<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJMN</journal-id><journal-title-group><journal-title>Open Journal of Modern Neurosurgery</journal-title></journal-title-group><issn pub-type="epub">2163-0569</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojmn.2019.93031</article-id><article-id pub-id-type="publisher-id">OJMN-93996</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Acute Paraplegia Due to &lt;i&gt;Salmonella brandenburg&lt;/i&gt; Spondylodiscitis: Case Report
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Claudiu</surname><given-names>Popa</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Maguette</surname><given-names>Mbaye</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mbaye</surname><given-names>Thioub</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Tanguy</surname><given-names>Riem</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Benjamin</surname><given-names>Daumas-Duport</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Nathalie</surname><given-names>Asseray</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Roger</surname><given-names>Robert</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib></contrib-group><aff id="aff5"><addr-line>Department of Infectious Diseases, CHU Nantes, Nantes, France</addr-line></aff><aff id="aff4"><addr-line>Department of Neuroradiology, CHU Nantes, Nantes, France</addr-line></aff><aff id="aff1"><addr-line>Department of Neurosurgery, CHU Saint Etienne, Saint Etienne, France</addr-line></aff><aff id="aff2"><addr-line>Department of Neurosurgery, CHNU Fann, Dakar, Sénégal</addr-line></aff><aff id="aff3"><addr-line>Department of Neurosurgery, CHU Nantes, Nantes, France</addr-line></aff><pub-date pub-type="epub"><day>08</day><month>05</month><year>2019</year></pub-date><volume>09</volume><issue>03</issue><fpage>327</fpage><lpage>337</lpage><history><date date-type="received"><day>1,</day>	<month>March</month>	<year>2019</year></date><date date-type="rev-recd"><day>3,</day>	<month>April</month>	<year>2019</year>	</date><date date-type="accepted"><day>30,</day>	<month>July</month>	<year>2019</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  The authors present the case of a 48-year-old man admitted for acute onset of paraplegia in a patient suffering from backaches for 1 week. The rapidly progressive motor disturbances had been evolving for approximately 12 hours. The entire spinal MRI showed an epidural mass at T4-T6 associated with extensive lesions of spondylodiscitis and a T7-T8 vertebral body loss of height. A large six-level laminectomy was performed. A tumoral etiology couldn’t be entirely excluded intraoperatively so that no fusion has been done at that time. The pathological exam revealed acute inflammatory lesions with no argument in favor of a tumoral process. Bacteriological exam of the pathological specimen and stools cultures were positive for 
  <em>Salmonella brandenburg</em>. An episode of gastroenteritis after the ingestion of a pizza has been evoked. The antibiotic medication was prescribed for 12 weeks. Postoperative evolution was favorable with a possible march between bars 6 weeks after. The authors emphasize the pseudo-tumoral presentation in an immunocompetent patient, the lack of complications and the post-ingestion mechanism.
 
</p></abstract><kwd-group><kwd>Spondylodiscitis</kwd><kwd> Spinal Epidural Abscess</kwd><kwd> Paraplegia</kwd><kwd> &lt;i&gt;Salmonella brandenburg&lt;/i&gt;</kwd><kwd> Post-Ingestion</kwd><kwd> Immunocompetent</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Background. Infections of the spine are still being described in medical literature as spondylitis, discitis, vertebral osteomyelitis, septic arthritis of the facet joints, spondylodiscitis (SD) and/or spinal epidural abscess (SEA). Terms as pyogenic and hematogenous are often added with claimed intention to point out the non-specific infectious character and, respectively, the most frequently encountered modality of spreading. Also, the term spontaneous is mostly reserved for infections other than post-surgical. The presence or the absence of a spinal epidural abscess could bring out a spinal cord compression which constitutes a neurosurgical emergency. That’s why, for more practical reasons, we should classify spinal infections in spondylodiscitis (or vertebral osteomyelitis) with or without spinal epidural abscess.