Abstract
Understanding diseases that affect the male reproductive system of dogs and cats is important for improving their health and quality of life. Imaging techniques, such as ultrasound and X-rays, play a fundamental role in the evaluation of this system. They help veterinarians detect problems in the testicles, prostate, and other reproductive organs of dogs and cats. In recent years, advanced ultrasound methods, such as Doppler, elastography, and contrast-enhanced ultrasound, have become more accessible and allow earlier and more accurate diagnosis. Although definitive diagnosis of neoplastic lesions depends on cytological or histopathological examinations, radiography and advanced ultrasonography contribute significantly to early detection and malignancy characterization. This literature review explores the main imaging techniques used in the investigation of malignant lesions in the male reproductive tract of dogs and cats, namely radiography, B-mode and Doppler ultrasonography, elastography, and contrast-enhanced ultrasonography (CEUS). The goal is to help veterinarians make better decisions and improve care for their patients. The integration of these modalities has become well established in human medicine and shows growing applicability in veterinary practice, allowing for real-time, non-invasive assessment of the testes, prostate, penis, and scrotal structures. The compiled data highlight the potential of combining different imaging modalities to improve diagnostic accuracy and provide clinical and surgical support in the management of malignant lesions affecting the male reproductive tract in dogs and cats.
Keywords: radiography, reproduction, small animals, tumors, ultrasound
Introduction
The male reproductive system of dogs and cats comprises the organs involved in the production, transport, and storage of male gametes (spermatozoa), including the scrotum, testes, epididymides, spermatic cords, penis, urethra, and accessory sex glands (prostate and bulbourethral glands) (Konig and Leibich, 2016).
Lesions of the male reproductive tract are frequently reported in dogs (Foster, 2012). The testis is the second most common site for tumor development in male dogs. In contrast, prostatic tumors are uncommon in this species. Testicular and prostatic tumors are rarely reported in cats (McEntee, 2002). Urethral and penile neoplasms are relatively rare, with transmissible venereal tumors (TVTs) and squamous cell carcinomas being the most common neoplasms in male dogs at these sites (Hall et al., 1976; McEntee, 2002). Imaging findings related to the evaluation of the spermatic cord are scarce in the literature (Mantziaras, 2020).
Diagnostic imaging is recognized as one of the most important tools for assessing the reproductive tract in small animals (Mantziaras, 2020). This review aims to describe the use of radiography and ultrasonography, as well as advanced imaging modalities, as diagnostic tools for detecting malignancy in lesions of the male reproductive system in dogs and cats.
Applicability of radiology
Despite advances in various imaging modalities, radiography remains a widely used technique due to its low cost, rapid execution, and availability in veterinary facilities, in addition to its relatively simpler interpretation, especially when compared to ultrasonography (Meomartino et al., 2021).
Radiography can be used to assess the size, shape, contour, and location of the prostate in dogs (Atalan et al., 1999). In general, the most common radiographic finding associated with prostatic disorders in dogs is organ enlargement (Johnston et al., 1991). However, radiographically visualized lesions are nonspecific, and it is not possible to determine whether the observed changes are due to hyperplasia, infection, or neoplasia (Atalan et al., 1999). Prostatic enlargement may present as either symmetrical or asymmetrical. Inflammatory diseases/prostatitis (Figure 1) and hypertrophy typically result in symmetrical, circumferential enlargement, whereas asymmetrical enlargement is usually associated with cysts, abscesses, or neoplasms (Johnston et al., 1991).
Figure 1. Contrast radiography in lateral (A) and ventrodorsal (B) projections revealing prostatitis and paraprosthetic abscess. The prostate is located intra-abdominally, exhibiting increased dimensions and irregular contour demonstrated by contrast extravasation from the prostatic urethra (arrows). Image kindly provided by Douglas Mattei and Letícia Pina, CEMEV.
In the ventrodorsal projection, the normal prostate should not exceed 50% of the width of the pelvic inlet. In lateral projections, the proportion occupied by the gland should not exceed 70% of the distance between the sacral promontory and the pubic bone. In cases of marked prostatomegaly, occupying more than 90% of the sacropubic distance, neoplasia, abscess, or prostatic cyst should be considered as possible differential diagnoses (Feeney et al., 1987). Radiographic assessment of prostatic length may be as useful as ultrasonographic measurement, as a strong correlation has been observed between the lengths obtained by both methods (Johnston et al., 1991).
The evaluation of prostatic margins can significantly contribute to the differentiation among various conditions. Poorly defined or irregular margins are frequently observed in cases of neoplasia or abscesses, reflecting aggressive and infiltrative processes. In contrast, well defined and smooth margins are common features of benign prostatic hyperplasia (BPH) and other slowly progressing, non-invasive conditions. More aggressive processes, whether neoplastic or infectious, may invade or penetrate the prostatic capsule and trigger an inflammatory response in the adjacent periprostatic tissues (Johnston et al., 1991).
Although radiography is not the most commonly used technique currently for the evaluation of prostatic diseases, it complements the diagnostic investigation regarding the topography, enlargement, or calcification of the prostate, as well as involvement of adjacent bony structures (vertebral bodies), lungs, and regional lymph nodes (iliac) due to metastatic neoplastic processes (Smith, 2008; Lévy et al., 2014) (Figure 2). Variations in the radiographic density of the prostate are uncommon. Punctate mineralizations are associated with benign prostatic concretions, abscesses, or neoplasms. In castrated dogs, prostatic mineralization is highly associated with neoplasia, with a positive predictive value of 100%, negative predictive value of 50%, specificity of 100%, and sensitivity of 84% (Bradbury et al., 2009). In intact animals, prostatic mineralizations may or may not be associated with malignant processes, showing a positive predictive value of 22%, negative predictive value of 96%, sensitivity of 67%, and specificity of 77% (Bradbury et al., 2009).
Figure 2. Prostatic carcinoma in the cat. (A) Radiograph in the lateral view showing the cranial displacement of the urinary bladder possibly associated with a prostatic enlargement (dashed line); (B) Ultrasonography of the enlarged prostate in longitudinal view (calipers).
When radiographic masses are detected in the caudal abdomen, retrograde urethrography and positive contrast cystography can be used to locate the bladder and prostate and to distinguish these organs from others; however, they do not provide specific information regarding the etiology of the diseases. Additionally, contrast radiographs (Figure 1) can be employed to determine whether cystic structures are located within the prostate or in the periprostatic region (Assis et al., 2015).
