- Case report
- Open Access
Hepatic emphysema associated with ultrasound-guided liver biopsy in a dog
© Westgren et al.; licensee BioMed Central Ltd. 2014
- Received: 11 February 2014
- Accepted: 16 April 2014
- Published: 23 April 2014
An eleven-year-old Chinese Crested Powder Puff dog presented with polydipsia/polyuria, inappetence, diarrhea and vomiting underwent an ultrasound-guided percutaneous liver biopsy. Two days post-biopsy the clinical condition of the dog acutely deteriorated with fever, dyspnea, ataxia and subcutaneous emphysema. Radiographs and ultrasound showed focal severe hepatic emphysema in the region of the previous liver biopsy. Post-mortem examination revealed chronic hepatitis with dissecting fibrosis, acute hepatitis with hemorrhage and in the hindlimb musculature extensive hemorrhage and necrosis. Pure cultures of the gas producing bacteria Clostridium perfringens were isolated in samples from the hind limb musculature. We propose that the hepatic emphysema in the region of the biopsy site was a result of a clostridial infection.
- Clostridium perfringens
Liver biopsy, including both ultrasound-guided and blinded techniques, is considered a safe procedure with reported major complication rates between 0.01-5.9% of the cases in humans[1, 2] and low complication rates in dogs[3, 4]. In humans hemorrhage is the most commonly encountered major complication (0.2-1.7% of patients) and biliary peritonitis, hemobilia, hypotension, arteriovenousfistula, pulmonary embolism and ileus occur in less than 1% of the cases[1, 2]. Transient bacteriemia associated with liver biopsy has been shown with blood and liver tissue culture to have an incidence of 2-13%, but clinically evident infectious complications are considered extremely rare[1, 5]. The majority of the patients with liver biopsy associated bacteriemia have pathological changes consistent with hepatocellular or hepatobiliary disease[1, 5]. Furthermore defects in the patients defence mechanisms occur due to liver disease including deficiencies of serum complement, inhibition of chemotaxis, colonization of the small bowel by enteric organisms and bypass of bacterial clearance mechanisms via intrahepatic shunts[6, 7]. We present a case of hepatic emphysema associated with ultrasound-guided liver biopsy and possible clostridial bacteriemia.
Signalment, history and clinical findings
An 11-year-old male Chinese Crested Powder Puff was presented with progressive polyuria, polydipsia and inappetence. The general physical examination was normal except for a moderate systolic heart murmur. Biochemical tests revealed elevations of alanine aminotransferase (282 IU/l) [ref 0-78 IU/l], alkaline phosphatase (1812 IU/l) [ref 0-132 IU/l] and bile acids (14.7 μmol/l) [ref 0-12 μmol/l].
Imaging, diagnosis and outcome
Ultrasound-guided percutaneous liver biopsy was scheduled for the following week. Diarrhea and one episode of vomiting were observed on the day of the planned biopsy procedure but immediately prior to the biopsy procedure the clinical condition of the dog was considered stable and the dog had normal temperature, thus the biopsy was performed as planned.
A standard anesthetic protocol including propofol induction and isoflurane maintenance was used. Two free-hand ultrasound-guided percutaneous liver biopsies (18 gauge needle, BARD biopsy needle and BARD magnum biopsy instrument, Crawley, UK) using a longitudinal plane and targeting two of the focal heterogenous areas of the liver via a left cranial abdominal window were taken. The biopsy needle position was maintained to the left and dorsal to the gallbladder and the gallbladder avoided during penetration of the liver and firing of the biopsy device. No complications were detected during the procedure or when the biopsy region was scanned immediately after the procedure. The dog was discharged the following day since it was reported to be bright and alert with normal temperature and only one occasion of diarrhea and vomit had occurred post-biopsy.
The dog was returned to the clinic two days later when the owner reported that the diarrhea and vomiting had increased in frequency and the general condition of the dog had acutely deteriorated. Clinical examination revealed fever, dyspnea, ataxia and subcutaneous emphysema. Laboratory tests showed neutrophilia with moderate left-shift, hundredfold increased value of C-reactive protein and a mixed metabolic acidosis and respiratory alkalosis (HCO3− 15.6 mmol/l [ref 22.2-27.2 mmol/l] and PCO2 19.1 kPa [31.8-54 kPa]).
Post-mortem examination revealed acute hepatitis with hemorrhage, chronic hepatitis with dissecting fibrosis, and hepatic nodular hyperplasia. An extensive acute necrotizing hemorrhagic myositis was seen in the hind limb musculature. The intestinal mucosa was autolytic but a mild to moderate infiltration of lymphocytes and plasma cells was noted. Focal chronic pancreatitis and nodular hyperplasia, chronic glomerulonephritis with focal areas of emphysema in the renal cortex, and a chronic hemorrhagic cystitis was diagnosed, as was myxomatous valvular degeneration of the mitral valves and cardiac hemorrhage. Swabs were taken from the hind limb musculature for bacteriology and Clostridium perfringens was isolated in pure culture. Samples for bacteriology were not taken from the liver.