</p><p>SD accounts for 2% of bony infections [<xref ref-type="bibr" rid="scirp.93996-ref1">1</xref>] . SEA comprises for 0, 2-2 cases for 10,000 hospital admissions [<xref ref-type="bibr" rid="scirp.93996-ref2">2</xref>] .</p><p>Age. SEA occurs in patients aged 30 - 60 and two times more frequently in men [<xref ref-type="bibr" rid="scirp.93996-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref5">5</xref>] . Elderly people are more susceptible to developing SD [<xref ref-type="bibr" rid="scirp.93996-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref7">7</xref>] .</p><p>Level. The lumbar spine is affected in 50% of cases with SD [<xref ref-type="bibr" rid="scirp.93996-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref10">10</xref>] . The thoracic level was reported in over 50% of cases with SEA, followed by lumbar, then cervical [<xref ref-type="bibr" rid="scirp.93996-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref11">11</xref>] , with a prevalence of midthoracic spine (T6-T8) [<xref ref-type="bibr" rid="scirp.93996-ref12">12</xref>] . SEA appears more frequently in the cervical spine (90%) upon certain authors [<xref ref-type="bibr" rid="scirp.93996-ref13">13</xref>] , or lumbar spine in another series [<xref ref-type="bibr" rid="scirp.93996-ref4">4</xref>] but causes a neurological deficit in the thoracic spine (80%) [<xref ref-type="bibr" rid="scirp.93996-ref13">13</xref>] . Over 80% are posterior to the cord [<xref ref-type="bibr" rid="scirp.93996-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref14">14</xref>] .</p><p>The lumbar spine seems to be more affected by Salmonella infection [<xref ref-type="bibr" rid="scirp.93996-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref19">19</xref>] . Some authors claim that thoracic SD with Salmonella in immunocompetent patients is extremely rare [<xref ref-type="bibr" rid="scirp.93996-ref20">20</xref>] .</p></sec><sec id="s2"><title>2. Case Report</title><p>A 48-year-old man, with no significant history, has been admitted in the Neurosurgical Emergency Room for acute onset of paraplegia for approximately 12 hours. He had been experiencing progressively increasing backaches for over a week and that morning he awoke noticing he couldn’t move his legs. He saw his general doctor and he had been prescribed non-steroidal anti-inflammatory drugs. Examination revealed a 0/5 paraplegia with loss of bladder and bowel function and a sensory level at T8. No fever was noted. Radiographic studies showed an extended T4-T7 area of osteolysis and a T7-T8 vertebral body loss of height. Preliminary laboratory exams showed a white blood cell count (WBC) at 10.600/ml, fibrinogen at 6.9 g/l, platelets at 161.000/ml and TCA ratio at 1.35. Blood cultures remained negative the whole course of hospitalization. MRI showed T6-T7-T8 vertebral body and discal lesions with an epidural mass at T4-T6 with a compressive effect on the spinal cord and bone marrow signal intensity abnormalities (<xref ref-type="fig" rid="fig1">Figure 1</xref>). He underwent emergent T3-T8 laminectomy and an easily aspirating, greyish/yellowish mass with a purulent liquid at the superior part has been noticed. The relative spinal stability and the tumor-evoking MRI aspect determined us to perform no fusion at that time. The pathological exam revealed an inflammatory, neutrophilic infiltrated adipose tissue with no arguments for a tumoral primitive or metastatic process. Bacteriological specimen exam and stool cultures were, somehow unexpectedly, positive for Salmonella brandenburg. The patient’s last two-week history revealed an episode of gastroenteritis after the ingestion of a pizza. Antibiotics were prescribed (Rocephin 2 g QD and Tavanic 500 mg QD prior to antibiogram, Tavanic 500 mg QD and Cotrimoxazole BID after obtaining the antibiogram) for 3 months. Immobilization was realized with a thoracolumbar orthosis for 3 months. HIV/AIDS test was negative. Thoracic and abdominal CAT scan showed no evidence of mycotic aortic aneurysm or other infectious foci. Postoperative anemia was due to intra-operative blood loss. Biological exams showed a decrease of C-reactive protein (CRP) from 51.9 mg/l to 5.3 mg/l (normal values &lt; 6 mg/l) at 3 weeks postoperatively. Clinical evolution was favorable, with a 3/5 paraparesis and a caned-march at 6 weeks. He had a urethral sonde at discharge. An MRI performed 4 weeks after the operation showed the resolution of pyogenic lesions (<xref ref-type="fig" rid="fig2">Figure 2</xref>). The patient was discharged 7 weeks later for a re-educational hospital.