan for adenomyosis or a malignancy.

In general, diagnosis of uterine disorders and monitoring effectiveness of minimally invasive therapies can typically be performed using dynamic MRI, as this reference test provides good quality information on morphology, size, and vascularization. In clinical practice, CEUS may be added as second diagnostic imaging technique after the initial grayscale ultrasound and prior to an MRI scan—which typically has long waiting lists—or in medical centers where MRI is not available. 29 In order for CEUS to become a clinically established imaging technique and potentially an alternative for MRI, diagnostic accuracy should be determined not only by histology, but also by quantitative comparison with MRI. Remarkably, none of the studies that used CEUS as a diagnostic tool performed an MRI, all used histology as reference test. Fifteen studies performed MRI as post-treatment imaging modality, of which six studies described that results obtained with both CEUS and MRI were similar27 -29,38,41,45 and four studies made a statistical comparison of CEUS with MRI33,35,40,47 in gynecology. In the characterization of non-gynecology malignancies, for example focal hepatic lesions and recognizing malignancies, there are studies showing a similar-to-higher accuracy of CEUS compared with MRI.60,61 Notably, CEUS has several advantages over MRI: (1) imaging in real-time, allowing continuous assessment of the enhancement period, whereas MRI scans can only be made at distinct time points; (2) ultrasound contrast agents remain intravascular, unlike MRI contrast agents, providing information specifically on vascular flow; (3) high spatial resolution, ability to imaging the microvasculature; (4) the option to apply CEUS in out-patient clinic; (5) lower cost than MRI and CT. 62

Limitations

Despite the high potential of CEUS, the methodological quality of the included studies could not provide conclusive support for current implementation of CEUS in daily gynecological practice. As mentioned before, the role of CEUS has been established in other fields of specialty. This might be taken as “fait accompli” by some groups, who have put CEUS into use in gynecology without the need for setting up a clinical study aimed at establishing the role of CEUS with a consistent report of enhancement characteristics and/or statistical comparison with MRI.

The included studies may represent a selection bias as most studies did not report on inclusion and exclusion criteria and the number of excluded patients. In addition, most studies had small sample sizes and patients were selected based on previous diagnosis of uterine pathology. This could mean that the diagnostic value of CEUS may be overestimated. Additionally, by far most of the referenced studies were conducted in China, a country with a wide use of CEUS in various clinical scenarios.

A note of interest is that we cannot exclude a possible overlap between included patients in some of the papers. Liu et al. 17 included patients with histology-proven endometrial carcinoma between January 2008 and April 2011. Whereas the study by Liu et al. 22 published in 2016 included patients between January 2010 and March 2014. The retrospective study by Peng et al. 47 on intraprocedural CEUS during HIFU may have described the results from a number of the same patients that were included in a prospective study by the same group in 2014. 45

Conclusion

This review demonstrates the limited number of methodological high-quality clinical studies and structural reports on CEUS application in gynecology. CEUS obtained different contrast-enhancement patterns between malignant tissue (leiomyosarcomas and endometrial carcinoma) and healthy or benign tissue (normal myometrium, fibroids or adenomyosis); providing a first base for potential diagnostic differentiation in gynecology. In addition, the results show that it is also possible to determine the degree of myometrial invasion in case of endometrial carcinoma using CEUS. The effectiveness of minimally invasive therapies for uterine disorders can safely and accurately be assessed with CEUS.

In conclusion, CEUS is a promising technique and it is worth further exploring its full potential for gynecology by designing innovative and methodologically high-quality clinical studies.

Footnotes

Declaration of Conflicting Interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding: The author(s) received no financial support for the research, authorship, and/or publication of this article.

ORCID iD: Barbara Stoelinga Inline graphic https://orcid.org/0000-0002-6595-4433

Supplemental Material: Supplemental material for this article is available online.

