Background This study aimed to describe the contrast-enhanced ultrasound (CEUS) features of canine hepatocellular carcinoma (HCC) in relation to cellular differentiation and lesion size.
Methods Sixty dogs with a cytological diagnosis of HCC and that underwent a CEUS examination were retrospectively selected. The wash-in and wash-out patterns of contrast enhancement, along with the time to wash-in and the time to wash-out, of each lesion were recorded. A dimensional cut-off value of 3 cm was adopted for classification.
Results Cellular differentiation had a significant influence on both wash-in (chi-squared=16.99; P<0.001) and wash-out (chi-squared=10.9; P=0.004) patterns of contrast enhancement. Lesion size had a lower, but still significant, influence on both wash-in (chi-squared=12.7; P=0.005) and wash-out (chi-squared=7.42; P=0.024) patterns. A homogeneous hyperenhancement in the arterial phase followed by homogeneous wash-out were suggestive of a well-differentiated HCC. The cellular differentiation of lesions with inhomogeneous hyperenhancement or hypoenhancement/no enhancement as well as an inhomogeneous wash-out or no wash-out could not be inferred.
Conclusions No significant difference in the time to wash-in and the time to wash-out in relation to cellular differentiation or lesion size was evident. CEUS has the potential to improve efficiency in the diagnosis of HCCs in dogs.
- hepatocellular carcinoma
- contrast-enhanced ultrasound
This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, an indication of whether changes were made, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
Statistics from Altmetric.com
Contrast-enhanced ultrasound (CEUS) is a specialised application of B-mode ultrasonography using an intravascular contrast agent to increase the backscattering of blood, thus allowing a real-time evaluation of the vascularisation of different organs or lesions.1 In human medicine, detailed guidelines on the use of CEUS both for hepatic2 and extrahepatic3 diseases have been proposed and are constantly updated following new advances in the literature.4 CEUS is reported to have a high sensitivity and specificity in the distinction between benign and malignant liver masses.5–8 Moreover, CEUS showed promise in the distinction between inflammatory and non-inflammatory liver disease,9 and in the diagnosis of gall bladder disease.10 The possible applications of CEUS in the diagnosis of extrahepatic11–13 pathologies have also been studied in veterinary clinical settings. However, to date, no detailed guidelines on the use of this diagnostic tool in dogs have become available.
Primary hepatic neoplasia is uncommon in dogs and accounts for 1.5 per cent of all the neoplasms in the canine species14 and hepatocellular carcinoma (HCC) is the most common form of liver neoplasia in dogs.15 HCCs are classified on the basis of their gross morphology as massive, nodular and diffused,15 as well as on the basis of cellular differentiation as: poorly, moderately or well differentiated. The prognosis and treatment options for HCC are related to morphology and histology.14 Furthermore, poorly differentiated HCCs are reported to have a higher metastatic rate compared with more differentiated HCCs.16
In human medicine, the use of CEUS in the diagnostic workflow of HCCs is still debated, mostly due to factors such as lesion size and cellular differentiation, which are reported to influence the patterns of contrast medium distribution within the lesion.17–19 To the best of the authors’ knowledge, the effects of lesion size and cellular differentiation on the HCC patterns of contrast enhancement have not yet been elucidated in dogs. The possibility to accurately predict the cellular differentiation of HCCs in dogs could help the clinician in the choice of the optimal treatment for each patient. In particular, radiofrequency or thermal ablation20–22 alone, or in combination with surgical resection, could be used for the treatment of less aggressive forms of HCC. The treatment options for HCC in human beings depend on the size, the number of tumours, the stage and the cause of cirrhosis.23
The aims of the present study were therefore:
To describe the influence of cellular differentiation, as evaluated by cytology, on the perfusion characteristics of HCCs.
To evaluate the effect of lesion size, regardless of cellular differentiation, on the patterns of HCC contrast medium distribution.
