<?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">IJOHNS</journal-id><journal-title-group><journal-title>International Journal of Otolaryngology and Head &amp; Neck Surgery</journal-title></journal-title-group><issn pub-type="epub">2168-5452</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ijohns.2022.114020</article-id><article-id pub-id-type="publisher-id">IJOHNS-118805</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>
 
 
  Larynx Cancer: Review of 11 Years of Activity in the ENT and Head and Neck Surgery Department of University Hospital Gabriel Toure, Bamako
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Diarra</surname><given-names>Kassim</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>Konate</surname><given-names>Nfaly</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>Sanogo</surname><given-names>Harouna</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>Katile</surname><given-names>Oumar</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>Dembele</surname><given-names>Yaya</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>Soumaoro</surname><given-names>Siaka</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>Guindo</surname><given-names>Boubacary</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>Cisse</surname><given-names>Naoma</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>Coulibaly</surname><given-names>Kalifa</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>Kone</surname><given-names>Fatogoma Issa</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>Doumbia</surname><given-names>Kadidiatou</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>Keita</surname><given-names>Mohamed Amadou</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>ENT and Head and Neck Surgery Department, Reference Health Kalanbancoro, Bamako, Mali</addr-line></aff><aff id="aff1"><addr-line>ENT and Head and Neck Surgery Department, Gabriel Toure, Bamako, Mali</addr-line></aff><aff id="aff3"><addr-line>Army Polyclinic Kati, Bamako, Mali</addr-line></aff><pub-date pub-type="epub"><day>11</day><month>07</month><year>2022</year></pub-date><volume>11</volume><issue>04</issue><fpage>193</fpage><lpage>201</lpage><history><date date-type="received"><day>11,</day>	<month>May</month>	<year>2022</year></date><date date-type="rev-recd"><day>25,</day>	<month>July</month>	<year>2022</year>	</date><date date-type="accepted"><day>28,</day>	<month>July</month>	<year>2022</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>
 
 
  <b>Objectives:</b>
   To study the epidemio-clinical, therapeutic and evolutionary aspects of laryngeal cancers in the ENT department of the University Hospital Gabriel Toure.
   
  <b>Materials and Methods:</b>
   This was a descriptive, retrospective study over a period of 11 years from January 2008 to December 2019. We made an exhaustive sampling of all cases of malignant tumor
  s
   of the larynx in the ENT department of the University Hospital Gabriel TOURE. Variables studied: frequency, sex, age, clinic, imaging, histology, TNM classification, treatment received and follow-up time was 1 to 11 years.
   
  <b>Result:</b>
   we noted a male predominance (44 men/13 women). The average age was 52.23 years
  ,
   with extremes of 32 and 74 years. Smoking was reported by 40 patients (72% of cases). The average in pack
  -
  years is 29.32 with extremes of 4 to 60 packs/
   
  year. Alcoholism was reported by 6 patients (9% of cases). Squamous cell carcinoma was the predominant histological type (100%)
  ;
   extension to 2 or 3 floors was objectified in 69% of cases. Complementary radiotherapy in 26 patients after total laryngectomy. Chemotherapy was done in a neoadjuvant situation in 36 cases. Overall survival was: 52.6% at 1 year, 33.3% at 3 years; 26.3% at 5 years and 12.28% at 11 years. <b>Conclusion:</b> Most often
  ,
   late diagnosis 
  is 
  due to the absence of a national strategy and the underestimation of the first symptoms. Surgery coupled with radiotherapy is the treatment of choice.