</p></sec><sec id="s3"><title>3. Discussion</title><p>Presentation: Spondylodiscitis associated with a SEA is difficult to recognize disease since the presentation is non-specific [<xref ref-type="bibr" rid="scirp.93996-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref22">22</xref>] . Medical literature reveals high rates of inaccurate first-time diagnosis. A 40-cases retrospective series reports over 25% of misdiagnosed and discharged patients with SEA [<xref ref-type="bibr" rid="scirp.93996-ref23">23</xref>] . For Tang et al. the initial accurate diagnostic rate was 11% [<xref ref-type="bibr" rid="scirp.93996-ref24">24</xref>] .</p><p>Clinical presentation like back pain, fever, local signs and/or neurological impairment associated with an inflammatory syndrome (CRP, WBC, ESR) point out a possible spinal infection [<xref ref-type="bibr" rid="scirp.93996-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref24">24</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref26">26</xref>] . Meningismus may be also associated [<xref ref-type="bibr" rid="scirp.93996-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref27">27</xref>] . Paralysis appears in 34% of cases with SEA [<xref ref-type="bibr" rid="scirp.93996-ref2">2</xref>] .</p><p>Fever is absent in one-third of the patients [<xref ref-type="bibr" rid="scirp.93996-ref2">2</xref>] . In fact, some authors claim that spondylodiscitis without fever is a diagnostic challenge and they conclude that spondylodiscitis should always be considered when the differential diagnosis is made [<xref ref-type="bibr" rid="scirp.93996-ref28">28</xref>] . Some series of patients with Salmonella spondylodiscitis reported the presence of back pain in 100% of cases and fever in 75% [<xref ref-type="bibr" rid="scirp.93996-ref29">29</xref>] .</p><p>History of more than 3 months of symptoms is present in 50% of cases [<xref ref-type="bibr" rid="scirp.93996-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref9">9</xref>] .</p><p>Our patient’s presentation was unusual for he had no fever or local signs at the time of admittance and he had been experiencing backaches for only a week. His immunologic condition seemed normal since his medical history was insignificant. His minimal leucocytosis (10.600/ml) and the moderate rise of fibrinogen (6.9 g/l) could be hardly interpreted as specific signs of infection. Also, leucocytosis correlated with lytic lesions on radiographic studies could point out a neoplasia condition. Negative blood cultures added no argument for a spinal infection.</p><p>MRI: Plain radiographs may reveal vertebral body collapse and lytic lesions within the vertebral body or posterior spinal elements [<xref ref-type="bibr" rid="scirp.93996-ref4">4</xref>] . MRI is the golden standard nowadays [<xref ref-type="bibr" rid="scirp.93996-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref30">30</xref>] , though CT-scan, scintigram and plain X-rays may be helpful [<xref ref-type="bibr" rid="scirp.93996-ref4">4</xref>] . Typical MRI characteristics of SEA, disc and involved vertebral bodies are heterogeneous iso/hypointense on T1-weighted images and hyperintense on T2-weighted images [<xref ref-type="bibr" rid="scirp.93996-ref22">22</xref>] . Inhomogeneous enhancement of disc-vertebral body complex following contrast administration is usually seen on T1-weighted images [<xref ref-type="bibr" rid="scirp.93996-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref31">31</xref>] . Pronounced peripheral enhancement orientates the diagnosis toward an abscess rather than a cystic lesion (old hematoma or serum) [<xref ref-type="bibr" rid="scirp.93996-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref31">31</xref>] . Signal changes of the vertebral body bone marrow can be seen either in infectious or neoplastic diseases of the spine. Differential diagnosis should be made with leptomeningeal metastases [<xref ref-type="bibr" rid="scirp.93996-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref27">27</xref>] , epidural hematoma [<xref ref-type="bibr" rid="scirp.93996-ref14">14</xref>] , meningitis, acute transverse myelitis, inter somatic herniation [<xref ref-type="bibr" rid="scirp.93996-ref11">11</xref>] , multiple myeloma or other hematologic neoplasia, vertebral body collapse followed osteoporosis [<xref ref-type="bibr" rid="scirp.93996-ref9">9</xref>] .