J Med Cases
Journal of Medical Cases, ISSN 1923-4155 print, 1923-4163 online, Open Access
Article copyright, the authors; Journal compilation copyright, J Med Cases and Elmer Press Inc
Journal website http://www.journalmc.org

Case Report

Volume 7, Number 9, September 2016, pages 389-392


Anerobic Spondylodiscitis: A Case Report

Mohammed Kashaba, e, Mohammed Khalifaa, Hatim M. Alshareefb, Amer M. Alshareefc, Ahmed H. Alhasand

aKing Abdulaziz Medical City, Jeddah, KSA
bKing Fahd Armed Forces Hospital, Jeddah, KSA
cIbn Sina National College, Jeddah, KSA
dUniversity of Jeddah, Jeddah, KSA
eCorresponding Author: Mohammed Kashab, King Abdulaziz Medical City, Jeddah, KSA; Hatim M. Alshareef, King Fahd Armed Forces Hospital, Jeddah, KSA

Manuscript accepted for publication August 10, 2016
Short title: Anerobic Spondylodiscitis
doi: http://dx.doi.org/10.14740/jmc2629e

Abstract▴Top 

A 60-year-old female patient with a history of hypertension, diabetes mellitus, major depression, dyslipidemia, hypothyroidism, osteoarthritis and minor thalassemia on medications presented to the hospital complaining of progressive lower limb weakness over the past 10 days. An epidural injection was done as a pain control measure. She was diagnosed as anerobic spondylodiscitis. This case is unique due to the abrupt progression of the clinical picture from non to paraplegia. It is also unique in the severe destructive picture seen in the CT and MRI images done as diagnostic measures, keeping in mind that these investigations were done less than 3 weeks after the injection.

Keywords: Anerobic; Spondylodiscitis; Paraplegia

Introduction▴Top 

We report a case of anerobic spondylodiscitis that took place following an epidural injection done as a pain control measure. This case is unique due to the abrupt progression of the clinical picture from non to paraplegia. It is also unique in the severe destructive picture seen in the CT and MRI images done as diagnostic measures, keeping in mind that these investigations were done less than 3 weeks after the injection.

Case Report▴Top 

A 60-year-old lady with known conditions of hypertension, diabetes mellitus, major depression, dyslipidemia, hypothyroidism, osteoarthritis and minor thalassemia on medications presented to the hospital complaining of progressive lower limb weakness over the past 10 days. She gave a history of low back pain as a result of her prolapsed disk which was relieved by an epidural analgesic injection composed of steroid and local anesthetic in King Khalid Hospital, National Guard, Jeddah (KKH, NGHA, Jeddah) 3 weeks before her presenting illness. The injection was at the L4-L5 level. Her symptoms abruptly progressed from tingling sensations in her lower limbs until the patient completely lost motor function in both lower limbs. There was no history of trauma or constitutional symptoms. She had a neurogenic bladder at presentation.

The patient had history of previous similar epidural injections for her back pain. She had past surgical history for hernia repair. Also, she had past allergic history to penicillin and fish.

Upon admission, the patient was afebrile, and her vital signs were stable; generally she was conscious, alert, oriented and looked depressed. She was morbidly obese (BMI 51.6). Chest, cardiovascular and abdomen examinations showed no abnormality. Neurological examination showed lower limb muscle power of 0/5, absent sensation and reflexes from the T10 level and downwards. The Babinski sign was negative. There was tenderness in her back at the level of T9-T10. The admission impression was spinal cord compression secondary to epidural hematoma after the epidural analgesic injection she received.

CT was done urgently upon suspicion of post-injection hematoma. It showed no pathology at the level of injection. Rather it showed a pathological fracture at the T9-T10 level with segmental kyphosis and severe canal stenosis as shown in Figures 1 and 2. MRI images/tests indicated spondylodiscitis, cord compression and myelomalacia at T9-T10 and canal stenosis as shown in Figure 3.

Figure 1.
Click for large image
Figure 1. Pathological fracture at the T9-T10 level.

Figure 2.
Click for large image
Figure 2. Segmental kyphosis and severe canal stenosis at the T9-T10 level.

Figure 3.
Click for large image
Figure 3. Spondylodiscitis, cord compression and myelomalacia at T9-T10 with canal stenosis.