Contrast medium extravasation into the prostate is nonspecific and may occur under normal conditions. However, in the presence of lesions communicating with the urethra, contrast leakage can appear as large, irregular cavitations of contrast accumulation with either rough or smooth margins, potentially indicating neoplastic processes. The absence of contrast extravasation does not exclude prostatic abnormalities. Contrast filling defects at the proximal end of the urethra may be associated with transitional cell carcinoma (Johnston et al., 1991).
Radiography is seldom used for the evaluation of intrascrotal diseases due to the testes, epididymides, and scrotum having radiographic densities similar to those of the surrounding soft tissues (Johnston et al., 1991). Additionally, scrotal enlargement may be observed; however, it is not possible to distinguish between a testicular mass, intrascrotal fluid, or scrotal thickening (Russo et al., 2021).
The possibility of a neoplastic ectopic testis should be considered when radiographic evaluation reveals abdominal masses in animals with no history of castration and in which testicular absence in the scrotum is confirmed by palpation. For radiographic characterization, the neoplastic abdominal testis must be sufficiently enlarged. When visible radiographically, it is most commonly located between the kidney and the inguinal canal, exhibiting soft tissue opacity. Identification and displacement of organs adjacent to the neoplastic abdominal testis should be assessed using both lateral and ventrodorsal projections in order to exclude other potential anatomical sites of origin. Differentiating a testicular neoplasm from masses originating in other abdominal locations can be challenging on radiographs. In some cases, the neoplastic testis may be visualized in the subcutaneous tissue of the caudoventral inguinal region of the abdomen, typically appearing as a soft tissue opacity mass (Birchard and Nappier, 2008; Assis et al., 2015).
Penile neoplasms are relatively rare in dogs (Hall et al., 1976). For penile evaluation, radiographic findings such as soft tissue swelling and osteolysis of the baculum have been reported (Burchell et al., 2014). However, these findings are not specific to any particular tumor type, thus requiring histopathological analysis to determine the nature of the lesion, as previously described in cases of osteosarcoma (Peppler et al., 2009) and hemangiosarcoma of the baculum (Burchell et al., 2014).
Radiography has also allowed the identification of changes such as urethral obstruction and penile edema secondary to soft tissue enlargement, as described in a case histopathologically confirmed as penile lymphosarcoma (Michels et al., 2001). It is important to highlight that the combination of imaging findings, including ultrasonography, plain radiography, and contrast studies, with histological evaluation is essential for the diagnosis and characterization of penile neoplasms (Figure 3).
Figure 3. Lateral radiographic projection of a dog with neoplasia in the os penis. An irregular, mineral radiopaque enlargement is observed adjacent to the proximal portion of the os penis (arrow). Image kindly provided by Luciana Burguese – PROVET.
Applicability of ultrasonography
Ultrasonography is the imaging modality of choice for evaluating the male reproductive tract in dogs and cats, as it allows for the assessment of organ size and parenchymal structure (Figures 4 and 5), as well as guidance for sample collection procedures such as fine-needle aspiration (FNA) or tissue and lesion biopsy (Mantziaras, 2020; Meomartino et al., 2021). B-mode ultrasonography is an effective tool for detecting morphological alterations; however, it presents limitations in evaluating functional aspects and distinguishing between benign and malignant lesions (Volta et al., 2014). In this context, the use of multiparametric approaches, combining different ultrasonographic techniques, has emerged as a promising strategy to improve diagnostic accuracy in the assessment of reproductive health (Mantziaras and Luvoni, 2020).
Figure 4. Ultrasonographic images of a normal canine testicle in the sagittal plane. (A) B-mode evaluation of the homogeneous parenchyma, well defined margins, regular contours and an echogenic mediastinal line (arrow); (B) Color Doppler evaluation of the testicular vascularization with normal distribution of the intratesticular branches (arrowheads) of the testicular artery.
Figure 5. Ultrasonographic images of a normal canine prostate in transverse (A) and longitudinal (B) sections, showing the measurements taken during its evaluation.
Testicular tumors, illustrated in Figure 6, are common in dogs, particularly in older individuals, with reported prevalence ranging from 2% to 60% (McEntee, 2002; Grieco et al., 2008; Orlandi et al., 2022). Ultrasonography enables the detection of focal lesions suggestive of neoplastic involvement or potential testicular torsion (Yates et al., 2003). Sertoli cell tumors are most frequently associated with retained testes, followed by seminomas (England, 1995; Mostachio et al., 2007; Foster, 2012; Bertoldi et al., 2014; Stokowski et al., 2016). Furthermore, the testis may also serve as a site of metastatic spread from other primary neoplasms (Lucas et al., 2012). Testicular tumors are rare in cats (Figure 7); however, interstitial cell tumors, teratomas, Sertoli cell tumors, and seminomas have been reported in this species (McEntee, 2002; Miller et al., 2007).
Figure 6. Ultrasonographic image of intra-abdominal testicular neoplasm in a dog. Mixed testicular tumor (seminoma and Sertoli cell tumor), characterized by a poorly defined, heterogeneous, cavitary mass occupying nearly the entire testicular parenchyma (dashed line).
Figure 7. B-mode ultrasonography of an inguinal ectopic testicle in the cat, in longitudinal view. Arrowheads point to the hypoplastic or atrophic testicle with a hypoechoic parenchyma and ill-defined mediastinal line. Malignancy is among the differentials for this case.
B-mode ultrasonography is widely used for the detection of testicular tumors and allows for the differentiation between intratesticular and extratesticular conditions that lead to scrotal enlargement, as well as the identification of ectopic testes (Pugh and Konde, 1991; Gradil et al., 2007; Orlandi et al., 2022). The development of neoplasia and/or testicular torsion is also associated with cryptorchidism, as illustrated in Figure 8 (Yates et al., 2003). Testicular lesions are more commonly focal rather than diffuse, occupying only part of the testicular parenchyma, and typically present as hypoechoic areas without specific sonographic features that allow differentiation based on tumor type (Orlandi et al., 2022). Additionally, a heterogeneous echotexture may be observed, with or without loss of definition of the mediastinum testis. Hemorrhage and necrosis may also be present, appearing as disorganized hyperechoic or hypoechoic regions. These tumors can cause generalized testicular enlargement, obliteration of the testicular mediastinum and epididymis, and distortion of the normal organ anatomy (Assis et al., 2015).