 
</p></abstract><kwd-group><kwd>Laryngeal Cancer</kwd><kwd> Histology</kwd><kwd> Treatment</kwd><kwd> Follow-Up</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Laryngeal cancer represents 3.5% of malignant tumors diagnosed annually worldwide, causing 20,000 deaths corresponding to 1% of cancer deaths [<xref ref-type="bibr" rid="scirp.118805-ref1">1</xref>]. The number of new cases of laryngeal cancer in metropolitan France in 2018 is estimated at 3160, 87% of which were in men. World standardized incidence rates (TSM) are 4.8 cases per 100,000 person-years in men and 0.7 per 100,000 person-years in women (male/female ratio equal to 6.9) [<xref ref-type="bibr" rid="scirp.118805-ref2">2</xref>]. Its standardized net survival rate at 5 years: is 56% (56% in men and 59% in women) [<xref ref-type="bibr" rid="scirp.118805-ref3">3</xref>]. Medical imaging, in the particular scanner, MRI, PET, makes it possible to specify the site as well as the local and regional extension. [<xref ref-type="bibr" rid="scirp.118805-ref4">4</xref>]. squamous cell carcinoma is the most frequent histological type (95%) [<xref ref-type="bibr" rid="scirp.118805-ref4">4</xref>]. From 2008 to 2018 according to the Mali cancer registry report, laryngeal cancer was 1.3% in men, i.e., 7 cases per year and 0.5% in women, i.e., 4 cases per year of all cancers in Mali with an incidence of 0.8 per 100,000 inhabitants in men and 0.5 per 100,000 inhabitants in women [<xref ref-type="bibr" rid="scirp.118805-ref5">5</xref>]. Suppose laryngeal cancer is a ubiquitous pathology. There were no specific registers on this subject in the service. Thus the objective was to study the epidemio-clinical, therapeutic and evolutionary aspects of malignant laryngeal tumors in the ENT department of the University Hospital Gabriel Toure.</p></sec><sec id="s2"><title>2. Materials and Methods</title><p>This was a descriptive, retrospective study over a period of 11 years from January 2008 to December 2019. We made an exhaustive sampling of all cases of malignant tumors of the larynx in the ENT department of the University Hospital Gabriel Toure.</p><p>Inclusion criteria:</p><p>Records of patients, men and women of all ages seen and treated for laryngeal cancer in the ENT department of the Gabriel Toure hospital in Bamako.</p><p>Non-inclusion criteria:</p><p>Incomplete files, patients who have refused any therapeutic acts, any patient treated outside the said interval and who does not present any histological evidence.</p><p>Sampling: The sampling was exhaustive and we obtained 57 cases during the study period.</p><p>Variables studied:</p><p>Frequency, sex, age, socio-economic status, geographical origin, lifestyle (alcohol-tobacco intoxication), consultation time, signs, site of lesion, pharyngolaryngeal CT scan, Frontal chest X-ray, Abdominal ultrasound, macroscopic aspect of the lesion, pan endoscopy, histology, TNM classification, treatment received.</p><p>Follow-up time: it was 1 to 11 years.</p><p>Ethical and administrative considerations:</p><p>This is a purely scientific work that aims to improve the care of patients with laryngeal cancer. Anonymity was strictly respected. The results will be used to improve the quality of laryngeal cancer management. The consent of the patients or their relatives (accompanying) was obtained beforehand.</p></sec><sec id="s3"><title>3. Results</title><p>We collected 57 cases of laryngeal cancer over a period of 11 years and it represented 2.15% of ENT hospitalizations, i.e., an annual frequency of about 6 cases (<xref ref-type="table" rid="table1">Table 1</xref>). A clear male predominance was highlighted (44 men/13 women). The average age for all sexes combined was 52.23 years with extremes of 32 and 74 years (<xref ref-type="table" rid="table2">Table 2</xref>). Smoking was reported by 40 patients (72% of cases). The average in pack-years is 29.32 with extremes of 4 to 60 pack-years. Alcoholism was reported by 6 patients (9% of cases). In our series, 17 patients had a medical history (30%). Thus 4 of our patients had a history of treated pulmonary tuberculosis, 2 cases of type diabetes, two patients had GERD and 2 two patients were carriers of heart disease. The time between the start of the symptoms and the consultation was on average about 18.5 months with extremes ranging from 3 to 52 months, and 65% of our patients only consulted after a delay of 8 months and more. Dysphonia was the main symptom in 100% of cases, whether or not associated with dyspnea (89%), dysphagia (67%), and cervical lymphadenopathy (56%). There was an invasion of the three laryngeal stages at the time of diagnosis in 37% of cases. Glottic involvement in 4% of cases, glotto-supraglottic involvement in 32% of cases, and glotto-subglottic involvement in 28% of cases (<xref ref-type="table" rid="table3">Table 3</xref>).