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Journal of Veterinary Science and Animal Husbandry

ISSN: 2348-9790

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Ascites Secondary to Compression of the Caudal Vena Cava by Liver Abscesses in a Cow

Received Date: October 29, 2015 Accepted Date: January 19, 2016 Published Date: January 20, 2016

Copyright: © 2016 Braun U. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Abstract

Background: Ascites due to thrombosis of the caudal vena cava is relatively seldom in cattle. To our knowledge, there have been no reports of ascites secondary to compression of the caudal vena cava by liver abscesses. This case report describes the findings in a 3.7-year-old Brown Swiss cow with this disease.

Case presentation: The cow had a distended, pear-shaped abdomen. Ultrasonography of the abdomen showed a massive accumulation of hypoechoic fluid and dilatation of the caudal vena cava. A tentative diagnosis of thrombosis of the caudal vena cava was made, and because of a poor prognosis, the cow was slaughtered. Incision of the abdominal wall released approximately 100 litres of yellow, clear, non-malodorous fluid from the peritoneal cavity. The liver was markedly enlarged, and two abscesses, approximately 10 cm in diameter, were situated immediately adjacent to the caudal vena cava causing compression of the vein. No microbiology culture was done. The final diagnosis was ascites secondary to compression of the caudal vena cava by two liver abscesses and secondary hepatic fibrosis.

Conclusion: This report suggests that compression of the caudal vena cava by liver abscesses should be included in the list of differential diagnosis of conditions associated with ascites and dilatation of the caudal vena in cattle.

Keywords: Cattle; Ascites; Liver abscess; Caudal vena cava; Compression

Background

Ascites is excessive accumulation of fluid in the peritoneal cavity. The ascites fluid can be characterised as inflammatory, non-inflammatory, chylous, urine-like, haemorrhagic or bilious [1]. In cattle, ascites fluid is usually non-inflammatory and associated with vascular congestion due to chronic right-sided heart failure, a mediastinal mass, chronic liver or kidney disease, ileus of the small intestines, enteropathies, peritoneal tumours or thrombosis of the caudal vena cava [1]. There are several reports on ascites associated with thrombosis of the caudal vena cava in cattle [2-5], but to the authors‘ knowledge, there are no reports on ascites secondary to compression of this vein. This case report describes the clinical, ultrasonographic and pathological findings in a 3.7-year-old Brown Swiss cow, which was five months pregnant and had ascites secondary to compression of the caudal vena cava by liver abscesses.

Case presentation

For several days before referral to our clinic, the cow had a marked decrease in appetite and faecal output and progressive distension of the abdomen. On admission, the cow was in poor general health, had a marked decrease in appetite and a pear-shaped abdomen (Figure 1). The rectal temperature was 38.5 oC, the heart rate 68 bpm and the respiratory rate 28 breaths per min. Rumen motility was severely decreased, the rumen was relatively full and there was no distinct layering of rumen contents. Tests for reticular foreign bodies and swinging and percussion auscultation on both sides of the abdomen were negative. Intestinal motility was markedly decreased, and the cow passed small amounts of dark, watery, malodorous faeces. The results of a urine test strip (Combur9-Test, Roche, Basel) were unremarkable. An increased volume of peritoneal fluid was suspected based on sloshing felt during transrectal palpation.

The results of haematological and serum biochemical analyses showed haemoconcentration, increase in γ-GT activity, azotaemia, hypocalcaemia and metabolic acidosis (Table 1).

