ISPUB.com / IJOS/32/1/57012
  • Author/Editor Login
  • Registration
  • Facebook
  • Google Plus

ISPUB.com

Internet
Scientific
Publications

  • Home
  • Journals
  • Latest Articles
  • Disclaimers
  • Article Submissions
  • Contact
  • Help
  • The Internet Journal of Orthopedic Surgery
  • Volume 32
  • Number 1

Case Study

Septic Arthritis Of The Finger Due To Corynebacterium Argentoratense

J Wong, Y Leung

Citation

J Wong, Y Leung. Septic Arthritis Of The Finger Due To Corynebacterium Argentoratense. The Internet Journal of Orthopedic Surgery. 2024 Volume 32 Number 1.

DOI: 10.5580/IJOS.57012

Abstract

We report a case of native finger joint septic arthritis due to Corynebacterium argentoratense in a healthy immunocompetent 50-year-old woman after a penetrating injury. The patient was successfully treated with open debridement and synovectomy followed by 6-week course of oral Doxycycline. Despite being a ubiquitous human commensal and often considered contaminant when isolated in culture, our report further confirms the pathogenic role of Corynebacterium species in certain clinical circumstances. To the authors’ knowledge, this is also the first reported case of septic arthritis due to C. argentoratense.

 

Introduction

Corynebacterium is a genus of club-shaped Gram-positive bacilli and a common commensal in human skin and mucosal membranes. They were historically considered contaminants when isolated in culture, but have been increasingly recognized as emerging pathogens causing device-related infections and opportunistic infections in immunocompromised patients, including respiratory tract infections, endocarditis, and bone and joint infections [1-2].

Corynebacterium argentoratense was first identified in 1995 from the throat specimens of patients with tonsillitis in France [3], and since it has only been sporadically isolated from specimens of the respiratory tract, blood culture, conjunctiva and mucosal biofilm in adenoid tissues [3-4]. Herein, we report the first case of C. argentoratense septic arthritis of a native finger joint following a penetrating injury in a healthy immunocompetent patient.

Case presentation

A 50-year-old woman was referred to our clinic for a 1-month history of persistent right middle finger swelling after a penetrating injury by a sea urchin sting. Her past medical history included hyperlipidemia, and right ring finger enchondroma that was treated operatively with curettage and bone grafting more than 10 years ago. Prior to presenting to our unit, she was treated by a general practitioner and was given a course of oral Augmentin (amoxycillin and clavulanic acid).

On physical examination, there was swelling and erythema around the right middle finger’s proximal interphalangeal joint (PIPJ). The PIPJ was tender on palpation, but there was no obvious joint effusion nor collection. The active range of motion was full. Plain x-ray of the finger revealed no bony erosion nor presence of a radio-opaque foreign body (Figure 1). Blood tests including serum white blood cell count, C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), urate, as well as a panel of autoimmune markers (rheumatoid factor, and antinuclear antibodies) were all unremarkable. It was initially treated as cellulitis and the patient was given a course of oral Levofloxacin.

The patient was reviewed in our clinic after completing the course of antibiotic, at two months after the initial injury. There was improvement of swelling and tenderness around the affected joint. There was no joint effusion and the active range of motion was full. Thus, we opted for observation at that juncture. However, over the subsequent six months, she had persistent mild residual swelling and tenderness at the affected joint. Magnetic resonance imaging (MRI) of her right middle finger demonstrated synovial thickening with associated contrast enhancement suggestive of synovitis at the PIPJ (Figure 2). There was no rim enhancing collection, foreign body, nor evidence of bony erosion. The patient elected to proceed with operative treatment. Open arthrotomy was performed between the central slip and the radial lateral band. Synovitis and mild degenerative changes of the PIPJ were observed intraoperatively. Synovectomy was performed. Histological study of the synovial tissue revealed chronic synovitis with foreign body granulomas. Culture of the synovial tissue was positive for C. argentoratense. The patient was given a 6-week course of oral Doxycycline based on the susceptibility testing.

At 3-months follow-up, the surgical wound had healed well with no sign of infection. The right middle finger PIPJ swelling had completely resolved. The active range of motion was full and painless. Plain x-ray revealed no bony erosion.

Figure 1

Figure 2

Discussion

Corynebacterium is a non-sporulating, non-acid fast, non-branching, club-shaped Gram-positive bacilli that are aerobic and facultative anaerobic. With the exception of C. diphtheriae, the rest of the species are common commensal in human skin and mucosal membranes. Over the recent decades, they have been increasingly recognized as emerging pathogens causing device-related infections and opportunistic infections in immunocompromised patients including respiratory tract infections, endocarditis, and bone and joint infections [1-2]. However, septic arthritis at a native joint caused by Corynebacterium species are rare. Sporadic cases have been reported in the medical literature, and the species isolated included C. diphtheriae, C. pyogenes, C. xerosis, C. kutscheri, C. amycolatum, C. pseudodiphtheriticum, and C. striatum (Table 1).