References

  • 1. Testa AC, Ferrandina G, Fruscella E, Van Holsbeke C, Ferrazzi E, Leone FP, et al. The use of contrasted transvaginal sonography in the diagnosis of gynecologic diseases: a preliminary study. J Ultrasound Med. 2005;24(9):1267-78. [DOI] [PubMed] [Google Scholar]
  • 2. Dijkmans PA, Juffermans LJ, Musters RJ, van Wamel A, ten Cate FJ, van Gilst W, et al. Microbubbles and ultrasound: from diagnosis to therapy. Eur J Echocardiogr. 2004;5(4):245-56. [DOI] [PubMed] [Google Scholar]
  • 3. Brannigan M, Burns PN, Wilson SR. Blood flow patterns in focal liver lesions at microbubble-enhanced US. Radiographics. 2004;24(4):921-35. [DOI] [PubMed] [Google Scholar]
  • 4. Exacoustos C, Romanini ME, Amadio A, Amoroso C, Szabolcs B, Zupi E, et al. Can gray-scale and color Doppler sonography differentiate between uterine leiomyosarcoma and leiomyoma? J Clin Ultrasound. 2007;35(8):449-57. [DOI] [PubMed] [Google Scholar]
  • 5. Zhang XL, Zheng RQ, Yang YB, Huang DM, Song Q, Mao YJ, et al. The use of contrast-enhanced ultrasound in uterine leiomyomas. Chin Med J (Engl). 2010;123(21):3095-9. [PubMed] [Google Scholar]
  • 6. Isonishi S, Coleman RL, Hirama M, Iida Y, Kitai S, Nagase M, et al. Analysis of prognostic factors for patients with leiomyoma treated with uterine arterial embolization. Am J Obstet Gynecol. 2008;198(3):270 e1-6. [DOI] [PubMed] [Google Scholar]
  • 7. Liu J, Keserci B, Yang X, Wei J, Rong R, Zhu Y, et al. Volume transfer constant (K(trans)) maps from dynamic contrast enhanced MRI as potential guidance for MR-guided high intensity focused ultrasound treatment of hypervascular uterine fibroids. Magn Reson Imaging. 2014;32(9):1156-61. [DOI] [PubMed] [Google Scholar]
  • 8. Dietrich CF, Nolsøe CP, Barr RG, Berzigotti A, Burns PN, Cantisani V, et al. Guidelines and good clinical practice recommendations for contrast-enhanced ultrasound (CEUS) in the liver–update 2020 WFUMB in cooperation with EFSUMB, AFSUMB, AIUM, and FLAUS. Ultrasound Med Biol. 2020;46(10):2579-604. [DOI] [PubMed] [Google Scholar]
  • 9. Dong XQ, Shen Y, Xu LW, Xu CM, Bi W, Wang XM. Contrast-enhanced ultrasound for detection and diagnosis of renal clear cell carcinoma. Chin Med J (Engl). 2009;122(10):1179-83. [PubMed] [Google Scholar]
  • 10. Pan K-H, Jian L, Chen W-J, Nikzad AA, Kong FQ, Bin X, et al. Diagnostic performance of contrast-enhanced ultrasound in renal cancer: a meta-analysis. Front Oncol. 2020;10:586949. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Porter TR, Abdelmoneim S, Belcik JT, McCulloch ML, Mulvagh SL, Olson JJ, et al. Guidelines for the cardiac sonographer in the performance of contrast echocardiography: a focused update from the American Society of Echocardiography. J Am Soc Echocardiogr. 2014;27(8):797-810. [DOI] [PubMed] [Google Scholar]
  • 12. Abramowicz JS. Ultrasound contrast media and their use in obstetrics and gynecology. Ultrasound Med Biol. 1997;23(9):1287-98. [DOI] [PubMed] [Google Scholar]
  • 13. Abramowicz JS. Ultrasonographic contrast media: has the time come in obstetrics and gynecology? J Ultrasound Med. 2005;24(4):517-31. [DOI] [PubMed] [Google Scholar]
  • 14. Pop CM, Mihu D, Badea R. Role of contrast-enhanced ultrasound (CEUS) in the diagnosis of endometrial pathology. Clujul Med. 2015;88(4):433-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Sidhu PS CV, Dietrich CF, Gilja OH, Saftoiu A, Bartels E, Bertolotto M, et al. The ESFUMB guidelines and recommendations for the clinical practice of contrast-enhanced ultraound (CEUS) in non-hepatic applications: update 2017. Ultraschall Med (Stuttgart, Germany: 1980). 2018;39(2):43. [DOI] [PubMed] [Google Scholar]
  • 16. Whiting PF, Rutjes AWS, Westwood ME, Mallett S, Deeks JJ, Reitsma JB, et al. QUADAS-2: a revised tool for the quality assessment of diagnostic accuracy studies. Ann Intern Med. 2011;155(8):529-36. [DOI] [PubMed] [Google Scholar]
