Abstract
At laboratory examination his white blood cell count was 19 000 cells µl–1, he had 10.2 g haemoglobin dl–1, 137 mg glucose dl–1, 5.9 g total protein dl–1 and 0.9 g albumin dl–1. Other biochemical parameters were within normal limits. No findings of osteomyelitis were determined in pelvic and thigh images. After blood cultures (BACTEC 9200; Becton Dickinson) and aerobic and anaerobic cultures had been taken from the wound, the patient was prepared for surgery and the entire pelvic anterolateral trochanteric area was debrided.
Upon microscopic examination of the debridement material, Gram-positive cocci chains and abundant polymorphonuclear leukocytes were observed. The material was cultured in aerobic and anaerobic jars using the BACTEC system (Becton Dickinson). Treatment with 200 mg ciprofloxacin and 600 mg clindamycin was initiated, twice a day and four times a day, respectively.
Enterobacter cloacae and meticillin-resistant coagulase-negative staphylococci growth was found in aerobic cultures taken before debridement, and R. productus growth was found in anaerobic culture of the debridement material. Identification was performed using a Sceptor panel (Becton Dickinson). There was no growth in the aerobic culture. Treatment was changed to 500 mg imipenem four times a day+1000 mg amikacin once a day+400 mg teicoplanin once a day. The defective area in the patient, monitored on a daily basis in the postoperative period with wound care and using antibiotherapy, was repaired with a split thickness skin graft taken from the contralateral thigh. The patient was discharged without complication on day 65 after admission.
At laboratory examination his white blood cell count was 19 000 cells µl–1, he had 10.2 g haemoglobin dl–1, 137 mg glucose dl–1, 5.9 g total protein dl–1 and 0.9 g albumin dl–1. Other biochemical parameters were within normal limits. No findings of osteomyelitis were determined in pelvic and thigh images. After blood cultures (BACTEC 9200; Becton Dickinson) and aerobic and anaerobic cultures had been taken from the wound, the patient was prepared for surgery and the entire pelvic anterolateral trochanteric area was debrided.
Upon microscopic examination of the debridement material, Gram-positive cocci chains and abundant polymorphonuclear leukocytes were observed. The material was cultured in aerobic and anaerobic jars using the BACTEC system (Becton Dickinson). Treatment with 200 mg ciprofloxacin and 600 mg clindamycin was initiated, twice a day and four times a day, respectively.
Enterobacter cloacae and meticillin-resistant coagulase-negative staphylococci growth was found in aerobic cultures taken before debridement, and R. productus growth was found in anaerobic culture of the debridement material. Identification was performed using a Sceptor panel (Becton Dickinson). There was no growth in the aerobic culture. Treatment was changed to 500 mg imipenem four times a day+1000 mg amikacin once a day+400 mg teicoplanin once a day. The defective area in the patient, monitored on a daily basis in the postoperative period with wound care and using antibiotherapy, was repaired with a split thickness skin graft taken from the contralateral thigh. The patient was discharged without complication on day 65 after admission.
A 63-year-old male patient had inflammation and swelling in the left leg and foot for the previous 10 days. He had a history of a minimal thermal injury from a stove 2 weeks before. This had worsened significantly over the preceding few days, inflammation had advanced and a vesicle with a yellowish appearance had also developed. The patient had a 20 year history of diabetes mellitus and a 10 year history of congestive heart failure. He was in the stock-breeding line of work. His general condition at physical examination was good. Vesicles containing purulent material were present in the oedematous left leg and foot. His temperature was 37 °C, he had 363 mg glucose dl–1, a white blood cell count of 22 500 cells µl–1 and 11.8 g haemoglobin dl–1. Other laboratory findings were within normal limits. Upon microscopic examination of material taken from the wound, Gram-positive coccus chains and clusters and abundant polymorphonuclear leukocytes were observed. Aerobic and anaerobic cultures were taken, after which 200 mg ciprofloxacin and 600 mg clindamycin was started, twice a day and four times a day, respectively. Once the appropriate conditions had been established, debridement was performed and the patient followed-up with wound care. Growth in the cultures taken was identified using an automated Sceptor panel (Becton Dickinson). Meticillin-resistant coagulase-negative staphylococci grew in aerobic culture and R. productus in anaerobic