<?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">SS</journal-id><journal-title-group><journal-title>Surgical Science</journal-title></journal-title-group><issn pub-type="epub">2157-9407</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ss.2018.98031</article-id><article-id pub-id-type="publisher-id">SS-86787</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>
 
 
  Management of Spinal Schwannomas in Gabriel Tour&#233; Hospital: Review of 11 Cases
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Youssouf</surname><given-names>Sogoba</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Boubacar</surname><given-names>Sogoba</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>Drissa</surname><given-names>Kanikomo</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>Seybou</surname><given-names>Hassane Diallo</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>Djenè</surname><given-names>Kourouma</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>Oumar</surname><given-names>Coulibaly</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>Issa</surname><given-names>Amadou</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>Moustapha</surname><given-names>Mangané</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>Hamidou</surname><given-names>Almeimoune</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>Madani</surname><given-names>Thierno Diop</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>Youssoufa</surname><given-names>Maiga</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>Broulaye</surname><given-names>Samaké</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>Djibo</surname><given-names>M. Diango</given-names></name><xref ref-type="aff" rid="aff5"><sup>5</sup></xref></contrib></contrib-group><aff id="aff5"><addr-line>Department of Anesthesiology and ICU, H&amp;amp;#244;pital Gabriel Touré, Bamako, Mali</addr-line></aff><aff id="aff4"><addr-line>Department of Pediatric Surgery, H&amp;amp;#244;pital Gabriel Touré, Bamako, Mali</addr-line></aff><aff id="aff3"><addr-line>Department of Neurosurgery, H&amp;amp;#244;pital du Mali, Bamako, Mali</addr-line></aff><aff id="aff2"><addr-line>Department of Neurology, H&amp;amp;#244;pital Gabriel Touré, Bamako, Mali</addr-line></aff><aff id="aff1"><addr-line>Department of Neurosurgery, H&amp;amp;#244;pital Gabriel Touré, Bamako, Mali</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>sogobayoussouf@yahoo.fr(YS)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>13</day><month>08</month><year>2018</year></pub-date><volume>09</volume><issue>08</issue><fpage>256</fpage><lpage>261</lpage><history><date date-type="received"><day>27,</day>	<month>July</month>	<year>2018</year></date><date date-type="rev-recd"><day>19,</day>	<month>August</month>	<year>2018</year>	</date><date date-type="accepted"><day>22,</day>	<month>August</month>	<year>2018</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>
 
 
  Background: Spinal schwannomas are common tumors of spinal neoplasm and account for about 25% of intradural spinal cord tumors in adults. They are generally benign and slow-growing. Advanced in radiologic and surgical techniques have brought about better surgical results. The goal of surgical treatment must be total resection if possible. In this report, the authors present the incidence, clinical presentation, localization, and results of surgically treated spinal schwannomas. The results of a literature review are also presented. 
  Methods: Eleven consecutive patients with histologically confirmed spinal schwannomas were treated from January 2013 to December 2016 in the neurosurgical department of Gabriel Tour&#233; Hospital, Bamako, Mali. Neuroradiological diagnosis was made, CT scan in 7 patients, and MRI in 4 patients. All patients were operated on via the posterior approach. All cases were surgically excised, and they were confirmed to be schwannomas by pathologists. The patients were followed for 6 to 38 months (mean 28 months). Functional outcome was assessed using the motor grade and sensory change. 
  Results: There were 11 patients with 7 (63.6%) males and 4 (36.4%) females. The mean age was 40.3 years (range 23 - 62 years). The most common symptom at the time of diagnosis was radicular pain in 9 (81.8%) patients followed by motor weakness in 8 (72.7%) patients. The most frequent site of spinal schwannomas was the thoracic region in 5 (45.5%) patients. During surgery, Gross-total resec-tion was achieved in 8 patients (72.7%) and subtotal removal in 3 (27.3%) patients. Histological findings were benign schwannoma in all cases. Postoperative complications developed in two patients, including one with cerebrospinal fluid leakage and other one with wound infection. In the short-term follow-up period, most of the patients (90.9%) appeared to be improved in comparison with their preoperative neurological status. There was no operative mortality. 
  Conclusion: In this study, the clinical manifestations and surgical results of 11 cases of spinal schwannoma have been reviewed. Early diagnosis and appropriate treatment are essential for good outcome.