Dogs referred for specialty CEUS examination, between January 2010 and June 2018, with a cytological diagnosis of HCC were retrospectively included in the study. Complete signalment was recorded for each patient.
The inclusion criteria were:
Cytological diagnosis of HCC and cellular differentiation of the lesion reported clearly by the pathologist.
Cytological diagnosis performed within one month of the CEUS examination.
The exclusion criteria were:
Multiple lesions in the liver evident in B-mode ultrasound.
Cytological diagnosis other than HCC.
HCC included only within differential diagnoses without any evidence of cellular differentiation.
Patients receiving chemotherapy for HCC or other malignancies.
Thrombosis of the hepatic vein, congenital or acquired vascular abnormalities, due to possible haemodynamic interference.
CEUS image acquisition
All patients were fasted for at least eight hours before the CEUS examination. All the examinations were performed by two veterinarians (GR and PB) each with more than 20 years’ experience in veterinary ultrasonography. Ultrasonographic examinations were performed using a GE Logiq E9 (GE Medical Systems, Milwaukee, Wisconsin, USA), an Esaote MyLab70 Gold (Esaote Italia, Milan, Italy) or an Esaote Twice (Esaote Italia, Milan, Italy) ultrasound machine on unsedated dogs positioned in dorsal recumbency. The mechanical index was set to a very low value (0.2) to prevent bubble disruption. The contrast medium (Sonovue, Bracco Imaging BV, Geneva, Switzerland) was manually administered intravenously through an 18/20G catheter inserted in the cephalic vein at the dose of 0.05 ml/kg and all the examinations were stored digitally. Each patient was scanned continuously for at least two minutes.
Ultrasound-guided fine needle aspiration using a 21 g needle attached to a 2.5 g syringe for cytology was performed in all cases after the completion of the CEUS to avoid bleeding artefacts. Cytology was always performed, using a fine needle aspiration technique, after the CEUS examination to avoid artefacts caused by bleeding. The cellular differentiation of HCC was determined according to the available literature.24 25 Lesions were classified as poorly or moderately differentiated based on the presence of marked or moderate malignancy features in the hepatocytes, such as: anisokaryosis, anisocytosis, anisonucleoliosis, macrokaryosis, macronucleoliosis.25 HCCs were classified as being well differentiated if the following cytological features were present: dissociation of hepatocytes, acinar of palisading cytoarchitectures of the neoplastic hepatocytes, presence of naked nuclei and capillaries, mild anisokaryosis and anisocytosis, multinucleated cells, and increased nucleus to cytoplasm ratio.24
B-mode ultrasound and contrast-enhanced image analysis
All the ultrasonographic examinations were reviewed separately by the same two operators (TB and GR); the final features were determined after a consensus discussion. The lesions were classified as: hypoechoic, isoechoic, hyperechoic or as having mixed echogenicity, according to their echogenicity in comparison to the surrounding liver parenchyma.
The CEUS examinations were reviewed separately the two operators. Final features were determined after a consensus discussion. The entire procedure was divided into: (1) an arterial phase (0–15 seconds from contrast medium injection), (2) a portal phase (15–60 seconds from contrast medium injection) and (3) a late phase (60–120 seconds from contrast medium injection), in accordance with the available literature.5
The time to wash-in and the time to wash-out were calculated using purpose-developed MATLAB script generating time-intensity curves from the .avi examination files.
Using purpose-developed MATLAB script generating time-intensity curves from the .avi examination files the time-intensity curves of two regions of interest (ROI) were calculated. One ROI was placed on the lesion and the other one was placed on an ultrasonographically normal portion of the liver parenchyma.