  • 17. Liu Y, Tian JW, Xu Y, Cheng W. Role of transvaginal contrast-enhanced ultrasound in the early diagnosis of endometrial carcinoma. Chin Med J (Engl). 2012;125(3):416-21. [PubMed] [Google Scholar]
  • 18. Song Y, Yang J, Liu Z, Shen K. Preoperative evaluation of endometrial carcinoma by contrast-enhanced ultrasonography. BJOG. 2009;116(2):294-8; discussion 8-9. [DOI] [PubMed] [Google Scholar]
  • 19. Lieng M, Qvigstad E, Dahl GF, Istre O. Flow differences between endometrial polyps and cancer: a prospective study using intravenous contrast-enhanced transvaginal color flow Doppler and three-dimensional power Doppler ultrasound. Ultrasound Obstet Gynecol. 2008;32(7):935-40. [DOI] [PubMed] [Google Scholar]
  • 20. Liu ZZ, Jiang YX, Dai Q, Yang M, Zhu QL, Zhao DC, et al. Imaging of endometrial carcinoma using contrast-enhanced sonography. J Ultrasound Med. 2011;30(11):1519-27. [DOI] [PubMed] [Google Scholar]
  • 21. Zhou H-l, Xiang H, Duan L, Shahai G, Liu H, Li X-h, et al. Application of combined two-dimensional and three-dimensional transvaginal contrast enhanced ultrasound in the diagnosis of endometrial carcinoma. BioMed Res Int. 2015;2015:292743. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Liu Y, Xu Y, Cheng W, Liu X. Quantitative contrast-enhanced ultrasonography for the differential diagnosis of endometrial hyperplasia and endometrial neoplasms. Oncol Lett. 2016;12(5):3763-70. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23. Su Q, Sun Z, Lv G. Contrast enhanced ultrasound in diagnosis of endometrial carcinoma and endometrial hyperplasia. Cell Mol Biol (Noisy-le-grand). 2018;64(11):88-91. [PubMed] [Google Scholar]
  • 24. Zhang M, Qiu Y, Zhao L, Zhang X, Wang J, Zhang C, et al. Prognostic value of quantitative perfusion parameters by enhanced ultrasound in endometrial cancer. Med Sci Monit. 2019;25:298-304. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Green RW, Epstein E. Dynamic contrast-enhanced ultrasound improves diagnostic performance in endometrial cancer staging. Ultrasound Obstet Gynecol. 2020;56(1):96-105. [DOI] [PubMed] [Google Scholar]
  • 26. Li Z, Zhang P, Shen H, Ding B, Wang H, Li J, et al. Clinical value of contrast-enhanced ultrasound for the differential diagnosis of specific subtypes of uterine leiomyomas. J Obstet Gynaecol Res. 2021;47(1):311-9. [DOI] [PubMed] [Google Scholar]
  • 27. Dorenberg EJ, Jakobsen JA, Brabrand K, Hafsahl G, Smith HJ. The feasibility of contrast-enhanced ultrasound during uterine artery embolization: a pilot study. Cardiovasc Intervent Radiol. 2007;30(5):882-7. [DOI] [PubMed] [Google Scholar]
  • 28. Zhou XD, Ren XL, Zhang J, He GB, Zheng MJ, Tian X, et al. Therapeutic response assessment of high intensity focused ultrasound therapy for uterine fibroid: utility of contrast-enhanced ultrasonography. Eur J Radiol. 2007;62(2):289-94. [DOI] [PubMed] [Google Scholar]
  • 29. Sconfienza LM, Lacelli F, Gandolfo N, Gazzo P, Perrone N, Serafini G. Contrast-enhanced ultrasound (CEUS) assessment of superselective uterine fibroid embolization (SUFE): Preliminary experience. J Ultrasound. 2008;11(4):158-61. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Wang W, Wang Y, Tang J. Safety and efficacy of high intensity focused ultrasound ablation therapy for adenomyosis. Acad Radiol. 2009;16(11):1416-23. [DOI] [PubMed] [Google Scholar]
  • 31. Wang F, Zhang J, Han ZY, Cheng ZG, Zhou HY, Feng L, et al. Imaging manifestation of conventional and contrast-enhanced ultrasonography in percutaneous microwave ablation for the treatment of uterine fibroids. Eur J Radiol. 2012;81(11):2947-52. [DOI] [PubMed] [Google Scholar]
  • 32. Wang W, Wang Y, Wang T, Wang J, Wang L, Tang J. Safety and efficacy of US-guided high-intensity focused ultrasound for treatment of submucosal fibroids. Eur Radiol. 2012;22(11):2553-8. [DOI] [PubMed] [Google Scholar]
  • 33. Lei F, Jing Z, Bo W, Dongmei H, Zhencai L, Xue J, et al. Uterine myomas treated with microwave ablation: the agreement between ablation volumes obtained from contrast-enhanced sonography and enhanced MRI. Int J Hyperthermia. 2014;30(1):11-8. [DOI] [PubMed] [Google Scholar]
