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Brucella infection of the thoracic vertebral arch presenting with an epidural abscess: a case report
© Yin et al. 2015
Received: 22 March 2015
Accepted: 25 September 2015
Published: 23 October 2015
Although Brucella spondylitis and Brucella discitis have been frequently reported, Brucella infection of the vertebral arch is rare and has not been previously described. We present the first case of Brucella infection of the thoracic vertebral arch with epidural abscess formation and discuss the clinical key points.
A 57-year-old man of Han nationality with a history of contact with an isolated sheep stomach 2 months previously was admitted with an undulant fever, night sweats, back pain, and weakness. Thoracic magnetic resonance imaging showed laminar destruction of T9 and an epidural abscess at the T9 to 10 level with significant cord compression. Diagnosis of Brucella infection of his vertebral arch was confirmed by a positive blood culture with growth of Brucella melitensis. Total laminectomy, abscess cleansing, and percutaneous pedicular screw fixation was performed initially, followed by antibiotic treatment with a combination of doxycycline and rifampin for 4 months. Recovery was confirmed by clinical, magnetic resonance imaging, and blood culture findings.
This is an unusual case of Brucella infection of the vertebral arch with epidural abscess formation. Effective antibiotic therapy of a sufficient duration and timely performance of surgical treatment are the key points in management of such cases.
Brucellosis is an endemic and systemic disease with characteristic symptoms of undulant fever, night sweats, and weakness . It can involve any organ or tissue, including the eyes, liver, lungs, nervous system, cardiovascular system, bone, and joints . Localized brucellosis most commonly involves the bones and joints (10 to 80 % of cases) [1, 3], especially the axial skeleton, and results in Brucella spondylitis, sacroiliitis, and peripheral arthritis. In the spine, the vertebral bodies and intervertebral disk areas are the most frequently affected sites , and Brucella spondylitis or discitis with epidural abscess formation has been frequently reported [4, 5]. However, the posterior arch of the vertebra is rarely involved, and no such cases have been reported.
We present an unusual case of brucellosis with neural arch infection and epidural abscess formation at the thoracic level. The case is special not only because brucellosis involving the posterior arch of the vertebra is rare, but also for the different pathological changes and operative methods.
After 1 day of preoperative preparation, he underwent total laminectomy at T8 to 10 with percutaneous pedicle screw fixation at T7 to 8 and T11 to 12. The abscess and lesion (composed of sequestrum fragments, inflammatory granulation tissue, and smaller separate abscesses) were removed after collecting samples for pathology and culture. Chronic nonspecific inflammation was detected in the biopsy sample, and no bacteria grew in the culture. One day after the operation, the previously cultured Gram-negative bacillus from his blood was identified as Brucella melitensis, and a with minimal inhibitory concentration (MIC) of 0.094ug/ml, and rifampin was also sensitive with 26 in Kirby–Bauer (KB) method. Thus, he was finally diagnosed with Brucella infection of the thoracic vertebral arch with epidural abscess formation. He received antibiotic therapy with cefoperazone sodium and sulbactam sodium (1.5g twice daily, since admission) administered intravenously for 4 weeks and antibiotic therapy with doxycycline (100mg twice daily) and rifampin (450mg once daily) administered orally for 4 months according to the drug sensitivity test. After this treatment, his recovery was confirmed by clinical findings (disappearance of night sweats, weakness, and fever), laboratory test results (three negative blood cultures), and MRI findings (adequate decompression, no abscesses, and no inflammatory reaction in his spine). He was discharged 4 weeks after the operation and followed up in our out-patient clinic for 10 months with no evidence of disease recurrence. He has also been followed up in the Epidemic Prevention Station of Guangzhou city; the Rose Bengal test was negative in his serum three times together with a tube agglutination titer of 1/24.
Brucellosis is an endemic and zoonotic disease caused by Gram-negative bacteria of the genus Brucella . Brucella species are transmitted directly or indirectly from infected animals to humans. The genus Brucella was first discovered by David Bruce in 1887 . Since the report of human brucellar spondylitis by Kulowski and Vinke in 1932 , there have been several case reports about spinal brucellar infection. In 1987, Goodhart et al.  reported the case of a patient with spinal brucellosis with bilateral paraspinal abscesses. Subsequently in 1999, Pina et al.  presented a case of Brucella spondylodiscitis and an epidural abscess in the cervical spine. That same year, Bingol et al.  presented a case of a thoracic intramedullary Brucella granuloma that was resolved by medication. In 2000, Zormpala et al.  reported a case of Brucella spondylitis involving both the cervical and lumbar spine. In 2007, Cobbaert et al.  encountered an uncommon case of Brucella spondylodiscitis in the lumbar spine in a patient with abdominal pain. Also in 2007, Nas et al.  were the first to report a case of an intramedullary Brucella granuloma in the cervical spine. Finally, in 2010, Yilmaz et al.  described a patient with a lumbar disc herniation caused by Brucella discitis. Approximately 500,000 cases of brucellosis are reported annually worldwide, most of which occur in developing countries [1, 2]. Although there were lots of reports about brucellar infection involving the vertebral body or intervertebral disc, there was no previous report about brucellar infection involving the vertebral arch.