Figure 8. Ultrasonographic image of a Sertoli cell tumor in an intra-abdominal ectopic testis causing mechanical compression of the caudal vena cava. A well defined, heterogeneous, solid-appearing mass with interspersed cavitary areas is observed overlapping the caudal vena cava, occluding its lumen (arrow).
Although B-mode ultrasonography allows for detailed visualization of the testicular architecture and parenchyma, it does not permit accurate differentiation among Sertoli cell tumors, seminomas, interstitial cell carcinomas, abscesses, or hematomas (Mantziaras, 2020).
The scrotum is a musculocutaneous pouch that houses the testes, epididymides, and deferent ducts. Any tumor involving the skin may potentially affect the scrotum in both dogs and cats (McEntee, 2002). Neoplastic lesions of the scrotum may account for approximately 0.4% of all cutaneous neoplasms (Trappler et al., 2014).
The prostate is the only accessory sex gland in dogs, completely encircling the proximal urethra at the level of the bladder neck and is bilobed in structure. In cats, the prostate has been described as a “rudimentary” organ, presenting as a compact structure composed of tubular glandular epithelium, symmetrically distributed dorsolaterally to the urethra, extending from its cranial portion caudodorsally to the cranial border of the pelvic symphysis. Bulbourethral glands are present in all domestic mammals, with the exception of dogs (Mattoon and Nyland, 2002; Konig and Leibich, 2016).
Although ultrasonography is the imaging modality of choice for evaluating the canine prostate, sonographic findings of prostatic neoplasms are nonspecific and do not allow for differentiation among tumor types (Mantziaras, 2020). In felines, ultrasonographic assessment of the prostate and bulbourethral glands has been scarcely described in the literature (Dimitrov et al., 2010).
Prostatic neoplasms and BPH may initially present with similar ultrasonographic parenchymal features. In advanced stages of neoplasia, the parenchyma may appear heterogeneous, hyperechoic or mixed, with irregular anechoic regions and areas of calcification (Assis et al., 2015). Ultrasonographic evaluation of the medial iliac lymph node may be useful, as enlargement, hypoechogenicity, and possibly increased vascularity can be observed in cases of suspected prostatic inflammation or neoplasia (Mantziaras, 2020). Similar to radiography, the detection of prostatic mineralization by ultrasonography in neutered dogs has a 100% positive predictive value for malignancy (Bradbury et al., 2009).
Malignant lymphoma of the canine prostate is rare and has been reported primarily as a manifestation of multicentric disease rather than as a primary prostatic lymphoma. This type of neoplasm can exhibit a wide variety of ultrasonographic appearances. However, a predominance of hypoechoic lesions, whether diffuse, focal, or multifocal, is notable. Other common features include rounded or irregular margins, absence of mineralization, and ultrasonographic evidence of involvement of multiple organs, with or without lymphadenomegaly. Prostatomegaly was subjectively recorded in all patients, although it was not quantified through objective measurements (Di Donato et al., 2019).
Doppler
Doppler ultrasonography has emerged as an advanced imaging modality for evaluating the reproductive tract of small animals, serving as a useful tool in the assessment of the prostate and testicles, including its applicability as a marker of semen quality and in the differentiation between benign and malignant lesions (Bigliardi et al., 2019; Mantziaras and Luvoni, 2020). However, the various tumor types are not distinguishable using this technique (Bigliardi et al., 2019). Doppler modalities such as color and pulsed Doppler assess the presence and direction of blood flow, as well as provide information on hemodynamic parameters, respectively (Orlandi et al., 2022).
In the evaluation of testicular tumors in dogs using color Doppler imaging, neoplastic lesions (Figure 9) demonstrate increased internal and peripheral blood flow when compared to inflammatory and degenerative lesions. An increased vascular index has been detected in solid tumors, while no blood flow was observed around cysts (Bigliardi et al., 2019).
Figure 9. Ectopic testicle identified in the subcutaneous abdominal region of a 13-year-old Yorkshire dog with unilateral cryptorchidism. (A) Neoplastic findings, evaluated by B-mode ultrasound in the sagittal plane, showing heterogeneous parenchyma, increased dimensions, and evident abnormal vascular walls; (B) Color Doppler shows evident perilesional vascularization and deficient vascularization in the rest of the parenchyma.
Additionally, subtle variations in the tumor vascularization pattern may aid in their differentiation. Sertoliomas exhibited higher pulsatility and resistance indices in the testicular and pampiniform arteries, whereas Leydig cell tumors showed a predominantly peri- and/or intralesional blood flow pattern (Orlandi et al., 2022).
Although the vascular patterns of testicular blood flow in adult cats have already been established (Brito et al., 2015), the literature remains scarce regarding species-specific abnormalities (Trautwein et al., 2024).
Even though adenocarcinomas cause changes in prostatic shape, increased volume, loss of capsular integrity, and heterogeneous echogenicity, with anechoic, mineralized, and nodular areas, Doppler ultrasonography has limitations in differentiating benign from malignant prostatic diseases (Troisi et al., 2015; Mantziaras, 2020).
Elastography
Elastography is a recent ultrasonographic technique that allows for both qualitative and quantitative assessment of tissue stiffness, based on two main categories: strain elastography (which requires external mechanical compression and assesses tissue elasticity) and shear wave elastography (Zappone et al., 2024). Over the past decade, it has been applied to the evaluation of the male reproductive system in dogs and cats, in association with B-mode ultrasonography (Brito et al., 2015; Feliciano et al., 2015).
While this examination is valuable for assessing tissue health, its application presents certain limitations, as lesions of inflammatory or neoplastic origin may alter histological composition in various ways. Nonetheless, the availability of reference values for evaluating structures of the reproductive tract in small animals can support the rapid and non-invasive differentiation between benign and malignant conditions (Feliciano et al., 2015; Zappone et al., 2024). Furthermore, as an ultrasonographic technique, it is frequently integrated into multiparametric assessments, thereby contributing to a more accurate diagnosis (Mantziaras and Luvoni, 2020; Cantisani et al., 2021).
Elastography enhances the diagnosis of testicular neoplasms due to its ability to distinguish between healthy and diseased testes based on tissue stiffness (Zappone et al., 2024), as demonstrated in Figures 10 and 11. This technique is already applied in human medicine for differentiating neoplastic lesions, as well as characterizing malignancy in testicular lesions (Cantisani et al., 2021), showing 100% sensitivity for the detection of testicular tumors, with observed increases in testicular parenchymal stiffness (Aigner et al., 2012).