The wash-in was considered as the enhancement pattern of each lesion immediately after contrast medium injection. The echogenicity of the lesion during the wash-in was compared with that of the surrounding liver tissue. The wash-in enhancement patterns were defined as follows: (1) hyperenhancement if the lesion was more enhancing than the remainder of the liver parenchyma; (2) hypoenhancement if the lesion was less enhancing than the remainder of the liver parenchyma; (3) isoenhancement, if the lesion was as enhancing as the remainder of the liver parenchyma. Hyperenhancing wash-in was further classified as: (a) homogeneous, (b) inhomogeneous or (c) peripheral, depending on the intralesional distribution of contrast medium. In hyperenhancing/isoenhancing lesions, the time to wash-in, defined as the first time contrast became visible within the lesion after injection, was recorded.
Only lesions with a hyperenhancing wash-in were considered as having a wash-out. Wash-out was defined as the lesion becoming less enhancing than the remainder liver parenchyma during the examination. If the lesion was still isoenhancing to the liver parenchyma at the end of the examination (two minutes), it was classified as having no wash-out. In inhomogeneous hyperenhancing lesions, observation of the wash-out was focused on the area showing hyperenhancement. A progressive and synchronous wash-out in the entire lesion was defined as homogeneous and anything other than this was defined as heterogeneous. The time to wash-out, considered as the time for the lesion to become less enhancing than the surrounding liver parenchyma, was also recorded.
Statistics and data analysis
The lesions were divided into two groups, based on their maximum diameter, using a cut-off value of 3 cm to evaluate the effect of the tumour size on the CEUS features of HCC. This procedure was adapted from similar publications evaluating HCC contrast-enhancement patterns in human patients.18 The effects of cellular differentiation and tumour size both on the echogenicity of the B-mode, along with the wash-in (homogeneous hyperenhancement, inhomogeneous hyperenhancement, peripheral hyperenhancement and hypoenhancement) and wash-out (homogeneous wash-out, inhomogeneous wash-out and no wash-out) patterns were tested with the chi-squared test or Fisher’s exact method.26 The effect of cellular differentiation and tumour size on the time to wash-in and time to wash-out were analysed using the Kruskal-Wallis test for non-normally distributed data or one-way analysis of variance for normally distributed data. The statistical evaluation was performed using the MedCalc software package (SPSS, Chicago, USA). A P value less than 0.05 was considered statistically significant for each test.
Sixty dogs of varying breeds including: 32 mixed breed, 5 golden retriever, 4 boxer, 4 labrador retriever, 3 beagle, 12 other breeds; 9 entire females (15 per cent), 20 neutered females (33.3 per cent), 23 entire males (38.3 per cent), 8 neutered males (13.3 per cent); median age was 13 years, range 7–16, matched the inclusion criteria. Most of the dogs included in this study were referred for specialty CEUS characterisation of previously ultrasonographically identified liver masses and, therefore, complete clinical records for most of the patients were not available.
Sixteen dogs were diagnosed with poorly differentiated HCC (9 males – median age 14 years, range 12–16; 7 female – median age 14 years, range 13–16), 6 with moderately differentiated HCC (1 male – age 13 years; 5 females – median age 11 years, range 11–13) and 38 with well-differentiated HCC (20 males – median age 12 years, range 7–16; 18 females – median age 14 years, range 13–16). Due to the relatively low number of moderately differentiated HCCs in the database, poorly differentiated HCCs and moderately differentiated HCCs were considered as a single category, subsequently named as ‘moderately/poorly differentiated’, in the analysis. All data (lesion size, time to wash-in and time to wash-out) were non-normally distributed and therefore differences between groups were always tested with the Kruskal-Wallis test. Mean±SD lesion size was 6.7±3.7 cm (range 0.6–20 cm) and no statistically significant differences in the dimensions of moderately/poorly differentiated and well-differentiated HCCs were evident (chi-squared=3.38, P=0.063). A multiple comparison graph with the dimensions of well-differentiated and moderately/poorly differentiated lesions is shown in figure 1.