Transcutaneous ultrasonography was performed using a 5.0 MHz convex transducer. It showed a massive amount of hypoechoic fluid in the peritoneal cavity, and the reticulum (Figure 2), intestines (Figure 3) and liver (Figure 4) were displaced dorsally by the ascites fluid. The liver parenchyma appeared heterogeneous and hyperdense on ultrasonograms. The caudal vena cava was circular and dilated in cross-section (Figure 5) and did not have a normal triangular shape [6]. The gallbladder wall was thicker than normal because of oedema (Figure 4). Ultrasound-guided abdominocentesis yielded yellow, clear, non-malodorous fluid with a specific gravity of 1.034 (reference interval < 1.015), a protein concentration of 46 g/l (reference interval < 30 g/l), urea concentration of 7.5 mmol/l (reference interval similar to that of blood) and creatinine concentration of 94.3 μmol/l (reference interval similar to that of blood). Cytological evaluation of the abdominal fluid showed a few erythrocytes, leukocytes and macrophages, and was classified as a modified transudate. Based on all the findings, a tentative diagnosis of non-inflammatory ascites secondary to thrombosis of the caudal vena cava was made. The cow was slaughtered because of a poor prognosis, and a postmortem examination was carried out. Approximately 100 litres of clear, non-malodorous fluid escaped from the abdomen when the abdominal wall was incised (Figure 6). The liver was markedly increased in size and firmer than normal and had a bumpy surface. Two abscesses with a diameter of approximately 10 cm were located immediately adjacent to the caudal vena cava and compressed it (Figure 7,8). There was no thrombus in the caudal vena cava (Figure 9). Histopathology of the liver parenchyma revealed a diffuse fibrosis, which was especially severe around the centrolobular veins and was often forming fibrous bridges between the periportal spaces (bridging fibrosis). Hepatocytes and hepatic lobules were severely atrophic and midzonal sinusoids were heavily congested and dilated (severe hepatic chronic congestion). Portal tracts were characterized by severe bile duct proliferation and multiplication of arterioles. Several vessel walls were moderately thickend and centrolobular veins were often dilated. The final diagnosis was ascites attributable to compression of the caudal vena cava by two liver abscesses and secondary hepatic fibrosis.

The causes of ascites and the diagnostic work-up of cattle with ascites were recently described in detail [1]. Ultrasonography, abdominocentesis and examination of peritoneal fluid are critical components for determining the aetiology of the problem. Inflammatory and non-inflammatory conditions can be differentiated by peritoneal fluid analysis. Uroperitoneum is diagnosed when the creatinine concentration of peritoneal fluid is higher than that of serum, and an increased concentration of bilirubin in peritoneal fluid usually indicates bile peritonitis. Rupture of a tumour or blood vessel results in haemorrhagic peritoneal fluid, and peritoneal fluid that appears milky and has a high lymphocyte count may indicate chyloabdomen. The most important finding in this case study, other than the massive accumulation of peritoneal fluid, was the change in shape of the caudal vena cava in cross-section. The caudal vena cava normally appears triangular in cross-section [6], but becomes oval to circular with congestion of the vein. Changes in the shape of the vein are of greater diagnostic importance than an increase in the diameter of the vein [7]. Congestion of the caudal vena cava occurs with right-sided heart failure and with obstruction or compression of the vein. In cattle with right-sided heart failure, there is also congestion of the jugular veins, which did not occur in the present case. Our tentative diagnosis of thrombosis of the caudal vena cava appeared to be the most plausible cause because it occurs relatively often in cattle [2-4,7-9]. However, in these cases, a thrombus can rarely be seen via ultrasonography [8-10] because most are located in the part of the caudal vena cava that is obscured by the lungs. An outstanding yet time-consuming method for identifying a thrombus in the caudal vena cava is intraabdominal ultrasonography of the vein through a right-flank laparotomy [11]. Our tentative diagnosis was proved incorrect during postmortem examination, which revealed compression of the caudal vena cava by two liver abscesses. Unfortunately, ultrasonography could not be used to visualize the abscesses because they were located in a part of the liver obscured by the lungs. It is highly likely that a correct diagnosis would have been possible using intraabdominal ultrasonography [11]. The liver abscesses were immediately adjacent to the caudal vena cava and thus led to compression and subsequent congestion of the vein. Liver abscesses are the most common cause of thrombosis of the caudal vena cava in cattle [12-18] and, similar to our case, are situated immediately adjacent to the vein. However, liver abscesses usually rupture into the caudal vena cava and form a fibrinous thrombus attached to the intima, which partially or completely obstructs the lumen of the vein. This did not occur in our case.

Severe ascites usually is a sequel to increased hydrostatic and decreased oncotic pressure. In the case described in this report, increased hydrostatic pressure in the caudal vena cava was caused by an abscess that compressed the vein and impaired blood flow to the heart, and the decreased oncotic pressure was the result of liver fibrosis caused by congestion.

Conclusion

In conclusion, the change in the cross-sectional shape of the caudal vena cava from triangular to circular or oval on ultrasonography and the features found through the necropsy suggest that the ascites was caused by compression performed by the abscess and the secondary hepatic fibrosis.

Author’s contributions

Ueli Braun prepared the manuscript and supervised the clinical and ultrasonographic examination, Manuela Stettler and Stephanie Schramm examined the heifer, postmortem examination was performed by Monika Hilbe. All authors have read and approved the manuscript.