</p><p>The pharyngolaryngeal computed tomography was performed in all our patients and made it possible to better specify the extension towards the regions difficult to exploit by endoscopy, to classify the tumor and also to evaluate the</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Distribution of patients by year of recruitment</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Year of recruitment</th><th align="center" valign="middle" >Effective</th><th align="center" valign="middle" >Percentage</th></tr></thead><tr><td align="center" valign="middle" >2008</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >3.6</td></tr><tr><td align="center" valign="middle" >2009</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >1.8</td></tr><tr><td align="center" valign="middle" >2010</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >5.3</td></tr><tr><td align="center" valign="middle" >2011</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >5.3</td></tr><tr><td align="center" valign="middle" >2012</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >7.0</td></tr><tr><td align="center" valign="middle" >2013</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >7.0</td></tr><tr><td align="center" valign="middle" >2014</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >8.8</td></tr><tr><td align="center" valign="middle" >2015</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >7.0</td></tr><tr><td align="center" valign="middle" >2016</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >12.3</td></tr><tr><td align="center" valign="middle" >2017</td><td align="center" valign="middle" >9</td><td align="center" valign="middle" >15.8</td></tr><tr><td align="center" valign="middle" >2018</td><td align="center" valign="middle" >10</td><td align="center" valign="middle" >17.5</td></tr><tr><td align="center" valign="middle" >2019</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >8.8</td></tr><tr><td align="center" valign="middle" >total</td><td align="center" valign="middle" >57</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Distribution of patients by age group</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Age range</th><th align="center" valign="middle" >Effective</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >[30 - 40 years old]</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >3</td></tr><tr><td align="center" valign="middle" >[41- 50 years old]</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >11</td></tr><tr><td align="center" valign="middle" >[51- 60 years old]</td><td align="center" valign="middle" >27</td><td align="center" valign="middle" >47</td></tr><tr><td align="center" valign="middle" >[61 - 70 years old]</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >30</td></tr><tr><td align="center" valign="middle" >[71 years older]</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >9</td></tr><tr><td align="center" valign="middle" >TOTAL</td><td align="center" valign="middle" >57</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Distribution of patients according to tumor site</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Tumor location</th><th align="center" valign="middle" >Effective</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Glottic stage</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >4</td></tr><tr><td align="center" valign="middle" >Glotto-sus-glottic stage</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >32</td></tr><tr><td align="center" valign="middle" >Glotto-subglottic stage</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" >28</td></tr><tr><td align="center" valign="middle" >Larynx Totals</td><td align="center" valign="middle" >21</td><td align="center" valign="middle" >37</td></tr><tr><td align="center" valign="middle" >TOTAL</td><td align="center" valign="middle" >57</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><p>lymph node involvement, and was associated with the exploration of the thoracic floor in almost all patients. It found an invasion of the HTE lodge in 9 patients, the paralaryngeal fatty spaces in 17 patients, the piriform sinus in 8 patients, and the aryepiglottic folds were affected in 15 patients. Squamous cell carcinoma is the predominant histological type (100%), and extension to 2 or 3 floors was objectified in 69% of cases. Regarding lymph node extension, we noted a single ipsilateral lymph node less than or equal to 3 cm (N1) in 44% of cases and a single ipsilateral lymph node involvement between 3 and 6 cm (N2a) in 10% of cases. 