</p><p>Treatment. Treatment can be either conservative (antibiotics and/or immobilisation) or surgical (especially with neurological impairment) [<xref ref-type="bibr" rid="scirp.93996-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref32">32</xref>] . Neurosurgical indications in spinal infections are a diagnostic biopsy, progressive neurologic deficit, spinal instability and failed medical response [<xref ref-type="bibr" rid="scirp.93996-ref12">12</xref>] .</p><p>Still, no consensus exists in literature concerning indication for surgical treatment for spinal infections. In one series, 90% of patients with SD were treated effectively by non-surgical means [<xref ref-type="bibr" rid="scirp.93996-ref33">33</xref>] . A complete paralysis for more than 3 days seems to be a specific criterion for conservative therapy [<xref ref-type="bibr" rid="scirp.93996-ref34">34</xref>] . SD medical treatment with immobilization and antibiotics would permit 75% pain relief and spontaneously fusion [<xref ref-type="bibr" rid="scirp.93996-ref4">4</xref>] . The use of a thoracolumbosacral orthosis was evoked by certain authors as external stabilization [<xref ref-type="bibr" rid="scirp.93996-ref9">9</xref>] . On the other hand, in a study of 75 patients with SEA, Rigamonti et al. conclude that conservative treatment seems to be reserved for selective cases [<xref ref-type="bibr" rid="scirp.93996-ref26">26</xref>] .</p><p>The main treatment of SEA seems to be early surgery [<xref ref-type="bibr" rid="scirp.93996-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref23">23</xref>] . Primary instrumentation may be considered [<xref ref-type="bibr" rid="scirp.93996-ref9">9</xref>] . There is no consensus among authors for the use of a certain type of surgery or for immediate fusion [<xref ref-type="bibr" rid="scirp.93996-ref35">35</xref>] . In a study of 163 patients, Karadimas et al. found that decompression alone was less effective compared with decompression and internal stabilization [<xref ref-type="bibr" rid="scirp.93996-ref33">33</xref>] . The use of metallic implants was reported successful in all 22 patients with spondylodiscitis by Robinson et al. [<xref ref-type="bibr" rid="scirp.93996-ref36">36</xref>] . The use of immediate internal fusion, with better materials and broad-spectrum antibiotics, would allow early mobilization, thus avoiding complications such as deep vein thrombosis [<xref ref-type="bibr" rid="scirp.93996-ref7">7</xref>] . Nevertheless, Bostrom et al., in a study of 46 patients with SEA concluded that instrumentation does not seem to be imperative [<xref ref-type="bibr" rid="scirp.93996-ref37">37</xref>] . Nakase et al. reported two-stage surgical management of their patients [<xref ref-type="bibr" rid="scirp.93996-ref38">38</xref>] . On a technical note, Greiner-Perth et al. present their good results with the use of a less invasive surgical approach of SEA [<xref ref-type="bibr" rid="scirp.93996-ref39">39</xref>] .</p><p>The use of an anterior or posterior approach is still controversial. Many authors prefer the anterior approach [<xref ref-type="bibr" rid="scirp.93996-ref7">7</xref>] , though the posterior approach seems more logical since 80% of SEA are dorsally situated [<xref ref-type="bibr" rid="scirp.93996-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref21">21</xref>] . However, the posterior approach would bear the risk of postoperative instability. The use of intraoperative sonography and a drainage system are also debated [<xref ref-type="bibr" rid="scirp.93996-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref34">34</xref>] . The risk of congestion of irrigation fluid is cited [<xref ref-type="bibr" rid="scirp.93996-ref21">21</xref>] .</p><p>Some authors cite the postoperative complication rate of 33% [<xref ref-type="bibr" rid="scirp.93996-ref12">12</xref>] .