The culture of C. perfringens from the hindlimb muscles combined with areas of acute hepatic hemorrhages and gas production in the liver and kidneys strongly suggested bacteriemia and focal clostridial infection of the liver biopsy site in this dog. C. perfringens is a toxin producing commensal opportunistic anaerobic bacteria reported to be found in the bowel and heptobiliary tree of some individuals[8, 9]. The bacteria can spread hematogenously, biliary or by wound penetration. It is possible in this case that the liver biopsy caused propagation of C. perfringens bacteria from the bile ducts due to communication between infected focus and blood vessels, resulting in systemic bacteriemia. More than 50% of biliary tract infections is due to C. perfringens in humans and it has been shown to be one of the most common isolates in dogs and cats with hepatobiliary disease. The diarrhea of the dog is a potential reason for the spread of C. perfringens to the liver by reflux from the intestine into the bile ducts. Bile culture was not carried out to confirm or exclude the presence of bacteria at the time of the biopsy procedure or post-mortem examination. Introduction of bacteria into the liver parenchyma by the biopsy needle is another possibility, although surgical preparation of the skin and the use of sterile biopsy needle makes this unlikely. Alternatively a hematogenous route of systemic spread of bacteria from the intestines is possible, with focal hepatic emphysema developing as a consequence of less resistance of the liver parenchyma following the mechanical damage by the biopsy needle in combination with chronic liver disease. Several risk factors for anaerobic blood stream infection preexisted in this dog including intestinal disease, chronic liver disease and heart disease[10, 12]. Previous antimicrobial treatment at the referral clinic could potentially have disrupted the microenvironment of the gastrointestinal tract and enabled proliferation of C. perfringens. A penetrating wound of the hindlimb coinciding with the liver biopsy procedure and the gastrointestinal symptoms is another possible explanation for the bacterial infection that cannot be completely excluded, although no wound was found at post-mortem examination.
This report shows a case of focal hepatic emphysema associated with percutaneous ultrasound-guided liver biopsy, suspected to be a result of a clostridial infection. Careful selection and preparation of patients, including identification of potential infection of the biliary or gastrointestinal tract, prior to liver biopsy is recommended.
- Claudi C, Henschel M, Vogel J, Schepke M, Biecker E: Fulminant sepsis after liver biopsy: a long forgotten complication?. World J Clin Cases. 2013, 1: 41-43. 10.12998/wjcc.v1.i1.41.PubMed CentralView ArticlePubMedGoogle Scholar
- Larson AM, Chan GC, Wartelle CF, McVicar JP, Carithers RL, Hamill GM, Kowdley KV: Infection complicating percutaneous liver biopsy in liver transplant recipients. Hepatology. 1997, 26: 1406-1409. 10.1002/hep.510260605.View ArticlePubMedGoogle Scholar
- Hager DA, Nyland TG, Fisher P: Ultrasound-guided biopsy of the canine liver, kidney, and prostate. Vet Radiol. 1985, 26: 82-88. 10.1111/j.1740-8261.1985.tb01388.x.View ArticleGoogle Scholar
- Barr F: Percutaneous biopsy of abdominal organs under ultrasound guidance. J Small Anim Pract. 1995, 36: 105-113. 10.1111/j.1748-5827.1995.tb02843.x.View ArticlePubMedGoogle Scholar
- Le Frock JL, Ellis CA, Turchik JB, Zawacki JK, Weinstein L: Transient bacteremia associated with percutaneous liver biopsy. J Infect Dis. 1975, 131 (Suppl): S104-107.View ArticlePubMedGoogle Scholar
- McCloskey RV, Gold M, Weser E: Bacteremia after liver biopsy. Arch Intern Med. 1973, 132: 213-215. 10.1001/archinte.1973.03650080057011.View ArticlePubMedGoogle Scholar
- Cheruvattath R, Balan V: Infections in patients with end-stage liver disease. J Clin Gastroenterol. 2007, 41: 403-411. 10.1097/01.mcg.0000248018.08515.f9.View ArticlePubMedGoogle Scholar
- McIlwaine K, Leach MT: Clostridium perfringens septicaemia. Br J Haematol. 2013, 163: 549-10.1111/bjh.12551.View ArticlePubMedGoogle Scholar
- Goldstein MR, Kruth SA, Bersenas AM, Holowaychuk MK, Weese JS: Detection and characterization of Clostridium perfringens in the feces of healthy and diarrheic dogs. Can J Vet Res. 2012, 76: 161-165.PubMed CentralPubMedGoogle Scholar
- Huang WC, Lee WS, Chang T, Ou TY, Lam C: Emphysematous cholecystitis complicating liver abscess due to Clostridium baratii infection. J Microbiol Immunol Infect. 2012, 45: 390-392. 10.1016/j.jmii.2011.12.007.View ArticlePubMedGoogle Scholar
- Wagner KA, Hartmann FA, Trepanier LA: Bacterial culture results from liver, gallbladder, or bile in 248 dogs and cats evaluated for hepatobiliary disease: 1998-2003. J Vet Intern Med. 2007, 21: 417-424.PubMedGoogle Scholar
- Ngo JT, Parkins MD, Gregson DB, Pitout JD, Ross T, Church DL, Laupland KB: Population-based assessment of the incidence, risk factors, and outcomes of anaerobic bloodstream infections. Infection. 2013, 41: 41-48. 10.1007/s15010-012-0389-4.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.