14% of patients had multiple ipsilateral lymph node metastases all less than or equal to 6 cm (stage N2b), and 11% of patients had bilateral or contralateral lymph node metastases less than or equal to 6 cm (stage N2c). Lymph node involvement greater than 6 cm (N3) was found in only 5% of cases. At the end of the TNM classification, 53% of our patients, i.e., 30 cases, had stage IV cancer, 2 cases of stage I cancer, i.e., 3% of cases, 8 cases of stage II cancer, i.e., 14% of cases and 17 cases of cancer, stage III, i.e., 30% of cases (<xref ref-type="table" rid="table4">Table 4</xref>). In our series, 26 patients underwent surgical treatment (46% of cases). Total laryngectomy associated with lymph node dissection was the only procedure performed for all patients treated surgically. Of which one (1) with associated thyroidectomy saw the invasion of the thyroid lobes and were referred for additional radiotherapy. Of all the patients treated with radiotherapy, whether in an adjuvant or exclusive external situation: 62% (either 23 cases) received a radio-chemotherapy combination with weekly cisplatin at a dose of 40 mg/m<sup>2</sup>. It should be noted that 48% received radiotherapy alone. The most widely used radiotherapy protocol (in all patients) is as follows: 70 Gy/total dose: at a dose of</p><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Distribution of patients according to stage T</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Location</th><th align="center" valign="middle" >Effective</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Stage T1</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >3</td></tr><tr><td align="center" valign="middle" >Stage T2</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >14</td></tr><tr><td align="center" valign="middle" >Stage T3</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >30</td></tr><tr><td align="center" valign="middle" >Stage T4</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >53</td></tr></tbody></table></table-wrap><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Distribution of patients according to overall survival rate after treatment</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Overall survival</th><th align="center" valign="middle" >Effectives</th><th align="center" valign="middle" >Percentage</th></tr></thead><tr><td align="center" valign="middle" >At 1 year</td><td align="center" valign="middle" >30</td><td align="center" valign="middle" >52.6</td></tr><tr><td align="center" valign="middle" >At 3 years old</td><td align="center" valign="middle" >19</td><td align="center" valign="middle" >33.3</td></tr><tr><td align="center" valign="middle" >At 5 years old</td><td align="center" valign="middle" >15</td><td align="center" valign="middle" >26.3</td></tr><tr><td align="center" valign="middle" >At 11 years old</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >12.2</td></tr></tbody></table></table-wrap><p>70 Gy due to 5 sessions of 2 Gy per fraction per week. Chemotherapy was done in a neoadjuvant situation in 36 cases and the chemotherapy protocol that was most used in 32 cases was carboplatin and CDDP paclitaxel 300 mg every 21 days. Concomitant chemotherapy was performed in 23 cases, with weekly cisplatin in all cases. Palliative chemotherapy was performed in two (2) metastatic patients based on 5fluorouracil-cisplatin.</p><p>At the end of the treatments received by our patients and after follow-up, we noted 7 cases of local recurrence, 3 cases of lymph node recurrence, 1 case of metastatic recurrence (pulmonary metastasis. In our series, the overall survival of the disease was 26.31% at 5 years (<xref ref-type="table" rid="table5">Table 5</xref>).</p></sec><sec id="s4"><title>4. Discussion and Comment</title><sec id="s4_1"><title>4.1. Methodological Aspect</title><p>Our study, which focused on the retrospective analysis of hospitalization records, was confronted with certain number of difficulties:</p><p>- Inaccessibility of patients to imaging and to certain biological analyses, the repetition of which was part of the therapeutic follow-up of patients.