Figure 10. Qualitative elastography of a testicular Sertolioma. (A) B-mode image showing a coarse-textured, mildly nodular region with a small, poorly defined hypoechoic structure interspersed within the testicular parenchyma; (B) The color map reveals a central area of the lesion with regions of increased stiffness (blue), intermediate stiffness (green), surrounding testicular parenchyma with predominantly lower stiffness (red), and a capsular region with increased stiffness (blue). The elastogram also provides improved delineation between the nodular region and adjacent tissue. Image kindly provided by Marjury Cristina Maronezi.
Figure 11. Quantitative shear wave elastography of a neoplastic ectopic testicle (sertolioma) from the same dog shown in Figure 9. (A) The green box shows the map with high-quality sample acquisition according to the scale bar on the left side (green, high quality; yellow and orange, low quality); (B) The blue box shows the elastogram (red, stiff; blue, soft) with three circular ROIs (1, 2, and 3) for acquiring stiffness values in m/s.
Increased stiffness associated with ultrasonographic findings such as heterogeneity allows for the identification of abnormalities, although these are insufficient for differentiating the type of testicular lesion in dogs (Feliciano et al., 2016). As described in humans, neoplastic testicular lesions in dogs tend to exhibit greater stiffness than non-neoplastic lesions (Glińska-Suchocka et al., 2014). However, tissue stiffness values do not differ among the various types of testicular neoplasms presented (Zappone et al., 2024).
The literature regarding elastographic parameters of diseased prostatic tissue in dogs remains limited (Cintra et al., 2020; Mantziaras and Luvoni, 2020), and to date, no reference values exist for elastographic parameters in cats. Nevertheless, this ultrasonographic technique has been used as an adjunct tool in the diagnosis of prostatic neoplasms in humans (D’Anastasi et al., 2011); similarly to testicular tissue, increased stiffness is observed when compared to the parenchyma of healthy glands or those with benign lesions (Ophir et al., 2002). Likewise, recent studies in dogs have demonstrated increased stiffness in the parenchyma of diseased prostates (Domosławska et al., 2018; Bucci et al., 2023).
Contrast-enhanced ultrasonography (CEUS)
Contrast-enhanced ultrasonography (CEUS) is a technique based on the administration of a contrast agent composed of gas microbubbles encapsulated by a phospholipid membrane, which amplifies the ultrasound signal and has been used to evaluate the male reproductive tract in small animals (Quaia, 2005; Mantziaras, 2020). This imaging modality enables the study of tissue microvascularization and contributes to better identification and characterization of perfusion in lesions and inflammatory processes affecting reproductive organs such as the testicles and prostate, thereby improving diagnostic accuracy when used in conjunction with conventional ultrasonography (Volta et al., 2014; Orlandi et al., 2022).
In addition to being a real-time ultrasonographic technique that is safe, with minimal contraindications and side effects, the most recent contrast agents used in this method, such as sulfur hexafluoride, offer prolonged stability, do not extravasate into the extracellular space, and allow both qualitative and quantitative assessment of normal and altered organ perfusion (Ohlerth and O’Brien, 2007; Haers and Saunders, 2009; Pettina et al., 2024).
Non-neoplastic lesions exhibited mild to moderate homogeneous enhancement, with well defined margins during the wash-in phase (Figures 12D and 12F), which remained consistent during the wash-out phase (Volta et al., 2014). In contrast, neoplastic and inflammatory testicular lesions demonstrated rapid wash-in, prolonged enhancement duration (Figures 12J and 12L), and delayed wash-out. Perfusion parameters were higher in neoplastic lesions, with hyperenhancement being strongly associated with malignancy, showing a sensitivity of 87% and specificity of 100% (Russo et al., 2021). Lesions with persistent internal vascularization and hypoechoic to isoechoic parenchyma were associated with seminomas. Degenerated and atrophic testes exhibited poor contrast enhancement, lower than that of normal tissue (Volta et al., 2014).
Figure 12. B-mode ultrasound and CEUS images of a 13-year-old Yorkshire dog with unilateral cryptorchidism. (A), (C), and (E): testicle located in the scrotal sac, evaluated by B-mode ultrasound in the sagittal plane, showing hypoechoic parenchyma and reduced dimensions. (B), (D) and (F): the same testicle evaluated by CEUS at different contrast phases: immediately after contrast administration (0s) (B); late wash-in (15s) and the moment of detection of microbubbles (dotted lines) in the hypoplastic testicular parenchyma (D); and late peak enhancement (31s) homogeneous, with poor identification of intratesticular branches of the testicular artery in the dorsal portion of the testicle (dotted lines) (F). (G), (I) and (K): ectopic testicle, identified in the subcutaneous region of the abdomen of the same animal, with neoplastic findings (sertolioma), evaluated by B-mode ultrasound in the sagittal plane, showing heterogeneous parenchyma and increased dimensions. (H), (J) and (L): the same testicle evaluated by CEUS at different contrast phases: immediately after contrast administration (0s) (H); early wash-in (8s) and the moment of microbubble detection (dotted lines) in the neoplastic testicular parenchyma (J); and peak enhancement (16s) with early distribution of contrast throughout the parenchyma, showing a nodular lesion, perilesional vessels (arrowheads) and intralesional vessels (L).
One study reported difficulty in differentiating tumor types in testicular lesions based on enhancement patterns alone; however, CEUS outperformed color Doppler, power Doppler, and B-flow by detecting a tumor lesion that these other modalities, including B-mode, failed to identify (Orlandi et al.,2022). Similarly, another study reported that CEUS can differentiate testicular abnormalities and neoplastic lesions, but cannot characterize tumor types (Sinagra et a., 2023).
To date, CEUS has only been used to assess feline testes for the establishment of normal reference parameters (Brito et al., 2015); however, it holds potential as a diagnostic tool to improve ultrasonographic accuracy in identifying benign and malignant conditions affecting this organ, thus supporting earlier clinical and surgical decision-making.
Canine prostatic neoplasms affect elderly individuals, both neutered and intact (Krook, 1954). In cats, these tumors are extremely rare; however, as in dogs, they are typically diagnosed at an advanced stage of the disease, with a poor prognosis due to their aggressiveness and metastatic potential (Caney et al., 1998; Oliveira et al., 2019; Palmieri et al., 2022).
