Editorial Type: Case Reports
 | 
Online Publication Date: 01 Sept 2016

Seminal Vesiculitis in Three Pet Rabbits (Oryctolagus cuniculus)

LV (veterinarian),
LV (veterinarian),
LV (veterinarian),
LV (veterinarian), and
LV (veterinarian), MSc
Article Category: Case Report
Page Range: 335 – 340
DOI: 10.5326/JAAHA-MS-6368
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ABSTRACT

To date, descriptions of pathologic conditions of the seminal vesicle in rabbits are scarce and limited to the laboratory animals in experimental conditions. The present article describes three cases of strangury, abdominal pain, and anorexia associated with seminal vesiculitis in pet rabbits. Three non-neutered male pet rabbits aged 3.6, 1.5, and 2.1 yrs were presented with strangury, abdominal pain, and anorexia. Seminal vesiculitis was diagnosed based on clinical signs and ultrasonography findings. Vesiculectomy was performed in two cases that presented strangury refractory to medical treatment, and diagnosis was confirmed by histopathology. In the third case, the patient received medical treatment, and a sequela in the form of lithiasis of the seminal vesicle was detected 3 yrs later. Plain radiographs were nearly unremarkable, and results from complete blood analysis and urinalysis were not specific in all three cases. Contrast radiography was performed in one case, showing a dilated seminal vesicle. Ultrasound and surgical biopsy seem to be the most sensitive techniques in the diagnosis of this pathology. Seminal vesiculitis must be included in the differential diagnosis of acute or chronic strangury in male pet rabbits.

Introduction

Seminal vesiculitis is the inflammation of a seminal vesicle. Local congestion of the seminal vesicles or prostate, infections (chlamydial, mycoplasmal, bacterial, fungal, or viral), parasites, and non-infectious inflammation can cause seminal vesiculitis.1 In human males, seminal vesiculitis most frequently arises secondary to prostatitis, orchitis, epididymitis, cystitis, urethritis, or proctitis.1

In veterinary medicine, seminal vesiculitis is widely reported in horses, ruminants, and rodents, and conceivably can affect other species in which seminal vesicles are present.24 In rabbits, descriptions of pathologic conditions of the seminal vesicle are scarce and limited to the laboratory rabbits in experimental conditions.5,6 To the knowledge of the authors, no cases of seminal vesiculitis have been reported in pet rabbits.

Unlike human males, bulls, or stallions, which have paired seminal vesicles, male domestic rabbits (Oryctolagus cuniculus) have an unpaired seminal vesicle that is a part of the so-called prostatic complex.68 Different terms, such as glandula vesicularis, glandula seminalis, and vesicula seminalis have been used by different authors.6,8,9 In this article, the term seminal vesicle, according to Zwicker (1985), is used.

The present article describes three cases of strangury, abdominal pain, and anorexia associated with seminal vesiculitis in non-neutered male pet rabbits.

Case Report

Three non-neutered male pet rabbits (Patient 1, Patient 2, and Patient 3) were presented with strangury on different occasions to a veterinary center. The age and the weight of the patients were 3.6, 1.5, and 2.1 yrs and 2.32, 2.05, and 1.74 kg, respectively. In all three cases, radiographic and ultrasonographic examinations, urinalysis, and complete blood analysis were performed. Blood analysis included hematology, blood chemistry, and protein electrophoresis.