B-mode ultrasonographic image analysis
There were no clear differences in the B-mode features either in relation to cellular differentiation or lesion size. The results of the chi-squared test showed distribution of the B-mode features as not significantly different (chi-squared=3.360; P=0.339) between well-differentiated and moderately/poorly differentiated HCCs. There was also no significantly different distribution of the B-mode features in relation to lesion size (chi-squared=3.904; P=0.272). Differences in the proportion of cases showing individual B-mode features based on lesion size and cellular differentiation have also been calculated and are reported in table 1.
Wash-in enhancement patterns and time to wash-in
Hyperenhancement in the arterial phase was the most common feature of HCC (regardless of cellular differentiation and lesion size) and was evident in 86.6 per cent (52/60) of the cases included in this study. Nonetheless, four well-differentiated and four moderately/poorly differentiated HCC cases (13.4 per cent of the total) were hypoenhancing with no significant differences in relation to cellular differentiation or lesion size. Interestingly, none of the lesions was isoenhancing to the liver parenchyma during wash-in. The number of HCC cases showing each wash-in enhancement pattern as classified by cellular differentiation and lesion size is reported in table 2. Multiple comparison graphs with the time to wash-in in relation to cellular differentiation and lesion size are reported in figures 2 and 3, respectively. The results of the chi-squared test showed distribution of the contrast enhancement patterns as significantly different (chi-squared=16.99; P<0.001) between well-differentiated and moderately/poorly differentiated HCCs. There was also a significantly different distribution of the contrast enhancement patterns in relation to lesion size (chi-squared=12.7; P=0.005). No significant differences in the time to wash-in in relation to cellular differentiation (chi-squared=0.02; P=0.865) or lesion size (chi-squared=0.08; P=0.933) were evident.
Wash-out patterns and time to wash-out
The number of HCC cases showing wash-out in the arterial, portal or late phase, or without wash-out, classified by cellular differentiation and lesion size, is reported in table 3. The results of the chi-squared test showed no differences in the phase in which wash-out started based on cellular differentiation (chi-squared=0.251; P=0.882) or lesion size (chi-squared=0.170; P=0.917). There were no statistically significant differences between well-differentiated and moderately/poorly differentiated HCCs neither in the individual contrast phase in which wash-out was evident (arterial, portal or late phase, or no wash-out) (table 3), nor in the time to wash-out (chi-squared=1.778; P=0.181). The lesion size resulted as influential (chi-squared=1.29; P=0.255). Multiple comparison graphs with the time to wash-out in relation to cellular differentiation and lesion size, respectively, are depicted in figures 4 and 5.
There was a statistically significant difference in the number of HCC cases showing different wash-out enhancement patterns (homogeneous, inhomogeneous, no wash-out) both based on cellular differentiation (chi-squared=10.9; P=0.004) and lesion size (chi-squared=7.42; P=0.024); indeed, homogeneous hyperenhancement was more frequently associated with well-differentiated HCCs while inhomogeneous hyperenhancement was more frequently associated with moderately/poorly differentiated HCCs. No differences were evident for lesions showing peripheral enhancement and hypoenhancement. Moreover, smaller lesions showed more frequently homogeneous hyperenhancement while larger lesions showed more frequently inhomogeneous hyperenhancement. Differences in the proportion of cases showing individual wash-out patterns (homogeneous, inhomogeneous and no wash-out) based on lesion size and cellular differentiation have also been calculated and are reported in table 4. Although significant, the influence of lesion size on wash-out pattern was lower than that of cellular differentiation, and only lesions with a homogeneous hyperenhancement showed significant differences related to lesion size. Interestingly, five well-differentiated HCCs with homogeneous wash-in had an inhomogeneous wash-out (n=3) or no-wash-out (n=2).
Examples of the time-intensity curves generated using the MATLAB script in lesions demonstrating different wash-in and wash-out patterns are presented in figures 6–9. The CEUS images of: (1) a lesion showing homogeneous hyperenhancing wash-in and homogeneous hypoenhancing wash-out, (2) a lesion showing inhomogeneous hyperenhancing wash-in and homogeneous isoenhancement in the late phase (no -wash-out) and (3) a lesion showing hypernhancement during wash-in and isoenhancement during wash-out (no wash-out) are reported in figures 10–12, respectively.