The main challenge in diagnosing prostatic disorders, particularly neoplasms, lies in the limited ability to detect them early and to differentiate benign from malignant processes, due to the overlapping features observed on imaging studies, especially with conventional ultrasonography (Mantziaras, 2020; Russo et al., 2021; Pettina et al., 2024).
Early-stage prostatic neoplasms can be identified through CEUS due to increased blood flow resulting from tumor-induced neoangiogenesis. This is evidenced by rapid asymmetric inflow, increased focal enhancement, and visualization of tortuous intraprostatic vessels, making CEUS the most effective technique when compared to color and power Doppler (Vignoli et al., 2011; Spada et al., 2025).
Specific perfusion patterns have been identified in canine prostates with and without prostatic disease. Time to peak (TTP; seconds) and mean transit time (MTT; seconds) were shorter in prostates affected by pathology; however, no significant differences were observed among the conditions (BPH, prostatitis, and tumors) due to technique-related variables and the lack of well established protocols for each organ, such as patient preparation and ultrasound setting adjustments. In this study, qualitative assessment of diseased prostates allowed differentiation from healthy prostates by the absence of the characteristic centripetal perfusion pattern and the loss of subcapsular arterioles. Furthermore, it was possible to identify distinct vascular patterns associated with conditions such as BPH, prostatitis, adenocarcinoma, and lymphoma (Troisi et al., 2015).
CEUS stands out for its excellent ability to characterize blood perfusion and to detect prostatic lesions that are often missed by conventional methods. For this reason, it represents an advanced and promising imaging tool for early diagnosis, allowing for differentiation between benign and malignant processes. In addition, CEUS is useful for monitoring the regression of these conditions following treatment, as well as for guiding targeted biopsies and radiofrequency ablation procedures, thereby contributing to enhanced diagnostic and therapeutic accuracy (Liu et al., 2008; Russo et al., 2021; Sinagra et al., 2023).
Multiparametric ultrasound (MPUS)
The combination of different imaging techniques for detecting abnormalities in the reproductive system of small animals is already a reality. Although definitive diagnosis is confirmed by cytology or histopathology, the investigation of neoplasms in the reproductive structures of dogs and cats often integrates information obtained from radiographic and ultrasonographic findings, aiming to achieve a more accurate prognosis regarding lesion involvement, adjacent structures, and potential metastatic sites (Michels et al., 2001; Peppler et al., 2009; Burchell et al., 2014).
Due to recent and promising advances in various ultrasonographic modalities, the term Multiparametric Ultrasound (MPUS) Imaging has emerged as a comprehensive approach that combines multiple ultrasonographic techniques such as B-mode, Doppler, elastography, and CEUS (Sidhu, 2015). This has been made possible by technological advancements in imaging equipment alongside the development of novel advanced ultrasound techniques. These methods were not designed to be used in isolation but rather to enhance the diagnostic sensitivity of conventional B-mode ultrasonography (Mantziaras and Luvoni, 2020).
Currently, multiparametric assessment stands out as the most accurate diagnostic method for ultrasonographic evaluation of reproductive health in both humans and small animals (Mantziaras and Luvoni, 2020). It has proven highly valuable in detecting neoplastic lesions and assessing malignancy. In human medicine, it is already used in the evaluation of prostate (Kaneko et al., 2022) and testicular cancer (Cantisani et al., 2021); and studies are underway to establish veterinary applications, including protocols for evaluating reproductive organs in male dogs and cats (Brito et al., 2015; Mantziaras and Luvoni, 2020; Aires et al., 2025).
Conclusion
Imaging methods such as radiography and ultrasonography stand out for being low-cost, accessible, and safe for the patient. Although they have certain limitations, these modalities are important tools for screening and monitoring disorders of the male reproductive system in dogs and cats. The application of advanced ultrasonographic modalities and the multiparametric approach provide valuable diagnostic support, increasing accuracy in the detection of neoplastic lesions and the identification of malignancy-related features in these animals. However, it is important to note that despite their relevance, these methods do not replace cytological or histological examinations, which remain the gold standard for the confirmation and differentiation of benign and malignant neoplasms in the reproductive system of dogs and cats.
Acknowledgments
The authors were supported in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior – Brasil (CAPES) – Finance Code 001, and Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) (process n. 2024/00982-2, 2024/01809-2, and 2025/02548-0).
Funding Statement
Financial support: The authors were supported in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior – Brasil (CAPES) – Finance Code 001. DRG, ACME, and GCLE received funding for this research from the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) (grant numbers 2025/02548-0, 2024/00982-2, and 2024/01809-2, respectively).
Footnotes
Financial support: The authors were supported in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior – Brasil (CAPES) – Finance Code 001. DRG, ACME, and GCLE received funding for this research from the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) (grant numbers 2025/02548-0, 2024/00982-2, and 2024/01809-2, respectively).
Gomes DR, Ercolin ACM, Evangelista GCL, Barros FFPC, Stanquini CS, Debastiani C, Garcia F, Feliciano MAR. Emerging imaging modalities for the diagnosis of malignant lesions of the male reproductive tract in companion animals. Anim Reprod. 2026;23(2):e20250124. https://doi.org/10.1590/1984-3143-AR2025-0124
Data availability statement
No research data was used.