Patient 1

Patient 1 presented for a three-day duration history of anorexia and apathy. Physical examination revealed severe dehydration, apathy, painful abdominal palpation, and empty urinary bladder. Hematology and protein electrophoresis were unremarkable. Blood chemistry showed hyperglycemia (183 mg/dl; reference range [RR] 74–148 mg/dl) and hypertriglyceridemia (225 mg/dl; RR 50–200 mg/dl).10,11 Radiography showed signs of digestive hypomotility but was otherwise unremarkable. The rabbit was hospitalized, and strangury and vesical tenesmus were noted by attending staff. Urine was collected by urinary catheterization. Urinalysis revealed a urine specific gravity (USG) of 1.036 (RR 1.003–1.060), pH of 5 (RR 7.6–8.8), traces of blood and proteins, and scarce granular casts.11,12 Ultrasound examination revealed a distended seminal vesicle protruding into the abdominal cavity and compressing the proximal urethra. The content was hypoechoic with multiple hyperechoic foci. The seminal vesicle measured 13.7 mm (RR 5.4–5.6 mm) in width, 5.7 mm (RR 4.5–4.6 mm) in depth, and at least 30.0 mm (RR 6.2–6.3 mm) in length (caudal limit was not clearly identified).13 Proprostate measured 17.7 mm (RR 10.7–16.7 mm) in width, 8.8 mm (RR 4.3–7.5 mm) in depth, and at least 17.8 mm (RR 6.4–19.8 mm) in length (caudal limit was not clearly identified), and had otherwise normal echographic appearance (Figure 1A).8 No clinical signs of cystitis or other pathologies that would explain the strangury were observed. Particularly, no inflammatory or epithelial cells were found in urine, as would be expected in case of cystitis or urethritis. Consequently, prostatic complex pathology was suspected, and presumptive diagnosis of proprostatitis and seminal vesiculitis with secondary strangury was established based on proprostate enlargement and abnormal seminal vesicle contents and size. Patient 1 was treated with marbofloxacina (5 mg/kg SC q 24 hr), hyoscine butylbromide (1 mg/kg SC q 8 hr) in combination with sodium metamizoleb (125 mg/kg SC q 8 hr), buprenorphinec (0.05 mg/kg SC q 8 hr), ranitidined (4 mg/kg SC q 8 hr), metoclopramidee (0.5 mg/kg SC q 8 hr), and intravenous fluid therapy.14 After 5 days, no significant improvement in strangury and vesical tenesmus was observed. Despite normalization of the hydration status and analgesic treatment, the rabbit remained apathetic, anorexic, and with signs of abdominal pain. Ultrasound follow-up examinations showed no changes in size or contents of the seminal vesicle. Because of the lack of improvement, laparotomy was performed, revealing a distended and congested seminal vesicle filled with whitish, thick fluid (Figure 1B). The fluid was aspirated using a 1 cc syringe and 25G needle (Figure 1C). Cytology of the fluid revealed inflammatory cells (mainly neutrophils) and gram-positive cocci. A sample for microbiological culture was submitted and later resulted in a pure culture of multidrug-resistant Staphylococcus sp. The seminal vesicle was incised and flushed with sterile saline. Vesiculectomy and bilateral orchiectomy were performed. A combination of benzylpenicillin G (80,000 UI/kg) and dihydrostreptomycin sulphatef (100 mg/kg SC q 24 hr) were added to the treatment after the surgery. Patient 1 recovered uneventfully from the surgery and started eating the same day. This rabbit was discharged 2 wk later and had no recurrences for 11 mo.