  • 34. Henri M, Florence E, Aurore B, Denis H, Frederic P, Francois T, et al. Contribution of contrast-enhanced ultrasound with Sonovue to describe the microvascularization of uterine fibroid tumors before and after uterine artery embolization. Eur J Obstet Gynecol Reprod Biol. 2014;181:104-10. [DOI] [PubMed] [Google Scholar]
  • 35. Wang Y, Wang W, Ye H. Contrast-enhanced ultrasonography assessment of therapeutic efficacy for ultrasound-guided high-intensity focused ultrasound ablation of uterine fibroids: comparison with contrast-enhanced magnetic resonance. J Med Ultrasound. 2014;22(1):22-8. [Google Scholar]
  • 36. Xia M, Jing Z, Zhi-yu H, Yu Y, Yan-li H, Chang-tao X, et al. Research of dose-effect relationship parameters of percutaneous microwave ablation for uterine leiomyomas - a quantitative study. Sci Rep. 2014;4:6469. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. Yu Y, Jing Z, Zhi-yu H, Xia M, Yan-li H, Chang-tao X, et al. Ultrasound-guided percutaneous microwave ablation for adenomyosis: efficacy of treatment and effect on ovarian function. Sci Rep. 2015;5:10034. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38. Zhang Y, Zhang M, Fan X, Mao D. Contrast-enhanced ultrasound is better than magnetic resonance imaging in evaluating the short-term results of microwave ablation treatment of uterine fibroids. Exp Ther Med. 2017;14(5):5103-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39. Wang Y-J, Zhang P-H, Zhang R, An P-L. Predictive value of quantitative uterine fibroid perfusion parameters from contrast-enhanced ultrasound for the therapeutic effect of high-intensity focused ultrasound ablation. J Ultrasound Med. 2018;38(6):1511-7. [DOI] [PubMed] [Google Scholar]
  • 40. Xu C, Tang Y, Zhao Y, Li Y, Feng Q. Use of contrast-enhanced ultrasound in evaluating the efficacy and application value of microwave ablation for adenomyosis. J Cancer Res Ther. 2020;16(2):365-71. [DOI] [PubMed] [Google Scholar]
  • 41. Peng S, Xiong Y, Li K, He M, Deng Y, Chen L, et al. Clinical utility of a microbubble-enhancing contrast (“SonoVue”) in treatment of uterine fibroids with high intensity focused ultrasound: a retrospective study. Eur J Radiol. 2012;81(12):3832-8. [DOI] [PubMed] [Google Scholar]
  • 42. Dorenberg EJ, Hol PK, Jakobsen JA, Ring E. Improved infarction rates in fibroids after the introduction of contrast-enhanced ultrasound during uterine artery embolization. Acta Radiol. 2012;53(1):34-8. [DOI] [PubMed] [Google Scholar]
  • 43. Cheng C-Q, Zhang R-T, Xiong Y, Chen L, Wang J, Huang G-H, et al. Contrast-enhanced ultrasound for evaluation of high-intensity focused ultrasound treatment of benign uterine diseases: retrospective analysis of contrast safety. Medicine. 2015;94(16):e729. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44. Isern J, Pessarrodona A, Rodriguez J, Vallejo E, Gimenez N, Cassado J, et al. Using microbubble sonographic contrast agent to enhance the effect of high intensity focused ultrasound for the treatment of uterine fibroids. Ultrason Sonochem. 2015;27:688-93. [DOI] [PubMed] [Google Scholar]
  • 45. Jiang N, Xie B, Zhang X, He M, Li K, Bai J, et al. Enhancing ablation effects of a microbubble-enhancing contrast agent (“SonoVue”) in the treatment of uterine fibroids with high-intensity focused ultrasound: a randomized controlled trial. Cardiovasc Intervent Radiol. 2014;37(5):1321-8. [DOI] [PubMed] [Google Scholar]
  • 46. Orsi F, Monfardini L, Bonomo G, Krokidis M, Della Vigna P, Disalvatore D. Ultrasound guided high intensity focused ultrasound (USgHIFU) ablation for uterine fibroids: do we need the microbubbles? Int J Hyperthermia. 2015;31(3):233-9. [DOI] [PubMed] [Google Scholar]
  • 47. Peng S, Hu L, Chen W, Chen J, Yang C, Wang X, et al. Intraprocedure contrast enhanced ultrasound: the value in assessing the effect of ultrasound-guided high intensity focused ultrasound ablation for uterine fibroids. Ultrasonics. 2015;58:123-8. [DOI] [PubMed] [Google Scholar]