References
- Aigner F, De Zordo T, Pallwein-Prettner L, Junker D, Schäfer G, Pichler R, Leonhartsberger N, Pinggera G, Dogra VS, Frauscher F. Real-time sonoelastography for the evaluation of testicular lesions. Radiology. 2012;263(2):584–589. doi: 10.1148/radiol.12111732. [DOI] [PubMed] [Google Scholar]
- Aires LPN, Gasser B, Del’Aguila-Silva P, Gonçalves JD, Uscategui RAR, Spada S, De Felice D, Russo M, Lima BB, Gimenes LU, Feliciano MAR. Multiparametric ultrasound (MPUS) evaluation of the testes of normozoospermic dogs: a pilot study. Sci Rep. 2025;15(1):7121. doi: 10.1038/s41598-025-91087-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Assis AR, Garcia DAA, Feliciano MAR. In: Diagnóstico por imagem em cães e gatos. 1. Feliciano MAR, Canola JC, Vicente WRR, editors. São Paulo: MedVet; 2015. Sistema reprodutor masculino. pp. 369–409. [Google Scholar]
- Atalan G, Barr FJ, Holt PE. Comparison of ultrasonographic and radiographic measurements of canine prostate dimensions. Vet Radiol Ultrasound. 1999;40(4):408–412. doi: 10.1111/j.1740-8261.1999.tb02133.x. [DOI] [PubMed] [Google Scholar]
- Bertoldi J, Friolani M, Ferioli R. Sertolioma em cão associado a criptoquidismo bilateral: relato de caso. [cited 2025 May 20];Rev Cient Eletr Med Vet. 2014 22:1–10. serial on the Internet. Available from: https://pesquisa.bvsalud.org/portal/resource/pt/vti-16115 . [Google Scholar]
- Bigliardi E, Denti L, De Cesaris V, Bertocchi M, Di Ianni F, Parmigiani E, Bresciani C, Cantoni AM. Colour Doppler ultrasound imaging of blood flows variations in neoplastic and non‐neoplastic testicular lesions in dogs. Reprod Domest Anim. 2019;54(1):63–71. doi: 10.1111/rda.13310. [DOI] [PubMed] [Google Scholar]
- Birchard SJ, Nappier M. Cryptorchidism. Compend Contin Educ Vet. 2008;30(6):325–336. [PubMed] [Google Scholar]
- Bradbury CA, Westropp JL, Pollard RE. Relationship between prostatomegaly, prostatic mineralization, and cytologic diagnosis. Vet Radiol Ultrasound. 2009;50(2):167–171. doi: 10.1111/j.1740-8261.2009.01510.x. [DOI] [PubMed] [Google Scholar]
- Brito M, Feliciano M, Coutinho L, Uscategui R, Simões A, Maronezi M, et al. Doppler and contrast‐enhanced ultrasonography of testicles in adult domestic felines. Reprod Domest Anim. 2015;50(5):730–734. doi: 10.1111/rda.12557. [DOI] [PubMed] [Google Scholar]
- Bucci R, Del Signore F, Vignoli M, Felici A, Russo M, Maresca C, Carluccio A. Canine prostatic serum esterase and strain and 2D‐shear wave sonoelastography for evaluation of normal prostate in dogs: preliminary results. Reprod Domest Anim. 2023;58(9):1311–1319. doi: 10.1111/rda.14435. [DOI] [PubMed] [Google Scholar]
- Burchell RK, Kirberger RM, Janse van Rensberg DD. Haemangiosarcoma of the os penis in a dog: the most common neoplasm of the canine peniss. J S Afr Vet Assoc. 2014;85(1):e1–4. doi: 10.4102/jsava.v85i1.1092. [DOI] [PubMed] [Google Scholar]
- Caney SMA, Holt PE, Day MJ, Rudorf H, Gruffydd‐Jones TJ. Prostatic carcinoma in two cats. J Small Anim Pract. 1998;39(3):140–143. doi: 10.1111/j.1748-5827.1998.tb03619.x. [DOI] [PubMed] [Google Scholar]
- Cantisani V, Di Leo N, Bertolotto M, Fresilli D, Granata A, Polti G, Polito E, Pacini P, Guiban O, Del Gaudio G, Dolcetti V, DʼAndrea V, Di Pierro GB, Verrengia M, Drudi FM, Catalano C. Role of multiparametric ultrasound in testicular focal lesions and diffuse pathology evaluation, with particular regard to elastography: review of literature. Andrology. 2021;9(5):1356–1368. doi: 10.1111/andr.13067. [DOI] [PubMed] [Google Scholar]
- Cintra CA, Feliciano MAR, Santos VJC, Maronezi MC, Cruz IK, Gasser B, Silva P, Crivellenti LZ, Uscategui RAR. Applicability of ARFI elastography in the evaluation of canine prostatic alterations detected by B-mode and Doppler Ultrasonography. Arq Bras Med Vet Zootec. 2020;72(6):2135–2140. doi: 10.1590/1678-4162-12116. [DOI] [Google Scholar]
- D’Anastasi M, Schneevoigt BS, Trottmann M, Crispin A, Stief C, Reiser MF, Clevert DA. Acoustic radiation force impulse imaging of the testes: a preliminary experience. Clin Hemorheol Microcirc. 2011;49(1-4):105–114. doi: 10.3233/CH-2011-1461. [DOI] [PubMed] [Google Scholar]
- Di Donato P, Zweifel R, Koehler K, Golini L, Ressel L, Kramer M, Kiefer I, Lim CK, Ondreka N. Predominance of hypoechoic tissue changes in nine dogs with malignant prostatic lymphoma. Vet Radiol Ultrasound. 2019;60(1):75–80. doi: 10.1111/vru.12686. [DOI] [PubMed] [Google Scholar]
- Dimitrov R, Yonkova P, Stamatova K. Comparative ultrasonogarphic study on prostate and bulbourethral glands of tomcat. Bulg J Agric Sci. 2010;16:521–525. [Google Scholar]
- Domosławska A, Zduńczyk S, Jurczak A, Janowski T. Elastography as a diagnostic tool in the prostate tumour detection in Labrador retriever. Andrologia. 2018;50(10):e13139. doi: 10.1111/and.13139. [DOI] [PubMed] [Google Scholar]
- England GCW. Ultrasonographic diagnosis of non‐palpable Sertoli cell tumours in infertile dogs. J Small Anim Pract. 1995;36(11):476–480. doi: 10.1111/j.1748-5827.1995.tb02785.x. [DOI] [PubMed] [Google Scholar]
- Feeney DA, Johnston GR, Klausner JS, Perman V, Leininger JR, Tomlinson MJ. Canine prostatic disease—comparison of radiographic appearance with morphologic and microbiologic findings: 30 cases (1981–1985) J Am Vet Med Assoc. 1987;190(8):1018–1026. doi: 10.2460/javma.1987.190.08.1018. [DOI] [PubMed] [Google Scholar]