In human patients hyperenhancement in the arterial phase is recorded in 97 per cent of HCCs regardless of cellular differentiation or lesion size.18 The authors believe that the relatively higher proportion of hypoenhancing lesions (13.4 per cent) evaluated in this study might be due both to the higher dimensional variability of the collected lesions (larger lesions more likely have necrotic areas) that induce an unpredictable influence on the patterns of contrast enhancement18 or, possibly, to an inherent higher proportion of hypovascular HCCs in the canine species. In human medicine, CEUS is often performed as part of the diagnostic process for patients undergoing liver transplantation but, following the Milan criteria, patients with lesions larger than 5 cm are usually excluded from the above surgical procedure.27
As a result of the statistical analyses, homogeneous hyperenhancement is suggestive of a well-differentiated HCC (table 1) (odds ratio (OR) 31.16 per cent, 95 per cent CI 3.68 per cent to 263.83 per cent). The significantly higher prevalence of inhomogeneous enhancement in moderately/poorly differentiated HCCs (50.5 per cent; 11/18) than in well-differentiated ones (18.4 per cent; 7/38) suggests that such a feature is more frequently associated with aggressive lesions (OR: 6.06 per cent, 95 per cent CI 1.17 per cent to 21.38 per cent). The number of well-differentiated and moderately/poorly differentiated lesions having peripheral enhancement was not significantly different, indicating central necrosis as not clearly associated with lesion aggressiveness. It is the authors’ belief that, in such cases, the use of CEUS can still provide valuable information regarding lesion morphology and might help the ultrasonographer in selecting the most appropriate regions to be sampled. Interestingly similar patterns of contrast enhancement in relation to cellular differentiation and lesion type are reported in human patients18 in which identification of cellular differentiation of HCCs is important for the choice of the best treatment option.28
Moderately/poorly differentiated HCCs only had inhomogeneous wash-out or no wash-out whereas well-differentiated HCCs displayed all the possible wash-out patterns. Prospectively lesions displaying homogeneous wash-out are very likely to be well-differentiated HCCs while the cellular differentiation of HCCs displaying inhomogeneous or no wash-out cannot be predicted through CEUS alone.
The proportion of lesions showing inhomogeneous wash-out or no wash-out displayed no differences based on lesion size. In human patients, the time to wash-out is reported to be significantly influenced both by cellular differentiation and lesion size,18 with moderately/poorly differentiated and larger HCCs having the shortest time to wash-out. Interestingly, no differences in time to wash-out in relation to cellular differentiation or lesion size were evident in the present study (figure 5). It is the authors’ opinion that such a difference could be inherent to the study populations considered in the two studies (60 v 276 patients). The inclusion of a larger and more homogeneous caseload could provide more detailed information regarding the HCC wash-out time in dogs.
As a result of the present study most of the well-differentiated HCCs showed a homogeneous hyperenhancement in the arterial phase followed by homogeneous wash-out. Indeed, only one moderately/poorly differentiated HCC showed homogeneous hyperenhancement and no moderately/poorly differentiated HCCs showed homogeneous wash-out. On the other hand, the cellular differentiation of lesions with inhomogeneous hyperenhancement or hypoenhancement/no enhancement as well as an inhomogeneous wash-out could not be inferred. These results are only partially in agreement with previous reports5 that describe hypoenhancement in the portal or the late phase as a distinctive characteristic of malignant nodules. A straightforward comparison of the results of the present study with the reported CEUS features of liver nodules in dogs5 7 is, at this moment in time, very difficult. Indeed, in the study by O’Brien et al,5 the number of HCCs included (n=1) is insufficient for making a reliable comparison, while in the study by Nakamura et al,7 a contrast medium called Sonazoid was used. This is taken up by macrophages and Kupffer cells and therefore has a very different diffusion kinetic from Sonovue, which is purely intravascular. Kutara et al,29 described the perfusion characteristics, using a contrast agent called Leviovist (that has a diffusion kinetic similar to Sonazoid), in eight canine HCCs. In that study all the HCCs displayed hyperenhacement in the arterial phase. On the other hand, in the portal phase, four HCCs displayed hypoenhancement, and four displayed hyperenhancement to the liver parenchyma, thus, at least partially, highlighting the variable CEUS features of HCCs, also in the dog described in the this study.