culture of the debridement material. The treatment was changed to 500 mg imipenem four times a day+1000 mg amikacin once a day+400 mg teicoplanin once a day. When the wound floor became suitable 3 weeks later, a repair was performed using a split thickness skin graft. The patient was discharged without complication 42 days after admission. Necrotizing fasciitis has been known for many years, but the term was first employed by Wilson in 1952. Wilson described necrotizing fasciitis as a soft tissue infection spreading along the fascias (Wilson, 1952). Necrotizing fasciitis is a rarely seen but severe infection characterized by rapid progression along the subcutaneous tissues. It has a high mortality rate, ranging between 6 and 76 % (Hasham et al., 2005). Immunosuppression, diabetes, chronic disease, malnutrition, intravenous drug use, alcohol abuse, peripheral vascular disease, renal failure, blunt or penetrating trauma, surgery, burns, muscle injuries and hypertension may be observed as predisposing factors (Hasham et al., 2005; Rieger et al., 2007). Patients' initial symptoms may be swelling, inflammation, skin colour changes and systemic findings, leading to a picture of severe infection (Hasham et al., 2005). Necrotizing fasciitis frequently occurs as a polymicrobial infection involving aerobic and anaerobic bacteria, though a single agent has been determined in 15 % of cases. Polymicrobial agents were determined in both cases presented in this report. Of these, R. productus may colonize the upper respiratory tract, gastrointestinal tract, vagina and skin in humans and animals (Sucu et al., 2006). Despite occurring in the intestinal flora, this bacterium seldom appears as an infective agent. The presence of type II diabetes in both our patients and the fact that both raised livestock may be regarded as predisposing factors.There are few reports in the literature of infections arising through this bacterium; it is rarely isolated in clinical specimens (Sucu et al., 2006; Nakatani et al., 1998; Botha et al., 1993; Sklavounos et al., 1986). Sucu et al. (2006) from our hospital reported that they had isolated R. productus in cases of liver abscess and infective endocarditis. Nakatani et al. (1998) isolated P. productus as an agent in epidural abscess, and Botha et al. (1993) and Sklavounos et al. (1986) in orofacial abscess cases. Bezirtzoglou & Romond (1991) showed that P. productus may colonize in the first day of life in ocular conjunctivitis in neonates delivered by Caesarean section.
In conclusion, although ruminococci do not often appear as infective agents, they may appear in the presence of predisposing factors. In such cases developing necrotizing fasciitis, deep tissue cultures should be taken promptly and rarely observed infective agents borne in mind. To the best of our knowledge, at the time of submission of this report, there were no cases in the literature in which R. productus was considered as an agent in necrotizing fasciitis.
References
Botha, S. J., Senekal, R., Steyn, P. L. & Coetzee, W. J. (1993). Anaerobic bacteria in orofacial abscesses. J Dent Assoc S Afr 48, 445–449.[Medline]
Ezaki, T., Li, N., Hashimoto, Y., Miura, H. & Yamamoto, H. (1994). 16S ribosomal DNA sequences of anaerobic cocci and proposal of Ruminococcus hansenii comb. nov. and Ruminococcus productus comb. nov. Int J Syst Bacteriol 44, 130–136.
Hasham, S., Matteucci, P., Stanley, P. R. & Hart, N. B. (2005). Necrotising fasciitis. BMJ 330, 830–833.
Nakatani, S., Hoshi, K., Yuasa, T., Sato, T. & Tauchi, T. (1998). A case report of epidural abscess due to anaerobic bacteria, producing a mass of gas. Rinsho Shinkeigaku 38, 224–227 (in Japanese).[Medline]
Rieger, U. M., Gugger, C. Y., Farhadi, J., Heider, I., Andresen, R., Pierer, G. & Scheufler, O. (2007). Prognostic factors in necrotizing fasciitis and myositis: analysis of 16 consecutive cases at a single institution in Switzerland. Ann Plast Surg 58, 523–530.[CrossRef][Medline]
Sklavounos, A., Legakis, N. J., Ioannidou, H. & Patrikiou, A. (1986). Anaerobic bacteria in dentoalveolar abscesses. Int J Oral Maxillofac Surg 15, 288–291.[Medline]
Sucu, N., Koksal, I., Yilmaz, G., Aydin, K., Caylan, R. & Aktoz-Boz, G. (2006). Liver abscess and infective endocarditis cases caused by Ruminococcus productus. Mikrobiyol Bul 40, 389–395.[Medline]
Wilson, B. (1952). Necrotising fasciitis. Am Surg 18, 416–431.[Medline]
Wong, C. H., Chang, H. C., Pasupathy, S., Khin, L. W., Tan, J. L. & Low, C. O. (2003). Necrotizing fasciitis: clinical presentation, microbiology, and determinants of mortality. J Bone Joint Surg Am 85, 1454–1460.
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | J MED MICROBIOL | MICROBIOLOGY | J GEN VIROL | ALL SGM JOURNALS |