- Feliciano MAR, Maronezi MC, Simões APR, Uscategui RR, Maciel GS, Carvalho CF, Canola JC, Vicente WR. Acoustic radiation force impulse elastography of prostate and testes of healthy dogs: preliminary results. J Small Anim Pract. 2015;56(5):320–324. doi: 10.1111/jsap.12323. [DOI] [PubMed] [Google Scholar]
- Feliciano MAR, Maronezi MC, Simões APR, Maciel GS, Pavan L, Gasser B, Silva P, Uscategui RR, Carvalho CF, Canola JC, Vicente WRR. Acoustic radiation force impulse (ARFI) elastography of testicular disorders in dogs: preliminary results. Arq Bras Med Vet Zootec. 2016;68(2):283–291. doi: 10.1590/1678-4162-8284. [DOI] [Google Scholar]
- Foster RA. Common lesions in the male reproductive tract of cats and dogs. Vet Clin North Am Small Anim Pract. 2012;42(3):527–45, vii. doi: 10.1016/j.cvsm.2012.01.007. [DOI] [PubMed] [Google Scholar]
- Glińska-Suchocka K, Jankowski M, Kubiak K, Spużak J, Dzimira S. Sonoelastography in differentiation of benign and malignant testicular lesion in dogs. Pol J Vet Sci. 2014;17(3):487–491. doi: 10.2478/pjvs-2014-0070. [DOI] [PubMed] [Google Scholar]
- Gradil CM, Yeager A, Concannon PW. In: Recent advances in small animal reproduction. Concannon PW, England G, Verstegen J, editors. Ithaca: IVIS; 2007. Evaluación de los problemas reproductivos del macho canino. [Google Scholar]
- Grieco V, Riccardi E, Greppi GF, Teruzzi F, Iermanò V, Finazzi M. Canine testicular tumours: a study on 232 dogs. J Comp Pathol. 2008;138(2-3):86–89. doi: 10.1016/j.jcpa.2007.11.002. [DOI] [PubMed] [Google Scholar]
- Haers H, Saunders JH. Review of clinical characteristics and applications of contrast-enhanced ultrasonography in dogs. J Am Vet Med Assoc. 2009;234(4):460–70, 430. doi: 10.2460/javma.234.4.460. [DOI] [PubMed] [Google Scholar]
- Hall WC, Nielsen SW, McEntee K. Tumours of the prostate and penis. Bull World Health Organ. 1976;53(2-3):247–256. [PMC free article] [PubMed] [Google Scholar]
- Johnston GR, Feeney DA, Rivers B, Walter PA. Diagnostic imaging of the male canine reproductive organs. Vet Clin North Am Small Anim Pract. 1991;21(3):553–589. doi: 10.1016/S0195-5616(91)50061-9. [DOI] [PubMed] [Google Scholar]
- Kaneko M, Lenon MSL, Storino Ramacciotti L, Medina LG, Sayegh AS, La Riva A, Perez LC, Ghoreifi A, Lizana M, Jadvar DS, Lebastchi AH, Cacciamani GE, Abreu AL. Multiparametric ultrasound of prostate: role in prostate cancer diagnosis. Ther Adv Urol. 2022;14:17562872221145625. doi: 10.1177/17562872221145625. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Konig HE, Leibich HG. Anatomia dos animais domésticos: texto e atlas colorido. 6. Porto Alegre: Artmed; 2016. [Google Scholar]
- Krook L. A statistical investigation of carcinoma in the dog. Acta Pathol Microbiol Scand. 1954;35(5):407–422. doi: 10.1111/j.1699-0463.1954.tb00886.x. [DOI] [PubMed] [Google Scholar]
- Lévy X, Niżański W, von Heimendahl A, Mimouni P. Diagnosis of common prostatic conditions in dogs: an update. Reprod Domest Anim. 2014;49(Suppl 2):50–57. doi: 10.1111/rda.12296. [DOI] [PubMed] [Google Scholar]
- Liu J-B, Wansaicheong G, Merton DA, Chiou S-Y, Sun Y, Li K, Forsberg F, Edmonds PR, Needleman L, Halpern EJ. Canine prostate: contrast-enhanced us-guided radiofrequency ablation with urethral and neurovascular cooling – initial experience. Radiology. 2008;247(3):717–725. doi: 10.1148/radiol.2473071334. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lucas X, Rodenas C, Cuello C, Gil M, Parrilla I, Soler M, Belda E, Agut A. Unusual systemic metastases of malignant seminoma in a dog. Reprod Domest Anim. 2012;47(4):e59–61. doi: 10.1111/j.1439-0531.2011.01927.x. [DOI] [PubMed] [Google Scholar]
- Mantziaras G. Imaging of the male reproductive tract: not so easy as it looks like. Theriogenology. 2020;150:490–497. doi: 10.1016/j.theriogenology.2020.03.009. [DOI] [PubMed] [Google Scholar]
- Mantziaras G, Luvoni GC. Advanced ultrasound techniques in small animal reproduction imaging. Reprod Domest Anim. 2020;55(Suppl 2):17–25. doi: 10.1111/rda.13587. [DOI] [PubMed] [Google Scholar]
- Mattoon JS, Nyland TG. In: Small animal diagnostic ultrasound. Nyland TG, Mattoon JS, editors. St. Louis: Elsevier; 2002. Prostate and testes. pp. 250–CP1. [DOI] [Google Scholar]
- McEntee MC. Reproductive oncology. Clin Tech Small Anim Pract. 2002;17(3):133–149. doi: 10.1053/svms.2002.34642. [DOI] [PubMed] [Google Scholar]
- Meomartino L, Greco A, Di Giancamillo M, Brunetti A, Gnudi G. Imaging techniques in veterinary medicine. Part I: radiography and ultrasonography. Eur J Radiol Open. 2021;8:100382. doi: 10.1016/j.ejro.2021.100382. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Michels G, Knapp D, David M, Lantz G, Munjar T, Blevins W, DeNicola DB. Penile prolapse and urethral obstruction secondary to lymphosarcoma of the penis in a dog. J Am Anim Hosp Assoc. 2001;37(5):474–477. doi: 10.5326/15473317-37-5-474. [DOI] [PubMed] [Google Scholar]
- Miller MA, Hartnett SE, Ramos-Vara JA. Interstitial cell tumor and sertoli cell tumor in the testis of a cat. Vet Pathol. 2007;44(3):394–397. doi: 10.1354/vp.44-3-394. [DOI] [PubMed] [Google Scholar]
- Mostachio GQ, Apparício M, Vicente WRR, Cardilli DJ, Motheo TF, Toniollo GH. Intraabdominal torsion of a neoplastic testicle and prostatic cyst in a cryptorchid dog. Schweiz Arch Tierheilkd. 2007;149(9):408–412. doi: 10.1024/0036-7281.149.9.408. [DOI] [PubMed] [Google Scholar]
- Ohlerth S, O’Brien RT. Contrast ultrasound: general principles and veterinary clinical applications. Vet J. 2007;174(3):501–512. doi: 10.1016/j.tvjl.2007.02.009. [DOI] [PubMed] [Google Scholar]