Figure 1. A: Ultrasonographic image from Patient 1 in sagittal plane showing the dilated seminal vesicle (arrows) with hypoechoic contents. The urinary bladder (UB), the rectum (REC), and the proprostate measuring 0.88 cm in depth are identifiable. B: A congested seminal vesicle (arrowhead) dilated with purulent contents and protruding into the abdominal cavity dorsally to the urinary bladder (UB) neck was evident during laparotomy (Patient 1) C: Aspiration of seminal vesicle contents during surgery (Patient 1) D: Ultrasonographic image from Patient 2 in transverse plane (TRANS) showing a severely dilated seminal vesicle (SV) dorsolateral to the urinary bladder (UB) displaced to the left and ventrolateral to the rectum (REC).Figure 1. A: Ultrasonographic image from Patient 1 in sagittal plane showing the dilated seminal vesicle (arrows) with hypoechoic contents. The urinary bladder (UB), the rectum (REC), and the proprostate measuring 0.88 cm in depth are identifiable. B: A congested seminal vesicle (arrowhead) dilated with purulent contents and protruding into the abdominal cavity dorsally to the urinary bladder (UB) neck was evident during laparotomy (Patient 1) C: Aspiration of seminal vesicle contents during surgery (Patient 1) D: Ultrasonographic image from Patient 2 in transverse plane (TRANS) showing a severely dilated seminal vesicle (SV) dorsolateral to the urinary bladder (UB) displaced to the left and ventrolateral to the rectum (REC).Figure 1. A: Ultrasonographic image from Patient 1 in sagittal plane showing the dilated seminal vesicle (arrows) with hypoechoic contents. The urinary bladder (UB), the rectum (REC), and the proprostate measuring 0.88 cm in depth are identifiable. B: A congested seminal vesicle (arrowhead) dilated with purulent contents and protruding into the abdominal cavity dorsally to the urinary bladder (UB) neck was evident during laparotomy (Patient 1) C: Aspiration of seminal vesicle contents during surgery (Patient 1) D: Ultrasonographic image from Patient 2 in transverse plane (TRANS) showing a severely dilated seminal vesicle (SV) dorsolateral to the urinary bladder (UB) displaced to the left and ventrolateral to the rectum (REC).
Figure 1 A: Ultrasonographic image from Patient 1 in sagittal plane showing the dilated seminal vesicle (arrows) with hypoechoic contents. The urinary bladder (UB), the rectum (REC), and the proprostate measuring 0.88 cm in depth are identifiable. B: A congested seminal vesicle (arrowhead) dilated with purulent contents and protruding into the abdominal cavity dorsally to the urinary bladder (UB) neck was evident during laparotomy (Patient 1) C: Aspiration of seminal vesicle contents during surgery (Patient 1) D: Ultrasonographic image from Patient 2 in transverse plane (TRANS) showing a severely dilated seminal vesicle (SV) dorsolateral to the urinary bladder (UB) displaced to the left and ventrolateral to the rectum (REC).

Citation: Journal of the American Animal Hospital Association 52, 5; 10.5326/JAAHA-MS-6368

Histopathology of the seminal vesicle showed mild neutrophilic adenitis. Both testicles were histologically normal.

Patient 2

Patient 2 was presented with chronic pollakiuria. Owners reported a 6- to 7-mo history of strong urine smell, the rabbit's perianal and inguinal region being permanently wet, and several days of anorexia and apathy. Physical examination revealed severe dehydration, apathy, poor body condition, dermatitis of the perianal and inguinal regions, bilateral hind limbs pododermatitis and lameness, painful abdominal palpation, and distended urinary bladder (despite dehydration). Hematology revealed slight leucocytosis (11500 WBC/mcl; RR 5100–9700 WBC/mcl) with left shift (6% of band neutrophils; RR 0%–1%).10,15 Protein electrophoresis showed normal total proteins (68 g/l; RR 55–72 g/l) with beta- (12.0 g/l and 17.6%; RR 9.5–11.5 g/l, 8.0%–14.8%) and relative gamma-globulinemia (7.7 g/l and 11.3%; RR 5.7–7.7 g/l, 8.6%–9.6%).16,17 These results are consistent with chronic inflammation with infection as a most probable cause.1619 Infection by Encephalitozoon cuniculi was considered unlikely, since this patient presented undetectable immunoglobulin G titers (<1/80) against this microorganism 9 mo earlier and had no contact with other rabbits or rodents.17 Radiography revealed increased radiodensity in the caudal abdomen, an abnormal shape of the urinary bladder, and signs of digestive hypomotility. Urine was collected by cystocentesis. Urinalysis revealed a USG of 1.012 (RR 1.003–1.060), pH 8.0 (RR 7.6–8.8), moderate hematuria, pyuria and sporadic transition, and squamous epithelial cells.11 Ultrasound examination revealed a noticeably enlarged seminal vesicle with hypoechoic content, thickening of the urinary bladder mucosa, and constriction of urinary bladder at the mid region (Figure 1D). The urinary bladder was displaced ventrally and laterally to the left by the dilated seminal vesicle. The seminal vesicle measured 15.7 mm (RR 5.4–5.6 mm) in width, 16.7 mm (RR 4.5–4.6 mm) in depth, and at least 34.6 mm (RR 6.2–6.3 mm) in length.13 Proprostate measured 10.7 mm (RR 10.7-16.7 mm) in width, 8.4 mm (RR 4.3-7.5 mm) in depth and 11.5 mm (RR 6.4-19.8 mm) in length.8 Contrast radiography was performed instilling 10 ml iohexol 300 mg I/ml solutiong through a tomcat catheter in the urethra. Radiography confirmed urinary bladder stricture and revealed unintentional placement of the urinary catheter in the seminal vesicle (Figure 2A, B). After injection of the contrast media, the maximum radiographic measurements of the seminal vesicle were 23 mm in width, 18 mm in depth and 46 mm in length.