</p><p>- Poor archiving of files.</p><p>- The loading of contact of certain patients.</p></sec><sec id="s4_2"><title>4.2. Hospital Frequency Aspect</title><p>We collected 57 cases of laryngeal cancer over a period of 11 years and it represented 2.15% of ENT hospitalizations, i.e., an annual frequency of about 6 cases. In our series, the incidence of laryngeal cancer was 0.8 per 100,000 inhabitants in men and 0.5 per 100,000 inhabitants in women. Our results are lower than those of Miss Mohssin Asmae [<xref ref-type="bibr" rid="scirp.118805-ref6">6</xref>], who found 2.4 per 100,000 inhabitants for men and 0.4 per 100,000 inhabitants for women according to the Grand Casablanca cancer registry and according to Cl&#233;ment Gauche [<xref ref-type="bibr" rid="scirp.118805-ref7">7</xref>] in France, the incidence was 2.5 per 100,000 inhabitants in men and 0.2 in women. This could be explained by the difficulties of access to care in our context, and the growing increase in industrial settings in developed countries, but tobacco and alcohol remain clear contributing factors [<xref ref-type="bibr" rid="scirp.118805-ref4">4</xref>].</p></sec><sec id="s4_3"><title>4.3. Age</title><p>The predilection age for laryngeal cancer is between 45 and 70 years old with a clear predominance between the fifth and sixth decades of life, whereas it is uncommon before 45 and after 70 years [<xref ref-type="bibr" rid="scirp.118805-ref8">8</xref>], but we observe a recrudescence of cancer in younger and younger subjects in connection with the precocity of alcohol and tobacco intoxication, as is the case in our series. The average age varies according to the series but remains between 55 and 65 years old. In our study, the average age was 52 with extremes ranging from 32 to 74, which agrees with the results found in the series but remains relatively younger [<xref ref-type="bibr" rid="scirp.118805-ref8">8</xref>].</p></sec><sec id="s4_4"><title>4.4. Risk Factors</title><p>In our study, forty of our patients are chronic smokers, i.e., 70%. In the other non-smoking patients, the notion of passive smoking was clarified in two of our patients. Indeed, the risk is 2 to 12 times higher in smokers compared to non-smokers [<xref ref-type="bibr" rid="scirp.118805-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.118805-ref10">10</xref>]. Thus, Mrs. Madrare Lamyae [<xref ref-type="bibr" rid="scirp.118805-ref11">11</xref>] found that 85.3% of smokers in a series of 34 cancer cases with an average consumption of 10 to 50 packets per year. Sadek Houda [<xref ref-type="bibr" rid="scirp.118805-ref12">12</xref>] highlighted in his series of 100 cases, 86 chronic smokers, (86%), with an average consumption exceeding 4 to 100 packets per year. The alcohol-tobacco association was found in 10 of our patients, 5 patients consumed it occasionally. In our series, 17.53% consumed alcohol frequently or occasionally. Determining the quantity in our context is difficult. Indeed, when we push the questioning with the patients about their toxic habits, they generally tend to deny their alcoholic habits, unlike smoking, which explains the low percentage of alcoholism in our study.</p></sec><sec id="s4_5"><title>4.5. Clinical Aspect</title><p>The consultation period is generally short in developed countries compared to Third World countries or the period can be spread over several years, as follows: we observed in our series an average period of 8.54 months with extremes ranging from 3 to 52 months. Our results are consistent with those of the literature [<xref ref-type="bibr" rid="scirp.118805-ref13">13</xref>], whose average consultation time was 8 months with extremes ranging from one month to 24 months. Several reasons could explain this late delay: The trivialization of certain symptoms (dysphonia, dysphagia) despite their persistence, the absence of initial pain and the difficulty of access to care. The delay in consultation can also be attributed to the first recourse to traditional medicine and the distance from specialized services. Finally, there is the diagnostic delay, which represents the time between the consultation of an ENT specialist and the histological establishment of the diagnosis, as well as the delay in the initiation of treatment. This delay is very long, allowing the evolution and the extension of the tumoral lesions.