- Oliveira MP, Barni BDS, Heinen Schuster LA, Guimarães Gerardi D, Contesini EA, Alievi MM, Paravirini SP. Feline prostatic carcinoma. Acta Sci Vet. 2019;47 doi: 10.22456/1679-9216.98793. [DOI] [Google Scholar]
- Ophir J, Alam SK, Garra BS, Kallel F, Konofagou EE, Krouskop T, Merritt CR, Righetti R, Souchon R, Srinivasan S, Varghese T. Elastography: imaging the elastic properties of soft tissues with ultrasound. J Med Ultrason. 2002;29(4):155–171. doi: 10.1007/BF02480847. [DOI] [PubMed] [Google Scholar]
- Orlandi R, Vallesi E, Boiti C, Polisca A, Bargellini P, Troisi A. Characterization of testicular tumor lesions in dogs by different ultrasound techniques. Animals. 2022;12(2):210. doi: 10.3390/ani12020210. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Palmieri C, Fonseca-Alves CE, Laufer-Amorim R. A review on canine and feline prostate pathology. Front Vet Sci. 2022;9:881232. doi: 10.3389/fvets.2022.881232. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Peppler C, Weissert D, Kappe E, Klump S, Kramer M, Reinacher M, et al. Osteosarcoma of the penile bone (os penis) in a dog. Aust Vet J. 2009;87(1-2):52–55. doi: 10.1111/j.1751-0813.2008.00371.x. [DOI] [PubMed] [Google Scholar]
- Pettina G, Bucci R, Mazzetti A, Quartuccio M, Robbe D, Pisu MC. Contrast-enhanced ultrasound (CEUS) evaluation of canine prostatic hyperplasia before and after osaterone acetate therapy: preliminary results. Animals. 2024;14(11):1683. doi: 10.3390/ani14111683. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pugh CR, Konde LJ. Sonographic evaluation of canine testicular and scrotal abnormalities: a review of 26 case histories. Vet Radiol. 1991;32(5):243–250. doi: 10.1111/j.1740-8261.1991.tb00114.x. [DOI] [Google Scholar]
- Quaia E. Physical basis and principles of action of microbubble-based contrast agents. contrast media in ultrasonography. Berlin: Springer-Verlag; 2005. pp. 15–30. [DOI] [Google Scholar]
- Russo M, England GCW, Catone G, Marino G. Imaging of canine neoplastic reproductive disorders. Animals. 2021;11(5):1213. doi: 10.3390/ani11051213. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sidhu P. Multiparametric ultrasound (MPUS) imaging: terminology describing the many aspects of ultrasonography. Ultraschall Med. 2015;36(4):315–317. doi: 10.1055/s-0035-1553381. [DOI] [PubMed] [Google Scholar]
- Sinagra L, Orlandi R, Caspanello T, Troisi A, Iannelli NM, Vallesi E, Pettina G, Bargellini P, De Majo M, Boiti C, Cristarella S, Quartuccio M, Polisca A. Contrast-enhanced ultrasonography (CEUS) in imaging of the reproductive system in dogs: a literature review. Animals. 2023;13(10):1615. doi: 10.3390/ani13101615. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith J. Canine prostatic disease: a review of anatomy, pathology, diagnosis and treatment. Theriogenology. 2008;70(3):375–383. doi: 10.1016/j.theriogenology.2008.04.039. [DOI] [PubMed] [Google Scholar]
- Spada S, De Felice D, Arlt S, Aires LPN, England GCW, Russo M. Long-term ultrasonographic changes of the canine prostate gland after castration. Front Vet Sci. 2025;11:1524896. doi: 10.3389/fvets.2024.1524896. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stokowski S, Ruth J, Lanz O, Ziglioli V. Computed tomographic features in a case of bilateral neoplastic cryptorchidism with suspected torsion in a dog. Front Vet Sci. 2016;3:33. doi: 10.3389/fvets.2016.00033. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Trappler MC, Popovitch CA, Goldschmidt MH, Goldschmidt KH, Risbon RE. Scrotal tumors in dogs: a retrospective study of 676 cases (1986-2010) Can Vet J. 2014;55(1):1229–1233. [PMC free article] [PubMed] [Google Scholar]
- Trautwein LGC, Hidalgo MMT, Almeida ABM, Haddad J, Na, Cardoso GS, Flaiban KKMC, Silva VW, Silva LAS, Martins MIM. Evaluation of the testicular artery Doppler velocimetry and its correlation with sperm defects in domestic cats. Anim Reprod Sci. 2024;267:107515. doi: 10.1016/j.anireprosci.2024.107515. [DOI] [PubMed] [Google Scholar]
- Troisi A, Orlandi R, Bargellini P, Menchetti L, Borges P, Zelli R, Polisca A. Contrast-enhanced ultrasonographic characteristics of the diseased canine prostate gland. Theriogenology. 2015;84(8):1423–1430. doi: 10.1016/j.theriogenology.2015.07.029. [DOI] [PubMed] [Google Scholar]
- Vignoli M, Russo M, Catone G, Rossi F, Attanasi G, Terragni R, Saunders J, England G. Assessment of Vascular Perfusion Kinetics Using Contrast‐enhanced Ultrasound for the Diagnosis of Prostatic Disease in Dogs. Reprod Domest Anim. 2011;46(2):209–213. doi: 10.1111/j.1439-0531.2010.01629.x. [DOI] [PubMed] [Google Scholar]
- Volta A, Manfredi S, Vignoli M, Russo M, England G, Rossi F, Bigliardi E, Di Ianni F, Parmigiani E, Bresciani C, Gnudi G. Use of contrast‐enhanced ultrasonography in chronic pathologic canine testes. Reprod Domest Anim. 2014;49(2):202–209. doi: 10.1111/rda.12250. [DOI] [PubMed] [Google Scholar]
- Yates D, Hayes G, Heffernan M, Beynon R. Incidence of cryptorchidism in dogs and cats. Vet Rec. 2003;152(16):502–504. doi: 10.1136/vr.152.16.502. [DOI] [PubMed] [Google Scholar]
- Zappone V, Iannelli NM, Sinagra L, Donato G, Quartuccio M, Cristarella S, De Majo M, Caspanello T. Assessment of testicular stiffness in fertile dogs with shear wave elastography techniques: a pilot study. Front Vet Sci. 2024;11:1397347. doi: 10.3389/fvets.2024.1397347. [DOI] [PMC free article] [PubMed] [Google Scholar]
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