SURGICAL INFECTIONS Volume 14, Number 4, 2013 ª Mary Ann Liebert, Inc. DOI: 10.1089/sur.2012.142
Letters to Surgical Infections
Perinephric Abscess Due to Achromobacter xylosoxidans following De-Roofing of Renal Cyst Vivek Vinod,1 Anil Kumar,1 Kalavampara V. Sanjeevan,2 Kavitha R. Dinesh,1 and Shamsul Karim1
To the Editor:
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51-year-old male, who had undergone laparoscopic deroofing of a simple renal cyst on the left side two years ago, presented with left flank pain of one month’s duration near the port site, along with low-grade fever. There was no abdominal distension or mass, nor alteration in bladder or bowel habits. He was not a diabetic nor had he any other important medical history. Physical examination revealed a temperature of 100.4F, soft abdomen with severe tenderness over the left iliac fossa, and unremarkable left flank and costovertebral angle. The white blood cell count was 19,000/mcL, and the serum creatinine concentration was 1.52 mg/dL. A magnetic resonance imaging scan of the abdomen revealed a collection with enhancing septations in the left posterior pararenal space, extending into the psoas and quadratus lumborum muscles and adhering to the posterolateral abdominal wall. There was left perirenal stranding (Fig. 1) and a small left renal upper polar cortical cyst (Fig. 2). Blood and urine culture studies yielded no growth. Empiric antibiotic therapy was of no benefit and the patient returned with a pointing abscess about to rupture. The collection was incised and drained after ruling out any urine leak from the left upper urinary tract by retrograde urography, and a closed suction drain was left in the abscess cavity. The pus sample sent for culture yielded growth of nonfermenting gram-negative bacilli, identified by VITEK 2 compact system (bioMe´rieux, Inc., St Louis, MO) as Achromobacter xylosoxidans with a 99% probability and an ‘‘excellent identification’’ confidence level. The isolate was susceptible to piperacillin, levofloxacin, co-trimoxazole, ceftazidime, cefoperazone-sulbactam, and meropenem, but resistant to aminoglycosides and tetracycline using Clinical and Laboratory Standards Institute (CLSI) break points for nonEnterobacteriaceae. The drain was removed on the fifth post-operative day and the patient was discharged on oral levofloxacin and cotrimoxazole. Three days after discharge, the patient returned in sepsis with similar complaints and pus draining from the incision. On retaking the history, it was determined that the patient had stopped taking the antibiotics after discharge. On examination, his temperature was 101.6F and he had tenderness of the left flank. Abdominal ultrasonogram showed
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minimal residual collection at the abscess site. A second incision and drainage was performed immediately under cover of intravenous cefoperazone-sulbactam. A small amount of purulent material was drained and the abscess wall was debrided. The benign-looking small cortical cyst towards the upper pole was left undisturbed on both occasions. After 1 wk of intravenous antibiotic and supportive therapy, the patient was discharged in good health on oral co-trimoxazole and levofloxacin for 2 wks. On clinic follow-ups at 1 mo and 3 mos, there was no evidence of any continuing infection or any local symptom or abnormal findings on imaging studies other than the unchanged cortical cyst. Achromobacter xylosoxidans is a non-fermenting gramnegative, motile oxidase-positive bacillus belonging to the Alcaligenaceae family [1]. It is characterized by the ability to utilize xylose and glucose oxidatively. Identification using traditional phenotypic test often is unreliable and A. xylosoxidans can be mistaken for non-aeruginosa strains of Pseudomonas or for strains of Burkholderia cepacia complex. Achromobacter xylosoxidans is an opportunistic pathogen capable of causing nosocomial and community-acquired infections, with the source being either endogenous or from a contaminated aquatic hospital environment [2]. It frequently has been iso-
FIG. 1. Magnetic resonance image showing pararenal collection in relation to the lower aspect of left kidney.
Department of Microbiology, 2Department of Urology, Amrita Institute of Medical Sciences, Ernakulam, Kerala, India.