Figure 2. A: Contrast radiograph from Patient 2 in dorsoventral projection. Seminal vesicle full of contrast media is visible on the right (left side of the patient). Urinary bladder is on the left (right side of the patient). B: Contrast radiograph from Patient 2 in lateral projection. Seminal vesicle full of contrast media is positioned dorsally to the urinary bladder that presents a stricture. C: Ultrasonographic image from Patient 3 showing the calculus inside one of the lobules of the seminal vesicle (arrow) projecting an acoustic shadow. The seminal vesicle is not dilated but the dorsal wall is identifiable (arrowheads). The rectum is no visible on this image. D: Radiograph from Patient 3 in lateral projection showing a single calculus located in the seminal vesicle.Figure 2. A: Contrast radiograph from Patient 2 in dorsoventral projection. Seminal vesicle full of contrast media is visible on the right (left side of the patient). Urinary bladder is on the left (right side of the patient). B: Contrast radiograph from Patient 2 in lateral projection. Seminal vesicle full of contrast media is positioned dorsally to the urinary bladder that presents a stricture. C: Ultrasonographic image from Patient 3 showing the calculus inside one of the lobules of the seminal vesicle (arrow) projecting an acoustic shadow. The seminal vesicle is not dilated but the dorsal wall is identifiable (arrowheads). The rectum is no visible on this image. D: Radiograph from Patient 3 in lateral projection showing a single calculus located in the seminal vesicle.Figure 2. A: Contrast radiograph from Patient 2 in dorsoventral projection. Seminal vesicle full of contrast media is visible on the right (left side of the patient). Urinary bladder is on the left (right side of the patient). B: Contrast radiograph from Patient 2 in lateral projection. Seminal vesicle full of contrast media is positioned dorsally to the urinary bladder that presents a stricture. C: Ultrasonographic image from Patient 3 showing the calculus inside one of the lobules of the seminal vesicle (arrow) projecting an acoustic shadow. The seminal vesicle is not dilated but the dorsal wall is identifiable (arrowheads). The rectum is no visible on this image. D: Radiograph from Patient 3 in lateral projection showing a single calculus located in the seminal vesicle.
Figure 2 A: Contrast radiograph from Patient 2 in dorsoventral projection. Seminal vesicle full of contrast media is visible on the right (left side of the patient). Urinary bladder is on the left (right side of the patient). B: Contrast radiograph from Patient 2 in lateral projection. Seminal vesicle full of contrast media is positioned dorsally to the urinary bladder that presents a stricture. C: Ultrasonographic image from Patient 3 showing the calculus inside one of the lobules of the seminal vesicle (arrow) projecting an acoustic shadow. The seminal vesicle is not dilated but the dorsal wall is identifiable (arrowheads). The rectum is no visible on this image. D: Radiograph from Patient 3 in lateral projection showing a single calculus located in the seminal vesicle.

Citation: Journal of the American Animal Hospital Association 52, 5; 10.5326/JAAHA-MS-6368

Diagnosis of cystitis and seminal vesiculitis was made. Patient 2 was hospitalized and treated with marbofloxacina (5 mg/kg SC q 24 hr), hyoscine butylbromide (1 mg/kg SC q 8 hr) in combination with sodium metamizoleb (125 mg/kg SC q 8 hr), fentanylh 12.5 mcg/h transdermal patch, intravenous fluid therapy and symptomatic treatment for digestive hypomotility for 4 days. The patient showed normalization of hydration status and general improvement, but the strangury persisted. Vesiculectomy, a biopsy of the urinary bladder, and bilateral orchiectomy were performed on day 4. Patient 2 recovered without incidence and was discharged after 7 days. This rabbit had no recurrences for 8 mo, and pollakiuria, strangury and urine scalding resolved completely.