The diagnosis of spinal brucellosis is mainly confirmed by clinical features, imaging examination of the spine, and laboratory findings of brucellosis (positive serum agglutination and/or blood culture) . In the present case, the clinical features were obvious with undulant fever, night sweating, back pain, progressive weakness, and hypermyotonia in both legs. CT and MRI revealed a laminar osteolytic focus and inflammatory reaction in T9 and an epidural abscess with significant cord compression between T9 and 10. A blood culture was positive for B. melitensis.
This specific case of neural arch brucellosis was treated similar to other types of spinal brucellosis with a good outcome. Antibiotic treatment is one of the keypoints in dealling with brucellosis; the most common antibiotic treatment is a combination of doxycycline (100mg every 12 hours orally) and rifampicin (600 to 900mg/day orally) for 8 weeks or more . Many researchers have emphasized that the duration of antibiotic therapy should be based on the patient’s individual condition and the extent of the lesions [4, 5, 15]. Postoperatively, our patient was cured by a combination of doxycycline (100mg every 12 hours orally) and rifampicin (600mg/day orally) for 8 weeks, and no relapse was detected in follow-ups over 1 year. In this case, Sulperazone (sulbactam and cefoperazone) was used for 4 weeks after admission, at the sixth day of using Sulperazone (sulbactam and cefoperazone) the fever was controlled so we believed that Sulperazone (sulbactam and cefoperazone) is sensitive in brucellar infection. Unfortunately, Sulperazone (sulbactam and cefoperazone) was not included in the drug sensitivity test.
The need for a surgical operation in patients with spinal brucellosis  is considered in cases of spinal instability, cord compression, radiculopathy, cauda equina syndrome, and epidural abscess formation. Surgical intervention was performed in this patient to treat cord compression caused by the epidural abscess. On intraoperative examination we found many small abscesses separated by fibrous granulation tissue; however, no dissociative sequestra were found in either the abscess or fibrous granulation tissue, differentiating it from spinal tuberculosis.
This study has two notable limitations. The most significant is the lack of serous agglutination in the first 3 months of the patient’s clinical course of illness. In addition, the follow-up period was short; longer observation periods are needed to definitively exclude the presence of recurrence.
This case of Brucella infection of the vertebral arch with epidural abscess formation is unusual. Effective antibiotic therapy for a sufficient duration and timely performance of surgery are the key points to consider in managing such cases. We believe that Sulperazone (sulbactam and cefoperazone) is sensitive in brucellar infection.
I have no medical knowledge about my case and only write from my own perspective and experience to provide assistance to the case report.
When I was 57 years of age, I had a full-time job at a private enterprise. I believed that I was in very good health; I had never been admitted to hospital for any problems. However, on one afternoon last summer I became very exhausted and hot. I thought I must have had influenza, so I drank more water than usual, rested in bed, and took Bufferin (aspirin) twice a day. When I awoke the next morning I no longer felt hot, but instead experienced cool sweats. That afternoon I felt worse and went to see a doctor in a traditional Chinese medicine hospital in Guangzhou. A nurse took my temperature, which was 38.7 °C, and introduced me to the doctor. The doctor asked me if I had a headache or backache. I said yes and felt very tired. After a routine blood test I was determined to have a fever of unknown origin and was given cefprozil tablets and treatment with traditional Chinese medicine. A nurse gave an injection in my arm, but I don’t know what the injection was. Whatever it was, it relieved the fever instantly. I followed the prescribed therapy at home for nearly 1 month, but still ran a temperature, although it was below 38 °C most afternoons; it was relieved at night. The therapy did not seem to be effective; my backache worsened, I developed progressive weakness, and I had a slight cough. Therefore, I visited a professor in the Department of Respiration of the First Affiliated Hospital of Guangzhou Medical University. He presumed that I may have tuberculosis and advised me to undergo further testing and treatment in his hospital.
I was admitted to the hospital in June 2014. They asked me if I had been in contact with any people with tuberculosis; I said no, there was little chance of this. They then asked me if I had been in contact with any animals. I remembered that I had touched the isolated stomach of a sheep with my injured hand about 1 month previously. Many blood tests and some X-rays, CT, and MRI were performed, and intravenous infusions and antibiotics were administered. I didn’t run a fever for 5 days after admission, but I felt weak and numb in both legs, and it was difficult to walk and urinate. On the sixth day after admission, I was informed that MRI showed evidence of a specific infection in the thoracic spine, and I was transferred to the Department of Orthopaedic Surgery the next day. An operation was performed 8 days after admission. The next day I was diagnosed with brucellosis based on a positive blood culture and treated with doxycycline and rifampin for at least 4 months.
After nearly a month of hospitalization, I spent approximately 4 months taking oral antibiotics at home with doxycycline and rifampin. Three months after leaving the hospital, I had a good appetite for strongly flavored food, no longer felt tired, and experienced no further night sweats. During this period, I underwent blood cultures and agglutination tests three times, and all results were negative. I underwent another MRI examination in September, and no compression or abscesses were detected in my spine. My doctor informed me that I had completely recovered. I felt fully back to health and had returned to work by the end of October. After a further 8 months of follow-up, I had no evidence of recurrence.
Written informed consent was obtained from our patient for the publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
The authors thank Dr Chunli Liu from the Department of Respiration for providing diagnostic evidence (positive blood culture) and contributing to the therapeutic strategy of the case.
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