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LETTERS TO SURGICAL INFECTIONS
423 may rupture subsequently. The choice of therapy is to drain all but the smallest collection and correct any treatable underlying cause. For a large abscess with septae and loculation, a drain should be left in situ with repositioning as needed for complete evacuation. In culture-positive abscess cases, only 67% usually grow the same organism in urine or blood [10]. In our case, there was no simultaneous isolation of the pathogen from another samples. Apart from making the first report of a perinephric abscess due to A. xylosoxidans, our article also highlights the possibility of developing such an infection in the absence of any residual foreign body in an otherwise immunocompetent individual. References
FIG. 2. Magnetic resonance image showing pararenal collection extending to the left psuas, quadratus and adjacent oedematous abdominal wall.
lated from blood, cerebrospinal fluid, pus, and urine. Central venous catheters, mechanical ventilators, tubing of apparatus used for dispensing disinfectants (didecyl dimethyl ammonium chloride), and contaminated dialysis fluids have been implicated as sources of infection in many hospitalized patients [3]. It is also known to colonize and infect the respiratory tract in cases of cystic fibrosis [4]. Achromobacter spp. has been reported to cause abscesses in the liver [2], pancreas [5], urinary bladder [6], skeletal muscle [6], and aortic root [12]. A complicated intra-abdominal abscess caused by A. xylosoxidans following surgery in an acute cholecystitis patient was reported from Taiwan in 2009 [13]. The mortality rate ranges from 15% to 48% and is found to be high in patients with risk factors such as neutropenia, advanced age, nosocomial infection, and polymicrobial infection [3]. To the best of our knowledge, A. xylosoxidans infection as a cause of perinephric abscess has not been reported perviously. Moreover, this abscess occurred in the absence of any foreign body in an otherwise immunocompetent individual. There is one report of A. xylosoxidans causing pelvic and paravesical abscess about 25 years after hernia repair with mesh [6]. Achromobacter xylosoxidans shows high-level resistance to aminoglycosides, cephalosporins, and quinolone antibiotics. Our patient presented with the infection 2 y after de-roofing of a renal cyst. He is likely to have acquired a nosocomial strain of the pathogen during the operation. Perinephric abscess may remain silent and may be detected only during incidental imaging [9]. They usually occur because of parenchymal disruption as a consequence of raised intra-pelvic pressure caused by an obstructing stone. Hematologic dissemination may result in the formation of abscess in 30% of cases, which
1. Winn W Jr, Allen S, Janda W, et al. Koneman’s Color Atlas and Textbook of Diagnostic Microbiology, 6th ed. Philadelphia, PA:Lippincott Williams and Wilkins, 2006:340–343. 2. Asano K, Tada S, Matsumoto T, et al. A novel bacterium Achromobacter xylosoxidans as a cause of liver abscess: Three case reports. J Hepatol 2005;43:362–365. 3. Gomez-Cerezo J, Suarez I, Rios JJ, et al. Achromobacter xylosoxidans bacteremia: A 10-year analysis of 54 cases. Eur J Clin Microbiol Infect Dis 2003;22:360–363. 4. Pereira RH, Carvalho-Assef AP, Albano RM, et al. Achromobacter xylosoxidans: Characterization of strains in Brazilian cystic fibrosis patients. J Clin Microbiol 2011;49:3649–3651. 5. Appelbaum PC, Campbell DB. Pancreatic abscess associated with Achromobacter group Vd biovar 1. J Clin Microbiol 1980;2:282–283. 6. Frail G, Gallego JI, Martinez-Molina E, Meseur MA. Psoas and paravesical abscess formation due to Achromobacter xylosoxidans: A case report. Eferm Infecc Microbiol Clin 2010;28: 325–326. 7. van Hal S, Stark D, Marriott D, Harkness J. Achromobacter xylosoxidans subsp xylosoxidans prosthetic aortic valve infective endocarditis and aortic root abscesses. J Med Microbiol. 2008;57:525–527. 8. Shu T, Green JM, Orihuela E. Renal and perirenal abscess in patients with otherwise anatomically normal urinary tracts. J Urol 2004;172:148–150. 9. Gardiner RA, Gwynne RA, Roberts SA. Perinephric abscess. BJU Int 2011;07:20–23.
Address correspondence to: Mr. Vivek Vinod Department of Microbiology Amrita Institute of Medical Sciences AIMS Ponekkara P.O. Edapally Ernakulam, Kerala India 682041 E-mail:
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