Table 1
Cases of native joint septic arthritis caused by Corynebacterium species

To our knowledge, this is the only reported case of septic arthritis due to C. argentoratense. C. argentoratense was first identified in 1995 from the throat specimens of patients with tonsillitis in France [3]. It is a nonlipophilic, facultative anaerobic, nitrate reductase-negative, urease-negative, and oxidase-negative corynebacterium capable of utilizing glucose but not maltose nor sucrose [4]. Antimicrobial resistance to β-lactams, erythromycin and clindamycin has been reported [4]. Similar pattern of antimicrobial susceptibility was found in this case. The isolated C. argentoratense from the synovial tissue demonstrated resistance to penicillin G, moxifloxacin and clindamycin, whereas it was susceptible to doxycycline and vancomycin. Trial of oral Doxycycline was commenced and later continued for a total of 6 weeks because of the good clinical response it gave.

In the present case, C. argentoratense was most likely introduced into the finger joint from the penetrating injury. Having the organism isolated from the intraoperatively and aseptically collected synovial tissue sample confirmed that it was the primary pathogen and a genuine infection. In fact, half of the reported cases of Corynebacterium-associated native joint septic arthritis were preceded by trauma or instrumentation to the affected joint such as arthrocentesis and intraarticular injection [Table 1]. In essence, although Corynebacterium is a common human commensal, when it is introduced into a joint, it has the potential to cause septic arthritis even in an otherwise healthy immunocompetent person. Given that Corynebacterium infection often presents as a subacute or even indolent infection, it can potentially lead to a delay in diagnosis and treatment. A high degree of suspicion should be warranted when there is a history of trauma or instrumentation to the affected joint. Early detection and appropriate treatment is important to improve clinical outcomes.

Conclusion

We report for the first time a case of C. argentoratense-associated septic arthritis of a native finger joint after a penetrating injury. The infection was successfully treated with open debridement and synovectomy, followed by a 6-week course of oral Doxycycline. Our report further confirms the pathogenic role of Corynebacterium species in certain clinical circumstances. Our report also demonstrates that oral antibiotic treatment can be effective, allowing ambulatory care of the patient, while sparing the potential complications associated with prolonged hospitalization, intravenous access and vancomycin therapy.