WBCs were 14.4 cells/mm3, CRP was 81.1, and ESR was 37 mm/h. A CT-guided biopsy did not demonstrate the presence of any organism but the cell count was 40,600 (86% neutrophils). The patient was put on an antibiotic regime prescribed empirically in the form of vancomycin 1 g q12h and ceftriaxone 2 g q24h. Surgery was done for the patient 4 days after admission as an urgent procedure to decompress T9, T10 with fusion and stabilization using transpedicular screws. It included multiple levels decompression with laminectomy from T6 down to T12 and posterior instrumentation.

Intraoperative findings were segmental kyphosis at the T9-T10 level with epidural fat necrosis. Upon decompressing the same level, a transpedicular biopsy showed serogenous fluid with bone debris and no pus.

There was also reactive new bone formation. There was no evidence of pus. An open biopsy for the T10 lesion was taken. Multiple samples were taken for histopathology including a dry sample, a wet sample in saline and formalin, as well as fluid for cytology. Multiple cultures were tested for aerobic and anerobic organisms, as well as TB, brucella and fungal culture.

The results of the microbiology tissue culture indicated that there was positive peptococcus infection of the vertebral bone.

After observing the offending organism and sensitivity study, the antibiotics were changed to ceftriaxone 2 g IV daily and metronidazole 500 mg IV q12h. The patient was followed up by series of blood works which demonstrated all parameters going back to normal values within a 3-month period. After 4 months period of the patient’s presentation, her motor function did not recover. A follow-up MRI was done 4 months after the surgery and it showed complete resolution of the infection and an acceptable fusion of the T9-T10 (Fig. 4).

Figure 4.
Click for large image
Figure 4. Infection and fusion at T9-T10.
Discussion▴Top 

There were no difficulties in establishing the diagnosis in our reported case. What was unique was the abrupt progression of the clinical presentation. Three scenarios were structured upon discussing this case with all concerned departments in our institute (KKH, NGHA, Jeddah); the first scenario suggests that the infection was due to contamination from the epidural injection procedure which rapidly progressed to an acute case of spondylodiscitis. The second scenario suggests that an infection was already present and subclinical before the injection of the analgesic, and that the steroid injected in the epidural space as a pain control measure reduced the immunity at that area and gave a chance for the already existent infection to flourish. The third scenario is that the peptococcus being a mouth commensal got access to the blood of the patient simultaneously as the injection was given and found the condition favorable at the demonstrated infection site due to steroids although the patient did not give any history of endodontic procedure at or shortly before the epidural injection.

Peptococcus is a gram positive coccus anerobe that is found as normal mouth commensal in the mouth of human beings. It is not pathological when in natural sites. It could be involved in tissue infection such as fasciitis and also in bone infection as demonstrated in our reported case.

The incidence of pyogenic spondylodiscitis is somewhere around 1:250,000 to 1:100,000 per annum with a mortality rate of 2-17% [1]. Pyogenic spondylodiscitis represents 2-7% of all cases of osteomyelitis [2]. The presenting symptoms are usually lower back pain with or without constitutional symptoms [3]. Lower back pain, being the most common presentation in spine clinics, may be regarded with a low suspicion index especially there are no other symptoms observed that could raise the clinician’s suspicion. All of the above mentioned factors could delay the diagnosis of this condition [4].

Once the diagnosis of spondylodiscitis is suspected attempts to isolate the causing organism should be started. Multiple blood cultures are recommended before more invasive measures are taken to isolate the causative agent [5]. In cases where blood cultures are negative then aspiration/biopsy under radiology guidance is indicated. This might not always close the case. In fact, some studies demonstrated that positive cultures from biopsy to diagnose spondylodiscitis may be as low as 32% [6].

The most frequently isolated organism in pyogenic spondylodiscitis is Staphylococcus aureus [7] and to a lesser extent streptococcus β hemolytic species. Anerobic bacteria causing spondylodiscitis are very rare [8].

MRI has a sensitivity and specificity of 96% and 94%, respectively, for diagnosing pyogenic spondylodiscitis [3, 6]. MRI should always be sought when spondylodiscitis is suspected.

Antibiotics are to be empirically started immediately upon suspension of spondylodiscitis. They should cover staphylococcus and methicillin-resistant strains [2]. After cultures and sensitivity reports are obtained, antibiotics should be changed accordingly. The optimum period of time in which to administer parenteral antibiotics is not well defined. Higher rates of failure of treatment were reported with parenteral antibiotics administration less than 4 weeks [2].