</p><p>The clinical signs evoking laryngeal cancer are classically dysphonia, dysphagia and dyspnea. The clinical signs already mentioned can be supplemented by a dry, irritating but persistent cough, a sensation of a foreign body, reflex otalgia on the side of the tumor lesion, which was found in only one of our patients, more rarely, hemoptoic sputum attracts attention and will lead to consultation [<xref ref-type="bibr" rid="scirp.118805-ref1">1</xref>]. Thus the data on symptoms in national and international series, thus showing a good correlation with the data of our series.</p></sec><sec id="s4_6"><title>4.6. Imaging Aspect</title><p>Imaging mainly provides additional information to endoscopy on deep extension. In our series, chest X-ray, abdominal ultrasound and cervico-thoracic CT were systematically used as staging assessments; but CT plays a key role in monitoring treated patients, detecting possible complications of treatment and looking for signs of recurrence (appearance of a mass, thickening of lymphadenopathy, etc.). In the literature [<xref ref-type="bibr" rid="scirp.118805-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.118805-ref8">8</xref>] in addition to the examinations aroused cervical MRI and PET-scan seem to be more specific and more sensitive to the search for metastasis. These extension assessments are not available from us, but cervico-thoracic CT remains the most useful examination to complete the extension assessment in all series.</p></sec><sec id="s4_7"><title>4.7. Histological Appearance</title><p>Squamous cell carcinoma represents the dominant histological form of malignant tumors of the larynx. This is found in all the series reported in the literature. Diakit&#233; [<xref ref-type="bibr" rid="scirp.118805-ref13">13</xref>] in his series of 404 patients, found only one case of adenoid cystic carcinoma; squamous cell carcinoma was found in all the other patients. In our series, squamous cell carcinoma was found in 100% of cases, which agrees with most of the results reported in the literature. The well to moderately differentiated form represented 96%, and the poorly differentiated aspect constituted 4%.</p></sec><sec id="s4_8"><title>4.8. Therapeutic Aspects</title><p>Three methods are available: surgery externally or by endoscopy, radiotherapy and chemotherapy. Total laryngectomy (TL) is indicated when the local extension of the primary tumor contraindicates the performance of a functional partial laryngectomy. Indicated for laryngeal carcinomas with cartilaginous and/or subglottic extension with involvement of the cricoid [<xref ref-type="bibr" rid="scirp.118805-ref1">1</xref>]. In our study, we used LT in 26 patients (46%). The performance of partial surgery stems from the wish of some patients who consent to the resection of part of their larynx, provided that swallowing, breathing and phonation are safeguarded [<xref ref-type="bibr" rid="scirp.118805-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.118805-ref14">14</xref>]. We did not have recourse since all our patients consulted at a late stage of the disease. The initial lymph node status of patients with squamous cell carcinoma of the upper aerodigestive tract is a factor influencing the prognosis. Patients without lymph node involvement have a favorable prognosis, whereas metastatic lymph node dissemination clearly reduces survival. In our series, 84% of patients had cervical lymph node metastases at the time of diagnosis. After a total laryngectomy, radiotherapy is delivered by two opposite and parallel fields on the tumor excision area and the cervical lymph node areas.</p><p>It takes into account the histopathological criteria of the surgical specimen: analysis of resections of the tumor resection area, number of metastatic adenopathies and their capsular rupture, carcinomatous lymphangitis and emboli [<xref ref-type="bibr" rid="scirp.118805-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.118805-ref14">14</xref>]. In our work, radiotherapy was performed in 37 patients (65% of cases): adjuvant radiotherapy in 12 cases, and exclusive external radiotherapy in 25 cases. Of all the patients treated with radiotherapy, 62% (23 cases) received a combination radio-chemotherapy with weekly cisplatin at a dose of 40 mg/m<sup>2</sup> and 48% received radiotherapy alone.