Histopathology of the seminal vesicle showed mild acute multifocal erosive adenitis with multifocal hemorrhage and mucosal atrophy. Possible discrete hypertrophy of the muscular layer was also observed. The urinary bladder mucosa and the superficial part of the muscular layer presented occasional foci of hemorrhage associated to edema of the mucosa. Both testicles presented moderate atrophy of seminal tubules.

Patient 3

Patient 3 was presented with acute anorexia, priapism, and hematuria. During the anamnesis, the owners reported a history of chronic difficulty in urination. Physical examination revealed mild dehydration, painful abdominal palpation, and a moderately dilated urinary bladder. Complete blood analysis showed no remarkable findings, except for the pronounced hyperglycemia (339 mg/dl; RR 74–148 mg/dl).10,11 Urine was collected by manual extrusion of the urinary bladder. Urinalysis revealed transparent mucus in urine, a USG of 1.008 (RR 1.003–1.060), pH of 7.5 (RR 7.6–8.8), traces of blood and proteins, and occasional squamous epithelial cells.11 Radiography revealed a moderate amount of sludge in the urinary bladder and was unremarkable otherwise. Ultrasound examination revealed a distended seminal vesicle with hypoechoic contents protruding into the abdominal cavity. The seminal vesicle measured 13.3 mm (RR 5.4–5.6 mm) in width, 7.3 mm (RR 4.5–4.6 mm) in depth, and at least 23.0 mm (RR 6.2–6.3 mm) in length.13 Proprostate measured 13.8 mm (RR 10.7–16.7 mm) in width, 8.8 mm (RR 4.3–7.5 mm) in depth, and 17.6 mm (RR 6.4–19.8 mm) in length, and prostate measured 7.2 mm (RR 3.2–7.8 mm) in depth and 14.1 mm (RR 8.4–15.2 mm) in width.8 Proprostate and prostate had normal ultrasonographic appearance. The urinary bladder did not present ultrasonography signs of cystitis. Prostatic complex pathology was suspected based on clinical signs, the absence of signs of cystitis, and abnormal contents of the seminal vesicle and proprostate enlargement detected ultrasonographically. A presumptive diagnosis of seminal vesiculitis and proprostatitis was made, and the patient was treated with a single injection of buprenorphine at 0.05 mg/kg SC, trimethoprim/sulfamethoxazolei (40 mg/kg PO q 12 hr), and meloxicamj (0.3 mg/kg PO q 12 hr) for 7 days.14

After initial improvement and complete resolution of the clinical signs, Patient 3 relapsed 1 month after discharge with identical clinical signs and findings. Complete blood analysis was again unremarkable except for marked hyperglycemia (399 mg/dl; RR 74–148 mg/dl).10,11 Ultrasound revealed hypoechoic content and hyperechoic wall of the seminal vesicle, prostate measurements of 8.8 mm (RR 3.5–7.9 mm) in depth and 15.3 mm (RR 8.4-–5.2 mm) in width. Proprostate and urinary bladder had normal ultrasonographic appearance. Urinalysis revealed few inflammatory cells in this occasion. The patient was treated with trimethoprim/sulfamethoxazole and meloxicam with the same protocol and improved noticeably in 24 hrs. Bilateral orchiectomy was performed 4 days later. The rabbit recovered uneventfully and did not present recurrences for 3 years. However, the owners reported lately that a slight difficulty in urination persisted.