  • 48. Jingqi W, Lu Z, Jun Z, Yuhong M, Wei Y, Lifeng R, et al. Clinical usefulness of the microbubble contrast agent SonoVue in enhancing the effects of high-intensity focused ultrasound for the treatment of adenomyosis. J Ultrasound Med. 2018;37(12):2811-19. [DOI] [PubMed] [Google Scholar]
  • 49. Stoelinga B, Dooper AMC, Juffermans LJM, Postema AW, Wijkstra H, Brölmann HAM, et al. Use of contrast-enhanced ultrasound in the assessment of uterine fibroids: a feasibility study. Ultrasound Med Biol. 2018;44(8):1901-9. [DOI] [PubMed] [Google Scholar]
  • 50. Brölmann H, Sizzie O, Hehenkamp WJ, Rossetti A. Laparoscopic power morcellation of presumed fibroids. Minerva Ginecol. 2016;68(3):11. [PubMed] [Google Scholar]
  • 51. Administration FaD. Laparoscopic uterine power morcellation in hysterectomy and myoectomy: FDA Safety Communication. 2014. [Google Scholar]
  • 52. Dueholm M. Uterine adenomyosis and infertility, review of reproductive outcome after in vitro fertilization and surgery. Acta Obstet Gynecol Scand. 2017;96(6):715-26. [DOI] [PubMed] [Google Scholar]
  • 53. van den Bosch T, de Bruijn AM, de Leeuw RA, Dueholm M, Exacoustos C, Valentin L, et al. A sonographic classification and reporting system for diagnosing adenomyosis. Ultrasound Obstet Gynecol. 2018;53(5):576-82. [DOI] [PubMed] [Google Scholar]
  • 54. Harmsen MJ, Wong FC, Mijatovic V, Griffioen AW, Groenman F, Hehenkamp WJK, et al. Role of angiogenesis in adenomyosis associated abnormal uterine bleeding and subfertility: a systematic review. Hum Reprod Update. 2019;25:647-71. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55. Chen Y, Jiang J, Zeng Y, Tian X, Zhang M, Wu H, et al. Effects of a microbubble ultrasound contrast agent on high-intensity focused ultrasound for uterine fibroids: a randomised controlled trial. Int J Hyperther. 2018;34(8):4. [DOI] [PubMed] [Google Scholar]
  • 56. Schneider M. Characteristics of SonoVue trademark. Echocardiography. 1999;16(7):4. [DOI] [PubMed] [Google Scholar]
  • 57. Brace CL. Radiofrequency and microwave ablation of the liver, lung, kidney and bone: what are the differences: “Organ-specific thermal ablation”. Curr Probl Diagn Radiol. 2009;38(3):135-43. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58. Piscaglia F, Nolsoe C, Dietrich CF, Cosgrove DO, Gilja OH, Bachmann Nielsen M, et al. The EFSUMB guidelines and recommendations on the clinical practice of contrast enhanced ultrasound (CEUS): update 2011 on non-hepatic applications. Ultraschall Med (Stuttgart, Germany: 1980). 2012;33(1):33-59. [DOI] [PubMed] [Google Scholar]
  • 59. Torkzaban M, Machado P, Gupta I, Hai Y, Forsberg F. Contrast-enhanced ultrasound for monitoring non-surgical treatments of uterine fibroids: a systematic review. Ultrasound Med Biol. 2021;47(1):3-18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60. Dietrich CF, Kratzer W, Strobe D, Danse E, Fessl R, Bunk A, et al. Assessment of metastatic liver disease in patients with primary extrahepatic tumors by contrast-enhanced sonography versus CT and MRI. World J Gastroenterol. 2006;12(11):1699-705. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61. Trillaud H, Bruel JM, Valette PJ, Vilgrain V, Schmutz G, Oyen R, et al. Characterization of focal liver lesions with SonoVue-enhanced sonography: international multicenter-study in comparison to CT and MRI. World J Gastroenterol. 2009;15(30):3748-56. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62. Romanini L, Passamonti M, Aiani L, Cabassa P, Raieli G, Montermini I, et al. Economic assessment of contrast-enhanced ultrasonography for evaluation of focal liver lesions: a multicentre Italian experience. Eur Radiol. 2007;17(Suppl 6):7. [DOI] [PubMed] [Google Scholar]

Articles from Ultrasonic Imaging are provided here courtesy of SAGE Publications

RESOURCES