</p><p>In our case, we chose the posterior approach since the SEA was posterior. Imagistic preoperative and intraoperative criteria of spinal stability determined us to consider fusion as not necessary at that moment. Moreover, we think that an external stabilization should be firstly considered in such cases. Immediate postoperative evolution and pathological and bacteriological exams will dictate an eventual second-time fusion.</p><p>Antibiotics: The period of time for antibiotic therapy is between 4 - 6 weeks [<xref ref-type="bibr" rid="scirp.93996-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref28">28</xref>] to 3 months [<xref ref-type="bibr" rid="scirp.93996-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref40">40</xref>] and should comprise a period of 4 - 6 weeks of parenteral administration [<xref ref-type="bibr" rid="scirp.93996-ref12">12</xref>] . Diagnosis should be confirmed by direct exam [<xref ref-type="bibr" rid="scirp.93996-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref27">27</xref>] or blood culture before prescribing antibiotics [<xref ref-type="bibr" rid="scirp.93996-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref28">28</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref40">40</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref41">41</xref>] (nevertheless up to 50% of cultures are negative) [<xref ref-type="bibr" rid="scirp.93996-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref21">21</xref>] . The treatment with Quinolone is considered by a great majority of authors the best for spinal infections with Salmonella [<xref ref-type="bibr" rid="scirp.93996-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref32">32</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref42">42</xref>] .</p><p>In our case, we used a combination of a quinolone with a sulfonamide (Levofloxacin-Cotrimoxazole) and we considered that a minimum period of three months would be necessary. CRP levels and clinical evolution will be followed and antibiotic therapy will be modified accordingly.</p><p>Salmonella brandenburg: The most popular germ is by far Staphylococcus aureus, comprising for 40% - 80% of infections [<xref ref-type="bibr" rid="scirp.93996-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref26">26</xref>] , followed by other Gram-positive cocci (Streptococcus) [<xref ref-type="bibr" rid="scirp.93996-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref26">26</xref>] . Gram-negative organisms, such as Escherichia coli, Pseudomonas, Proteus, Diplococcus pneumoniae, Serratia, Enterobacter, and Salmonella seem to have an increasing incidence, especially due to IV drug use [<xref ref-type="bibr" rid="scirp.93996-ref4">4</xref>] . Also, spinal infections with anaerobic bacteria (Bacteroides, Peptostreptococcus), fungi and parasites have been cited [<xref ref-type="bibr" rid="scirp.93996-ref10">10</xref>] .</p><p>The most common Salmonella serotypes were: S choleraesuis C1 [<xref ref-type="bibr" rid="scirp.93996-ref29">29</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref43">43</xref>] , S typhimurium and S enteriditis [<xref ref-type="bibr" rid="scirp.93996-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref19">19</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref42">42</xref>] , S paratyphi B [<xref ref-type="bibr" rid="scirp.93996-ref44">44</xref>] , S typhi [<xref ref-type="bibr" rid="scirp.93996-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref32">32</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref45">45</xref>] .</p><p>In a study of 151 patients, Ben Taarit et al. found that Salmonella was the third cause of pyogenic SD, following Staphylococcus and Brucella [<xref ref-type="bibr" rid="scirp.93996-ref6">6</xref>] , whereas Maiuri et al. reported Salmonella as the fourth cause of SD in a study of 65 patients [<xref ref-type="bibr" rid="scirp.93996-ref1">1</xref>] .</p><p>In a similar case report, Abdullah et al. present a thoracic SEA caused by Salmonella Typhi in a patient suffering from diabetes mellitus, with a skin infection. Favorable outcome was obtained after early surgery and antibiotic therapy (Ceftriaxone and Ciprofloxacin) [<xref ref-type="bibr" rid="scirp.93996-ref45">45</xref>] .</p><p>Perras et al. report the case of a 59-year-old man who developed Salmonella enteritidis SD 4 weeks after bronchopneumonia and was treated with antibiotics for 3 months (Ciprofloxacin) [<xref ref-type="bibr" rid="scirp.93996-ref46">46</xref>] .