Patient 3 showed three more episodes of exacerbated strangury in 4 yrs. The owners reported that the animal was repeatedly adopting posture to urinate without voiding urine and was anorexic and apathetic. Clinical and laboratory findings were similar to the previously described, but radiography and ultrasound revealed lithiasis and hyperechogenicity of the wall of the seminal vesicle (Figure 2C, D). Ultrasonographic appearance of the prostate was normal in these occasions. Only in one occasion, fever (rectal temperature 40.5°C; RR 38.5°C–40°C), abnormal urinalysis findings (presence of significant amount of transition epithelium cells, leucocytes and erythrocytes in urinary sediment), and ultrasonographically detected slight hypertrophy of urinary bladder mucosa were interpreted as signs of cystitis concurrent to vesicle lithiasis.14 The rabbit was treated with meloxicamj (0.3 mg/kg PO q 12 hr) and presented rapid improvement in all occasions. Cystitis was treated with marbofloxacink (5 mg/kg PO q 24 hr) for 7 days. Surgical treatment of seminal vesicle lithiasis was rejected by the owners.

Discussion

Seminal vesiculitis must be included in the differential diagnosis of acute or chronic strangury in male pet rabbits. Based on the results obtained from the three patients described in this article and the previously published data, the etiopathogenesis of the seminal vesiculitis in rabbits can involve concomitant inflammatory, endocrine, and toxic pathologic processes, similar to what occurs in other species.16,20

The size of seminal vesicles is difficult to interpret due to scarce scientific data. According to Del Sol and Vasquez (2003), seminal vesicles from 12 mixed-breed rabbits measured an average maximum of 23.6 mm in length and 13.7 mm in width. Dimitrov et al. (2011) reported seminal vesicle dimension ranges of 6.2–6.3 mm in length, 5.4–5.6 mm in width, and 4.5–4.6 mm in depth, measured by computed tomography in eight adult New Zealand White rabbits weighing between 2.8 and 3.2 kg. However, according to Holtz and Foote (1978), the seminal vesicle (called vesicular gland) is variable in size and can contain an inconstant amount of clear or slightly turbid liquid. The measurements of the seminal vesicle in 17 adult Dutch-belted rabbits weighing around 2 kg were reported as high as 38 mm in length, 19 mm in width, and 14.4 mm in depth. The article, however, does not report any kind of analysis of the content or the walls of the apparently dilated vesicles in order to determine whether they were actually normal. High incidence of subclinical pathology of seminal vesicles was reported in Dutch-belted rabbits by Zwicker et al. (1995). In the three clinical cases described in this article, the seminal vesicles presented changes in the wall and content echogenicity. They were also perceptibly enlarged compared to the data by Del Sol and Vasquez (2003) and Dimitrov et al, (2011), but only Patient 2 presented dilation of seminal vesicles compared to data by Holtz and Foote (1978).

The seminal vesicle is located dorsally to the urinary bladder neck and the pelvic urethra and ventrally to the rectum at the level of the S1 vertebra.13 It is the authors' experience that seminal vesicles in pet rabbits without clinical signs of urologic pathology are only slightly protruding, if at all, into the abdominal cavity and are slightly distended with anechoic fluid. The wall of the seminal vesicle is thin and its echogenicity is similar to the surrounding tissues. In some individuals, the seminal vesicle is not even evident ultrasonographically. Consequently, a noticeably distended seminal vesicle with hypo- or hyperechoic contents, especially in the presence of strangury, can be interpreted as a sign of seminal vesiculitis with a probable additional inflammatory process in the pelvic region.

Radiology, hematology, blood chemistry, and urinalysis seem to be of limited value. The urinalysis results from the three patients described in this article suggest that pyuria and hematuria are not consistently found, even in cases of important amounts of purulent contents inside the seminal vesicle. Semen examination could be important in the diagnosis of seminal vesiculitis, as it is in ruminants and stallions.2,3 However, semen collection is not a common procedure with pet rabbits. Ultrasound and surgical biopsy seem to be the most sensitive techniques in the diagnosis of this pathology. In Patient 3, not treated surgically, histologic evaluation of the seminal vesicle was not performed. The presumptive diagnosis of seminal vesiculitis is supported by ultrasonography findings and the eventual stone formation. In human medicine, lithiasis of the seminal vesicles is rare and etiologically related to pathological processes of the male urogenital tract, such as ectopic ureter, seminal vesicle cysts, seminal stasis, inflammation of adjacent tissues, and infection.21,22 Seminal lithiasis in Patient 3 was associated with what appeared to be a recurrent non-infectious inflammatory vesiculitis with secondary strangury responsive to treatment with meloxicam.