Acknowledgements

The authors thank Dr Rainer Nussbaumer for referring the cow to our clinic, the technicians of the Medical Laboratory for the haematological and biochemical analyses and the animal assistants for looking after the cow.

1 Braun U (2016) Ascites in cattle – Ultrasonographic findings and diagnosis. Vet Clin North Am Food Anim Pract. 32: In press.
13 Stöber M (1966) Pyogene Thrombosen der Vena cava caudalis beim Rind [Pyogenic thrombosis of the inferior vena cava in cattle]. Schweiz Arch Tierheilk 108: 613-21.

JOURNAL OF VETERINARY SCIENCE & ANIMAL HUSBANDRY

Tables at a glance
Table 1
Figures at a glance
Figure 1
Figure 2
Figure 3
Figure 4
Figure 5
Figure 6
Figure 7
Figure 8
Figure 9
Figure 1: Pear-shaped abdomen in a cow with ascites. Photo showing a pear-shaped abdomen in a Brown-Swiss cow with ascites due to compression of the caudal vena cava by two liver abscesses
Figure 2: Ultrasonogram of the reticular region. Ultrasonogram of the reticular region of a cow with ascites due to compression of the caudal vena cava by two liver abscesses, imaged from the sternal part of the ventral abdomen. The reticulum is displaced dorsally by anechoic ascites fluid. 1 Ventral abdominal wall, 2 Musculophrenic vein, 3 Diaphragm, 4 Ascites fluid, 5 Reticulum, 6 Anterior dorsal blind sac of the rumen, Cr Cranial, Cd Caudal
Figure 3: Ultrasonogram of ascites. Ultrasonogram of ascites in a cow with compression of the caudal vena cava by two liver abscesses, imaged from the right flank. Loops of small intestines are displaced dorsally by anechoic ascites fluid. 1 Lateral abdominal wall, 2 Extraomental ascites fluid, 3 Greater omentum, 4 Intraomental ascites fluid, 5 Small intestines, Ds Dorsal, Vt Ventral
Figure 4: Ultrasonogram of the liver and gallbladder. Ultrasonogram of the liver and gallbladder of a cow with ascites due to compression of the caudal vena cava by two liver abscesses, imaged from the 10th intercostal space on the right side. The liver and the gallbladder are displaced from the abdominal wall by anechoic ascites fluid. The wall of the gallbladder appears thicker than normal because of oedema (congestion). 1 Lateral abdominal wall, 2 Ascites fluid, 3 Liver, 4 Gallbladder, Ds Dorsal, Vt Ventral
Figure 5: Ultrasonogram of the caudal vena cava. Ultrasonogram of the caudal vena cava in a cow with compression of the caudal vena cava by two liver abscesses, imaged from the 11th intercostal space on the right side. The caudal vena cava, which normally is triangular in cross-section, is round because of congestion and dilation. 1 Lateral abdominal wall, 2 Liver, 3 Hepatic vein, 4 Caudal vena cava, 5 Right hepatic vein, Ds Dorsal, Vt Ventral
Figure 6: Yellow ascites fluid escapes from the peritoneal cavity. A large volume of yellow ascites fluid escapes from the peritoneal cavity after incision of the abdominal wall during postmortem examination of a Brown-Swiss cow with compression of the caudal vena cava by two liver abscesses
Figure 7: Liver with two abscesses. The diaphragmatic fascia of the liver of a Brown-Swiss cow with two abscesses (arrows) in the upper margin of the liver and immediately adjacent to the caudal vena cava. The liver is whitish-grey and enlarged because of congestion of the caudal vena cava
Figure 8: Pus oozes from an incised liver abscess. Yellow viscous pus (arrow) oozes from an incised liver abscess that was compressing the caudal vena cava in a Brown-Swiss cow
Figure 9: Opened caudal vena. The caudal vena cava (arrow) of a Brown-Swiss cow with compression of the vein by two liver abscesses. The incised and opened caudal vena cava has no macroscopic abnormalities, such as a thrombus
Variable
Cow
Normal range
Haematocrit (%)
38
33 – 36
γ-GT (U/l)
56
15 – 25
Urea (mmol/l)
7.7
3.5 – 6.5

Calcium (mmol/l)

2.1
2.3 – 2.6
Venous blood pH
7.36
7.40 – 7.50
Bicarbonate (mmol/l)
21.1
20 – 30
Base excess (mmol/l)
-3.1
-2 to +2
Table 1: Selected haematological and biochemical results and venous blood gas analysis in a cow with ascites secondary to compression of the caudal vena cava by liver abscesses

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