</p><p>Liu et al. present the case of a 60-year-old woman who developed a thoracic SD with Salmonella choleraesuis, treated successfully with antibiotics (ceftriaxone) after percutaneous transpedicular biopsy, in spite of a 4/5 graded lower limbs weakness at admittance [<xref ref-type="bibr" rid="scirp.93996-ref47">47</xref>] .</p><p>&#214;zturk et al. present the case of a 53-year-old woman under immunosuppressive treatment who developed a thoracic Salmonella typhimurium SEA 2 month after laparoscopic cholecystectomy. Treatment consisted of anterior and posterior fusion after decompression and antibiotic therapy (Ciprofloxacin) for 6 weeks followed by complete recovery 15 months later [<xref ref-type="bibr" rid="scirp.93996-ref16">16</xref>] .</p><p>We can conclude that the SEA with Salmonella seems to be more frequent in aged and/or immunosuppressed patients [<xref ref-type="bibr" rid="scirp.93996-ref48">48</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref49">49</xref>] .</p><p>Spreading. The most common is hematogenous spreading from various foci: skin, parenteral, urinary tract, endocarditis, respiratory or upper digestive systems [<xref ref-type="bibr" rid="scirp.93996-ref35">35</xref>] , the arterial spread being more frequent than venous transmission [<xref ref-type="bibr" rid="scirp.93996-ref9">9</xref>] . The latter is implied in genitourinary or gastrointestinal prior infections, posterior elements of the spine being mostly implicated [<xref ref-type="bibr" rid="scirp.93996-ref10">10</xref>] . Direct extension, post-operative and trauma are other mechanisms of transmission, though no source can be identified in up to 50% [<xref ref-type="bibr" rid="scirp.93996-ref11">11</xref>] . Pathogenesis of the neurologic deficits comprises a mechanical factor (compression of a SEA, the collapse of the vertebral body), an ischemic factor (decreased arterial flow, venous stasis due to local thrombosis) and a toxic factor (inflammatory products) [<xref ref-type="bibr" rid="scirp.93996-ref22">22</xref>] , the first being considered the most important [<xref ref-type="bibr" rid="scirp.93996-ref21">21</xref>] .</p><p>Postingestion: The prior digestive signs seem non-specific for the infection with Salmonella. In fact, in certain series of spondylodiscitis with Salmonella, gastrointestinal symptoms were completely absent [<xref ref-type="bibr" rid="scirp.93996-ref29">29</xref>] . Further, the post-ingestion mechanism appears to be very rarely encountered in literature. Our patient’s gastroenteritis and positive stool cultures for Salmonella point out ingestion as the probable mechanism of infection. Consequently, venous spreading through Batson’s valveless epidural venous plexus seems to be more probable.</p><p>Immunologic condition, Co-morbidities. A large consensus among authors states that spinal infections are associated with chronic diseases in up to 65%. Conditions like diabetes mellitus, IV drug abuse, advanced age, cancer, alcoholism, liver cirrhosis, HIV/AIDS, chronic renal failure, repeated urinary tract infections, medical acts will compromise immunity and will favor the development of infection [<xref ref-type="bibr" rid="scirp.93996-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref14">14</xref>] . Many authors found a frequent association of SD with aortic aneurysms [<xref ref-type="bibr" rid="scirp.93996-ref29">29</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref50">50</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref51">51</xref>] , sickle-cell disease [<xref ref-type="bibr" rid="scirp.93996-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref26">26</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref44">44</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref52">52</xref>] or systemic leptospirosis [<xref ref-type="bibr" rid="scirp.93996-ref49">49</xref>] . SEA—mycotic aortic aneurysm association seems to affect especially aged, immuno-depressed patients, being highly lethal [<xref ref-type="bibr" rid="scirp.93996-ref50">50</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref53">53</xref>] , whereas SD—sickle-cell disease association appears more frequent in the pediatric population [<xref ref-type="bibr" rid="scirp.93996-ref54">54</xref>] . Some authors state that routine echocardiography should be implied in infections with Staphylococcus or Streptococcus [<xref ref-type="bibr" rid="scirp.93996-ref40">40</xref>] .