Treatment of seminal vesiculitis in different species commonly involves antimicrobials, anti-inflammatory and analgesic drugs, and sometimes vesiculectomy.3,23,24 The rapid improvement after vesiculectomy in patients 1 and 2 suggest that the strangury was due to the enlargement of the seminal vesicle and compression of the urethra. Medical treatment of seminal vesiculitis seldom cures, but it frequently causes a remission, and a post-infectious inflammatory vesiculitis is a common sequela.3,25 Intravesicular injection of antibiotic drugs was described in the bull as an alternative to systemic antibiotic treatment.26

Conclusion

In veterinary practice, a common recommendation for prevention and treatment of the male accessory genital glands pathology is castration when the reproductive potential of the individual is not an issue.27 However, it is worth reminding that this recommendation is focused mostly on domestic carnivores that lack seminal vesicles. The accessory genital glands of the male rabbits are sensitive to sexual hormones, and the androgens have a stimulatory effect on the glandular activity.28 The effectiveness of neutering in prevention of seminal vesiculitis in rabbits is unknown.

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Footnotes

  1. Marbocyl 2%; Vetoquinol E.V.S.A., Madrid, Spain

  2. Buscapina compositum; Boehringer Ingelheim, S.A., Ingelheim, Germany

  3. Buprex; Schering Plough, S.A., Kenilworth, NJ

  4. Ranitidina Normon EFG amp. 50mg/5ml; Normon S.A., Madrid, Spain

  5. Primepran sol. iny. 10 mg/2ml; Sanofi S.A., Gentilly, France

  6. Duphapen Strep; Fort Dodge Veterinaria, S.A., Girona, Spain

  7. Omnipaque; GE Healthcare, Chicago, IL

  8. Durogesic Matrix 12; Janssen, S.A., Beerse, Belgium

  9. Septrin; UCB Pharma, S.A., Brussels, Belgium

  10. Metacam suspension oral 1.5 mg/ml; Boerhinger Ingelheim, S.A., Ingelheim, Germany

  11. Marbocyl P 5mg; Vetoquinol E.V.S.A., Madrid, Spain

  12. RR (reference range) USG (urine specific gravity)
Copyright: © 2016 by American Animal Hospital Association 2016
Figure 1
Figure 1

A: Ultrasonographic image from Patient 1 in sagittal plane showing the dilated seminal vesicle (arrows) with hypoechoic contents. The urinary bladder (UB), the rectum (REC), and the proprostate measuring 0.88 cm in depth are identifiable. B: A congested seminal vesicle (arrowhead) dilated with purulent contents and protruding into the abdominal cavity dorsally to the urinary bladder (UB) neck was evident during laparotomy (Patient 1) C: Aspiration of seminal vesicle contents during surgery (Patient 1) D: Ultrasonographic image from Patient 2 in transverse plane (TRANS) showing a severely dilated seminal vesicle (SV) dorsolateral to the urinary bladder (UB) displaced to the left and ventrolateral to the rectum (REC).


Figure 2
Figure 2

A: Contrast radiograph from Patient 2 in dorsoventral projection. Seminal vesicle full of contrast media is visible on the right (left side of the patient). Urinary bladder is on the left (right side of the patient). B: Contrast radiograph from Patient 2 in lateral projection. Seminal vesicle full of contrast media is positioned dorsally to the urinary bladder that presents a stricture. C: Ultrasonographic image from Patient 3 showing the calculus inside one of the lobules of the seminal vesicle (arrow) projecting an acoustic shadow. The seminal vesicle is not dilated but the dorsal wall is identifiable (arrowheads). The rectum is no visible on this image. D: Radiograph from Patient 3 in lateral projection showing a single calculus located in the seminal vesicle.


Contributor Notes

Correspondence: amcasica@telefonica.net (M.A.)
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