Surgical treatment might be indicated in cases of pyogenic spondylodiscitis [1]. The surgical approach usually involves debridement, sampling of the affected area for microbiological and antibiotic sensitivity study, possible decompression and possible fixation. The approach could be anterior or posterior. In our reported case, the surgical approach was posterior with fixation.

Paraplegia is reported with a prevalence of 5% in some studies [7]. In this case, the patient recovered completely in contrast to our reported case that is still paraplegic 4 months after she was diagnosed.

Conclusion

Spondylodiscitis is a poorly understood condition which may be devastating if not discovered and treated optimally. A high index of suspicion should always be present. With the advancement of invasive interventions and their increasing indications and uses, such as epidural injection, catheters, punctures, etc., strict aseptic measures should be followed. Prophylactic antibiotic administration in endodontic procedures should always be administered.


References▴Top 
  1. Zarghooni K, Rollinghoff M, Sobottke R, Eysel P. Treatment of spondylodiscitis. Int Orthop. 2012;36(2):405-411.
    doi pubmed
  2. Pola E, Logroscino CA, Gentiempo M, Colangelo D, Mazzotta V, Di Meco E, Fantoni M. Medical and surgical treatment of pyogenic spondylodiscitis. Eur Rev Med Pharmacol Sci. 2012;16(Suppl 2):35-49.
    pubmed
  3. Lee SJ, Choi EJ, Nahm FS. Spondylodiscitis after Cervical Nucleoplasty without Any Abnormal Laboratory Findings. Korean J Pain. 2013;26(2):181-185.
    doi pubmed
  4. Gurbuz MS, Berkman MZ. Spondylodiscitis occurring after diagnostic lumbar puncture: a case report. Case Rep Infect Dis. 2013;2013:843592.
  5. Aagaard T, Roed C, Dragsted C, Skinhoj P. Microbiological and therapeutic challenges in infectious spondylodiscitis: a cohort study of 100 cases, 2006-2011. Scand J Infect Dis. 2013;45(6):417-424.
    doi pubmed
  6. Sehn JK, Gilula LA. Percutaneous needle biopsy in diagnosis and identification of causative organisms in cases of suspected vertebral osteomyelitis. Eur J Radiol. 2012;81(5):940-946.
    doi pubmed
  7. Valancius K, Hansen ES, Hoy K, Helmig P, Niedermann B, Bunger C. Failure modes in conservative and surgical management of infectious spondylodiscitis. Eur Spine J. 2013;22(8):1837-1844.
    doi pubmed
  8. Saeed MU, Mariani P, Martin C, Smego RA, Jr., Potti A, Tight R, Thiege D. Anaerobic spondylodiscitis: case series and systematic review. South Med J. 2005;98(2):144-148.
    doi pubmed


This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


Journal of Medical Cases is published by Elmer Press Inc.

 

Browse  Journals  

 

Journal of Clinical Medicine Research

Journal of Endocrinology and Metabolism

Journal of Clinical Gynecology and Obstetrics

 

World Journal of Oncology

Gastroenterology Research

Journal of Hematology

 

Journal of Medical Cases

Journal of Current Surgery

Clinical Infection and Immunity

 

Cardiology Research

World Journal of Nephrology and Urology

Cellular and Molecular Medicine Research

 

Journal of Neurology Research

International Journal of Clinical Pediatrics

 

 
       
 

Journal of Medical Cases, monthly, ISSN 1923-4155 (print), 1923-4163 (online), published by Elmer Press Inc.                     
The content of this site is intended for health care professionals.
This is an open-access journal distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, which permits unrestricted
non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Creative Commons Attribution license (Attribution-NonCommercial 4.0 International CC-BY-NC 4.0)


This journal follows the International Committee of Medical Journal Editors (ICMJE) recommendations for manuscripts submitted to biomedical journals,
the Committee on Publication Ethics (COPE) guidelines, and the Principles of Transparency and Best Practice in Scholarly Publishing.

website: www.journalmc.org   editorial contact: editor@journalmc.org
Address: 9225 Leslie Street, Suite 201, Richmond Hill, Ontario, L4B 3H6, Canada

© Elmer Press Inc. All Rights Reserved.


Disclaimer: The views and opinions expressed in the published articles are those of the authors and do not necessarily reflect the views or opinions of the editors and Elmer Press Inc. This website is provided for medical research and informational purposes only and does not constitute any medical advice or professional services. The information provided in this journal should not be used for diagnosis and treatment, those seeking medical advice should always consult with a licensed physician.