</p><p>In a review of 44 patients of Salmonella SD, Santos and Sapico found that fever was present in 87%, blood cultures were positive in 48% of cases and mycotic aortic aneurysms were seen in the over 50-year-old group [<xref ref-type="bibr" rid="scirp.93996-ref51">51</xref>] . In a series of 8 patients with Salmonella SD, 2 had concomitant mycotic aortic aneurysm [<xref ref-type="bibr" rid="scirp.93996-ref29">29</xref>] . Among the germs that provoke SD, Salmonella is the most common cause of mycotic aortic aneurysm [<xref ref-type="bibr" rid="scirp.93996-ref53">53</xref>] . Among Salmonella serotypes, S. typhi and S. choleraesuis are the most common species associated with mycotic aortic aneurysms [<xref ref-type="bibr" rid="scirp.93996-ref50">50</xref>] . Chen SH et al. report 3 cases of S. choleraesuis and 1 case of S. enteritidis SD associated with mycotic aortic aneurysm [<xref ref-type="bibr" rid="scirp.93996-ref53">53</xref>] .</p><p>No complications were described in our case probably due to the patient’s age and prior good condition. A thoracolumbar CT-scan revealed no aortic aneurysmal lesion. The early surgical decompression (within 18 hours) and the targeted antibiotics therapy permitted a favorable evolution.</p><p>Outcome. Favorable in spondylodiscitis with variable reports concerning pain-free rate (25% - 100%) [<xref ref-type="bibr" rid="scirp.93996-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref11">11</xref>] . Outcome may be fatal in approximately 6% - 20% of the patients with SEA [<xref ref-type="bibr" rid="scirp.93996-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref37">37</xref>] . Morbidity rates are very high in patients with previous neurological deficits (even for those operating within 12 hours of onset) and depend on early diagnosis [<xref ref-type="bibr" rid="scirp.93996-ref22">22</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref23">23</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref25">25</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref43">43</xref>] . In a study of 101 patients with spinal infection, 23% of patients recovered completely after surgical treatment [<xref ref-type="bibr" rid="scirp.93996-ref13">13</xref>] . In another study of 24 cases, 8 from 13 patients with neurological deficits never recovered [<xref ref-type="bibr" rid="scirp.93996-ref7">7</xref>] . In a study of 27 cases of SEA, the 3 primary paraplegic patients never improved. The authors concluded that thoracic localization has the poorest outcome [<xref ref-type="bibr" rid="scirp.93996-ref21">21</xref>] . However, complete recovery after paraplegia remains possible [<xref ref-type="bibr" rid="scirp.93996-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.93996-ref22">22</xref>] .</p><p>Our patient’s short follow-up doesn’t allow us to formulate definitive conclusions concerning his neurological evolution. Two months after the intervention his motor, sensorial and bowel disturbances improved (3/5 paraparesis, walk with walking sticks and an external anal sphincter control) but bladder dysfunctions remained unchanged.</p></sec><sec id="s4"><title>4. Conclusion</title><p>Spinal epidural abscess (SEA) is an uncommon disease. Symptoms involve a classic triad of fever, backache and neurological deficits but all the symptoms are rarely seen at the first contact. The treatment of SEA involves emergent laminectomy, drainage of the abscess and antibiotic therapy. Prompt diagnosis and early surgical intervention, are associated with a favorable outcome.</p></sec><sec id="s5"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s6"><title>Cite this paper</title><p>Popa, C., Mbaye, M., Thioub, M., Riem, T., Daumas-Duport, B., Asseray, N. and Robert, R. (2019) Acute Paraplegia Due to Salmonella brandenburg Spondylodiscitis: Case Report. Open Journal of Modern Neurosurgery, 9, 327-337. https://doi.org/10.4236/ojmn.2019.93031</p></sec></body><back><ref-list><title>References</title><ref id="scirp.93996-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Maiuri, F., Iaconetta, G., Gallicchio, B., Manto, A. and Briganti, F. (1997) Spondylodiscitis. Clinical and Magnetic Resonance Diagnosis. Spine, 22, 1741-1746.  
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