There is a remarkable overlapping of the CEUS features of HCCs described in the present study with the CEUS features of other neoplasms described in other papers.5–8 For example, Ivancic et al8, described that most of the haemangiosarcomas reported in their study were hypoenhancing in all the phases, a feature that was also found in eight HCCs of the present study cases. Further studies, possibly including a large number of cases, are required to determine the characteristic CEUS features of each tumour type.
One of the main limitations of this work is that most of the lesions were diagnosed only through cytology, which is reported to have a lower accuracy than histopathology in the evaluation of liver masses.30 Cytology is reported to have a low sensitivity (34.8 per cent) but an extremely high positive predictive value (100 per cent) for HCC.30 It should be stressed that all the cases in which cytopathological results were not unequivocal (ie, when HCC was included only within differential diagnoses) were excluded from the present study. Nevertheless, hyperplastic nodules or adenomas cannot be completely ruled out if the lesion has the cytological characteristics of a well-differentiated HCC.24 Benign liver nodules5 (such as adenomas or hyperplastic nodules) are reported to be mostly isoechoic to the liver parenchyma in all phases (15/16 cases included in the study by O’Brien et al and 5/6 in the study by Nakamura et al). None of the cases included in this study showed such CEUS features. The characteristic CEUS features of the liver are due to the peculiar vascularisation of this organ. Therefore, lesions that retain the normal hepatic vasculature (such as adenomas and hyperplastic nodules) are more likely to show the same CEUS features of the normal liver. On the contrary, more aggressive and disruptive lesions, such as HCCs, are significantly related to different CEUS features.
A possible limitation is that the cytological specimens were evaluated by the different pathologists working in the two institutions included in the study but were not reviewed by a single pathologist for this study. In this way some interobserver variability in the classification of the samples might have occurred.
Another important limitation is that the conditions of the liver parenchyma were not evaluated in any study subject. The World Federation for Ultrasound in Medicine and Biology clinical practice recommendations for the application of CEUS to the diagnosis of liver diseases in human medicine make a clear distinction between the CEUS features of HCCs in the non-cirrhotic and the cirrhotic liver.3 Nevertheless, more recent studies18 19 showed no significant influence of the hepatic background on the CEUS characteristics of HCCs.
The influence of both cellular differentiation and lesion size on the wash-in and the wash-out patterns suggests that other diagnostic tools, such as cytology or histopathology, should be used along with CEUS in the diagnosis or follow-up of HCC. To conclude, CEUS might be useful as an ancillary imaging technique in the diagnosis of liver masses or as an alternative tool when cytology cannot be performed safely (eg, when the lesion is near a main vessel, or when the patient has clotting problems). Another possible application of CEUS is in the non-invasive follow-up of already diagnosed lesions. Indeed, a variation in the CEUS features of an HCC in time, for example changing from homogeneous to inhomogeneous hyperenhancement, might suggest a transition from a well-differentiated to a moderately/poorly differentiated HCC.
Funding The present paper is part of a project funded by a Research Grant from the Department of Animal Medicine, production and Health – MAPS, University of Padua, Italy: SID- Zotti 2018 (€ 32.000; Application of deep-learning algorithms in pet animals diagnostic imaging).
Competing interests None declared.
Patient consent for publication Not required.
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement All data relevant to the study are included in the article.
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.