References

1. Bernard K. (2012). The genus corynebacterium and other medically relevant coryneform-like bacteria. Journal of clinical microbiology, 50(10), 3152–3158. https://doi.org/10.1128/JCM.00796-12
2. Roux, V., Drancourt, M., Stein, A., Riegel, P., Raoult, D., & La Scola, B. (2004). Corynebacterium species isolated from bone and joint infections identified by 16S rRNA gene sequence analysis. Journal of clinical microbiology, 42(5), 2231–2233. https://doi.org/10.1128/JCM.42.5.2231-2233.2004
3. Riegel, P., Ruimy, R., De Briel, D., Prevost, G., Jehl, F., Bimet, F., Christen, R., & Monteil, H. (1995). Corynebacterium argentoratense sp. nov., from the human throat. International journal of systematic bacteriology, 45(3), 533–537. https://doi.org/10.1099/00207713-45-3-533
4. Fernández-Natal, I., Sáez-Nieto, J. A., Rodríguez-Lázaro, D., Valdezate-Ramos, S., Parras-Padilla, T., Medina, M. J., Rodríguez-Pollán, R. H., Blom, J., Tauch, A., & Soriano, F. (2016). Phenotypic, molecular characterization, antimicrobial susceptibility and draft genome sequence of Corynebacterium argentoratense strains isolated from clinical samples. New microbes and new infections, 10, 116–121. https://doi.org/10.1016/j.nmni.2016.01.007
5. Norenberg, D. D., Bigley, D. V., Virata, R. L., & Liang, G. C. (1978). Corynebacterium pyogenes septic arthritis with plasma cell synovial infiltrate and monoclonal gammopathy. Archives of internal medicine, 138(5), 810–811.
6. Guran, P., Mollaret, H. H., Chatelain, R., Gropman, M., Prigent, F., & Béal, G. (1979). Arthrite purulente à bacille diphtérique atoxinogene [Septic arthritis due to a nontoxigenic diphtheria bacillus]. Archives francaises de pediatrie, 36(9), 926–929.
7. Appelbaum, P. C., & Dossett, J. H. (1982). Arthritis caused by unidentified gram-positive rods in a child with acute lymphocytic leukemia. Journal of clinical microbiology, 15(3), 525–527. https://doi.org/10.1128/jcm.15.3.525-527.1982
8. Valenstein, P., Klein, A., Ballow, C., & Greene, W. (1988). Corynebacterium xerosis septic arthritis. American journal of clinical pathology, 89(4), 569–571. https://doi.org/10.1093/ajcp/89.4.569
9. Messina, O. D., Maldonado-Cocco, J. A., Pescio, A., Farinati, A., & García-Morteo, O. (1989). Corynebacterium kutscheri septic arthritis. Arthritis and rheumatism, 32(8), 1053. https://doi.org/10.1002/anr.1780320819
10. Booth, L. V., Richards, R. H., & Chandran, D. R. (1991). Septic arthritis caused by Corynebacterium xerosis following vascular surgery. Reviews of infectious diseases, 13(4), 548–549. https://doi.org/10.1093/clinids/13.4.548
11. Afghani, B., & Stutman, H. R. (1993). Bacterial arthritis caused by Corynebacterium diphtheriae. The Pediatric infectious disease journal, 12(10), 881–882. https://doi.org/10.1097/00006454-199310000-00017
12. Barakett, V., Morel, G., Lesage, D., & Petit, J. C. (1993). Septic arthritis due to a nontoxigenic strain of Corynebacterium diphtheriae subspecies mitis. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 17(3), 520–521. https://doi.org/10.1093/clinids/17.3.520
13. Damade, R., Pouchot, J., Delacroix, I., Boussougant, Y., & Vinceneux, P. (1993). Septic arthritis due to Corynebacterium diphtheriae. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 16(3), 446–447. https://doi.org/10.1093/clind/16.3.446
14. Cone, L. A., Curry, N., Wuestoff, M. A., O'Connell, S. J., & Feller, J. F. (1998). Septic synovitis and arthritis due to Corynebacterium striatum following an accidental scalpel injury. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 27(6), 1532–1533. https://doi.org/10.1086/517737
15. Clarke, R., Qamruddin, A., Taylor, M., & Panigrahi, H. (1999). Septic arthritis caused by Corynebacterium amycolatum following vascular graft sepsis. The Journal of infection, 38(2), 126–127. https://doi.org/10.1016/s0163-4453(99)90082-8
16. Faraj, S., French, J. G., & McAuslan, A. (2003). Septic arthritis due to a toxigenic strain of Corynebacterium diphtheriae gravis. The New Zealand medical journal, 116(1172), U404.
17. Scholle D. (2007). A spontaneous joint infection with Corynebacterium striatum. Journal of clinical microbiology, 45(2), 656–658. https://doi.org/10.1128/JCM.00827-06
18. Boltin, D., Katzir, M., Bugoslavsky, V., Yalashvili, I., Brosh-Nissimov, T., Fried, M., & Elkayam, O. (2009). Corynebacterium striatum--a classic pathogen eluding diagnosis. European journal of internal medicine, 20(3), e49–e52. https://doi.org/10.1016/j.ejim.2008.08.009
19. Erturan, G., Holme, H., & Iyer, S. (2012). Corynebacterium pseudodiphtheriticum septic arthritis secondary to intra-articular injection--a case report and literature review. Journal of medical microbiology, 61(Pt 6), 860–863. https://doi.org/10.1099/jmm.0.037937-0
20. Feced Olmos, C. M., Alegre Sancho, J. J., Ivorra Cortés, J., & Román Ivorra, J. A. (2013). Septic arthritis of the shoulder due to Corynebacterium striatum. Reumatologia clinica, 9(6), 383. https://doi.org/10.1016/j.reuma.2013.02.006
21. Westblade, L. F., Shams, F., Duong, S., Tariq, O., Bulbin, A., Klirsfeld, D., Zhen, W., Sakaria, S., Ford, B. A., Burnham, C. A., & Ginocchio, C. C. (2014). Septic arthritis of a native knee joint due to Corynebacterium striatum. Journal of clinical microbiology, 52(5), 1786–1788. https://doi.org/10.1128/JCM.02641-13
22. Roy, M., & Ahmad, S. (2016). Rare case of Corynebacterium striatum septic arthritis. BMJ case reports, 2016, bcr2016216914. https://doi.org/10.1136/bcr-2016-216914
23. Molina Collada, J., Rico Nieto, A., Díaz de Bustamante Ussia, M., & Balsa Criado, A. (2018). Septic arthritis in a native knee due to Corynebacterium striatum. Artritis séptica de rodilla nativa por Corynebacterium striatum. Reumatologia clinica, 14(5), 301–302. https://doi.org/10.1016/j.reuma.2017.01.013
24. Hollnagel, K., Willen, J., Ellis, M., Soleimanifard, Y., Booth, R., & Nandi, S. (2020). Chronic Corynebacterium striatum Septic Arthritis in a Patient Referred for Total Knee Arthroplasty. Case reports in orthopedics, 2020, 1392182. https://doi.org/10.1155/2020/1392182
25. Umemoto, D., Hara, S., & Nishioka, H. (2023). Infective endocarditis and septic arthritis caused by Corynebacteriumstriatum. Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, S1341-321X(23)00313-6. Advance online publication. https://doi.org/10.1016/j.jiac.2023.12.009

Author Information

Justin Hoi Lui Wong
Department of Orthopaedics and Traumatology, Tseung Kwan O Hospital
Hong Kong SAR, China

Yuen-Fai Leung
Department of Orthopaedics and Traumatology, Tseung Kwan O Hospital
Hong Kong SAR, China

Download PDF

Your free access to ISPUB is funded by the following advertisements:

 

BACK TO TOP
  • Facebook
  • Google Plus

© 2013 Internet Scientific Publications, LLC. All rights reserved.    UBM Medica Network Privacy Policy