 
</p></abstract><kwd-group><kwd>Spinal Schwannoma</kwd><kwd> Spine Surgery</kwd><kwd> Recurrence</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Intraspinal tumors are common neurogenic tumors, accounting for approximately 15% of central nervous system tumors [<xref ref-type="bibr" rid="scirp.86787-ref1">1</xref>]. Spinal schwannomas account for about 25% of intradural spinal cord tumors in adults [<xref ref-type="bibr" rid="scirp.86787-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref5">5</xref>]. The incidence of spinal schwannomas varies between 0.3 - 0.4 cases/100,000 persons per year [<xref ref-type="bibr" rid="scirp.86787-ref5">5</xref>]. It is common benign tumor in spinal canal [<xref ref-type="bibr" rid="scirp.86787-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref7">7</xref>] and due to the slow tumor growth, hidden onset and no specific symptoms and signs, its early diagnosis is more difficult, and some patients are not treated until they are paralyzed. The total excision of the lesion, which is the generally reachable goal of surgery, allows for good results in the cases in which the preoperative clinical findings are not particularly severe. In this study, the authors report 11 cases of spinal schwannomas who were admitted to the Gabriel Tour&#233; Hospital from January 2013 to December 2016. The aim of this study was to analyze clinical characteristics and outcome after surgical treatment of patients with spinal schwannomas.</p></sec><sec id="s2"><title>2. Methods</title><p>Eleven consecutive patients with histologically confirmed spinal schwannomas were treated from January 2013 to December 2016 in the neurosurgical department of Gabriel Tour&#233; Hospital, Bamako, Mali. Neuroradiological diagnosis was made, CT scan in 7 patients (<xref ref-type="fig" rid="fig1">Figure 1</xref>), and MRI in 4 patients (<xref ref-type="fig" rid="fig2">Figure 2</xref>). All patients were operated on via the posterior approach. All cases were surgically excised, and they were confirmed to be schwannomas by pathologists. The patients were followed for 6 to 38 months (mean 28 months). Functional outcome was assessed using the motor grade and sensory change.</p></sec><sec id="s3"><title>3. Results</title><p>There were 11 patients with 7 (63.6%) males and 4 (36.4%) females. The mean age was 40.3 years (range 23 - 62 years). The courses of disease ranged from 10 to 68 months (mean 28 months). The most common symptom at the time of</p><p>diagnosis was radicular pain in 9 (81.8%) patients followed by motor weakness in 8 (72.7%) patients (<xref ref-type="table" rid="table1">Table 1</xref>). The most frequent site of spinal schwannomas was the thoracic region in 5 (45.5%) patients. Three (27.3%) cases were located in cervical area, and other 3 (27.5%) in lumbar region. All of the tumors were removed surgically via laminectomy through posterior approach. Gross-total resection was achieved in 8 (72.7%) patients (<xref ref-type="fig" rid="fig1">Figure 1</xref> and <xref ref-type="fig" rid="fig2">Figure 2</xref>) and subtotal removal in 3 (27.3%) patients. Histological findings were benign schwannoma in all cases. The patients were followed for 6 to 38 months (mean 28 months). In the follow-up period, most of the patients (90.9%) appeared to be improved in comparison with their preoperative neurological status (<xref ref-type="table" rid="table2">Table 2</xref>). There was no operative complication or mortality and no recurrence in the short-term follow-up.</p></sec><sec id="s4"><title>4. Discussion</title><p>Spinal schwannomas are slow-growing benign tumors with a capsule that originates in the myelin sheath. They account for about 25% of primary intradural spinal cord tumors in adults. Several authors had reported that there is equal incidence in males and females [<xref ref-type="bibr" rid="scirp.86787-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref8">8</xref>]. In our study, the prevalence was higher in males with 63.6%. The incidence of spinal schwannoma varies with the</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Clinical Characteristics of spinal schwannoma in 11 patients</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Symptoms</th><th align="center" valign="middle" >N (%)</th></tr></thead><tr><td align="center" valign="middle" >Radicular pain</td><td align="center" valign="middle" >9 (81.8)</td></tr><tr><td align="center" valign="middle" >Motor weakness</td><td align="center" valign="middle" >8 (72.7)</td></tr><tr><td align="center" valign="middle" >Sensory loss</td><td align="center" valign="middle" >5 (45.4)</td></tr><tr><td align="center" valign="middle" >Back pain</td><td align="center" valign="middle" >5 (45.4)</td></tr><tr><td align="center" valign="middle" >Sphincter disturbances</td><td align="center" valign="middle" >2 (18.2)</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Post-operative outcome of spinal schwannoma in 11 patients</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Outcome</th><th align="center" valign="middle" >N (%)</th></tr></thead><tr><td align="center" valign="middle" >Recovered</td><td align="center" valign="middle" >4 (36.4)</td></tr><tr><td align="center" valign="middle" >Improved</td><td align="center" valign="middle" >6 (54.5)</td></tr><tr><td align="center" valign="middle" >Stable</td><td align="center" valign="middle" >1 (9.1)</td></tr><tr><td align="center" valign="middle" >Worsened</td><td align="center" valign="middle" >0 (0)</td></tr><tr><td align="center" valign="middle" >Dead</td><td align="center" valign="middle" >0 (0)</td></tr></tbody></table></table-wrap><p>age of affected patients who are between the 4th and the 5th decade [<xref ref-type="bibr" rid="scirp.86787-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref9">9</xref>]. The mean age was 40.3 years in this report. The initial symptoms are varied in accordance with the level of the tumor. The main symptoms and signs are pain, paresthesia and sphincter disturbances. At the beginning the root pain is attributed to the disturbance of nerve conductivity because of the direct or indirect irritation of nerve root or root compression by the tumor [<xref ref-type="bibr" rid="scirp.86787-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref10">10</xref>]. Motor weakness occurs when compression increases to spinal cord, spinal tracts get damaged and myelopathy develops [<xref ref-type="bibr" rid="scirp.86787-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref12">12</xref>]. Our study confirms that pain is the most common presenting symptom in patients with spinal schwannomas [<xref ref-type="bibr" rid="scirp.86787-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref13">13</xref>]. Early diagnosis is critical because the long-term spinal cord compression may lead to permanent loss of function. The course of disease in this study was 10 - 68 months (mean 28 months) leading to weakness in 8 (72.7%) patients. Sphincter disturbances were found in 2 (18.2%) patients in our study while some authors have reported a rate of 5% [<xref ref-type="bibr" rid="scirp.86787-ref10">10</xref>]. Spinal schwannomas can occur at any level of the spinal column [<xref ref-type="bibr" rid="scirp.86787-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref14">14</xref>].</p><p>There is some discrepancy in the literature regarding the occurrence of spinal schwannomas along the longitudinal axis of the spine [<xref ref-type="bibr" rid="scirp.86787-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref13">13</xref>]. These inconsistencies may reflect ethnic differences in the incidence of schwannomas [<xref ref-type="bibr" rid="scirp.86787-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref14">14</xref>]. In our study, the higher incidence was seen in the thoracic region in 5 (45.5%) patients. In the literature, 70% to 80% of spinal schwannomas are reported to be intradural in location [<xref ref-type="bibr" rid="scirp.86787-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref15">15</xref>]. Our study also confirms that fact. There was no extradural-intradural, extradural or intramedullary schwannomas in our study. The goal of the surgical treatment in patients with spinal schwannomas is total tumor resection while preserving associated neurovascular structures and preventing neurological deterioration. There may be two obstacles to total resection: one is adhesion to the spinal cord; the other is critical structures attached to extradural components outside the spinal canal in the cervical region, such as the vertebral artery. In our study Gross-total resection was achieved in 8 (72.7%) patients. The authors of several studies have shown that schwannoma is associated with a higher rate of tumor recurrence [<xref ref-type="bibr" rid="scirp.86787-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref13">13</xref>]. There was no recurrence in this study. However, the relatively short followup period may explain these findings, because spinal schwannomas can recur many years after their initial resection. Klekamp J and Samii M [<xref ref-type="bibr" rid="scirp.86787-ref9">9</xref>] found that the recurrence rate was 10.7% after 5 years and 28.2% after 10 and 15 years. In our study, none of these patients required postoperative fixation. Postoperative instability can occur after resection removal of facet joints and require surgical stabilization [<xref ref-type="bibr" rid="scirp.86787-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref17">17</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref18">18</xref>]. One patient suffered from cerebrospinal fluid leakage after operation. The outcome of spinal schwannoma correlates to preoperative neurological condition of patient [<xref ref-type="bibr" rid="scirp.86787-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.86787-ref19">19</xref>]. In the follow-up period, most of our patients (90.9%) appeared to be improved in comparison with their preoperative neurological status.</p></sec><sec id="s5"><title>5. Conclusion</title><p>In this study, the clinical manifestations and surgical results of 11 cases of spinal schwannoma have been reviewed. Early diagnosis and appropriate treatment are essential for good outcome.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s7"><title>Cite this paper</title><p>Sogoba, Y., Sogoba, B., Kanikomo, D., Diallo, S.H., Kourouma, D., Coulibaly, O., Amadou, I., Mangan&#233;, M., Almeimoune, H., Diop, M.T., Maiga, Y., Samak&#233;, B. and Diango, D.M. (2018) Management of Spinal Schwannomas in Gabriel Tour&#233; Hospital: Review of 11 Cases. Surgical Science, 9, 256-261. https://doi.org/10.4236/ss.2018.98031</p></sec></body><back><ref-list><title>References</title><ref id="scirp.86787-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Weber, C., Gulati, S., Jakola, A.S., Habiba, S., Nygaard, &amp;#216;.P., Johannesen, T.B. and Solheim, O. 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