</p><p>Chemotherapy: Considered for a long time as a treatment for recurrent and/or metastatic tumors, it made a strong entry into curative treatments with the appearance, at the end of the 1970s, of platinum salts and their association with 5-fluorouracil. In ENT oncology, systemic treatment now has a validated place in the therapeutic arsenal. Use in induction prior to locoregional treatments with the objective of organ preservation. It was done in 48 patients in our study (84.21%).</p></sec><sec id="s4_9"><title>4.9. Prognostic Aspect</title><p>In the literature, the overall survival rate (all sexes combined) at 5 years varies between 66 and 87% [<xref ref-type="bibr" rid="scirp.118805-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.118805-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.118805-ref14">14</xref>] depending on the tumor location, the therapeutic approach, the stage T, N and M and associated comorbidities. The overall prognosis is the best of that of the various tumors of the upper aerodigestive tract [<xref ref-type="bibr" rid="scirp.118805-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.118805-ref14">14</xref>]. In our series, the 5-year survival was 26.3%; this result is significantly lower than those of the international series. This low rate could be explained not only by the delay in diagnosis but also by the difficult access to postoperative radio-chemotherapy.</p></sec></sec><sec id="s5"><title>5. Conclusions</title><p>Laryngeal cancer is a heavy pathology, whether by its repercussions or by its management. The absence of a national strategy concerning this pathology and the underestimation of the first symptoms very often lead to the diagnosis being made at a late stage, which explains the absence of superficial cancers in our series. This same diagnostic delay is also weighed down by a long therapeutic delay due to the large influx of patients to the only radiotherapy and medical oncology department in the country.</p><p>The prognosis of laryngeal cancer remains lower in our series compared to international data. Finally, the fight against alcohol and tobacco intoxication remains the best way to reduce its incidence.</p></sec><sec id="s6"><title>Conflicts of Interest</title><p>The authors declare no conflict of interest.</p></sec><sec id="s7"><title>Cite this paper</title><p>Kassim, D., Nfaly, K., Harouna, S., Oumar, K., Yaya, D., Siaka, S., Boubacary, G., Naoma, C., Kalifa, C., Issa, K.F., Kadidiatou, D. and Amadou, K.M. (2022) Larynx Cancer: Review of 11 Years of Activity in the ENT and Head and Neck Surgery Department of University Hospital Gabriel Toure, Bamako. International Journal of Otolaryngology and Head &amp; Neck Surgery, 11, 193-201. https://doi.org/10.4236/ijohns.2022.114020</p></sec></body><back><ref-list><title>References</title><ref id="scirp.118805-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Prades, J.-M. and Reyt, E. (2013) Cancers du larynx. EMC-Oto-Rhino-Laryngologie, 8, 1-15.</mixed-citation></ref><ref id="scirp.118805-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Defossez, G., Le Guyader-Peyrou, S. and Uhry, Z., et al. (2019) Estimations nationales de l’incidence et de la mortalité par cancer en France métropolitaine entre 1990 et 2018. Santé publique France, Saint-Maurice.</mixed-citation></ref><ref id="scirp.118805-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Institut national du cancer (2018) Les cancers en France, édition 2017. Institut national du cancer, Boulogne-Billancourt.</mixed-citation></ref><ref id="scirp.118805-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Daniel, B., Denis, A., Stephane, H., Dana, H. and Jean Francois, P. (2008) Traité d’ORL. In Jean L, Sophie P. Cancer de larynx et l’hyopharynx. Médecine science Flammarion, Paris, 588-595.</mixed-citation></ref><ref id="scirp.118805-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Service d’anatomie cytologie pathologie (2018) rapport des registres des cancers au Mali. registre des cancers du Mali.</mixed-citation></ref><ref id="scirp.118805-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Asmae, M. (2019) Laryngectomie totale: Expérience du service d’ORL du CHU Hassan II de Fès à propos de 32 cas. Faculte de Medecine et de Pharmacie de Fès, Sidi Harazem Fès.</mixed-citation></ref><ref id="scirp.118805-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Gauche, C. (2016) Prise en charge ganglionnaire des cancers du larynx classé T1-T2N0, à propos de 384 cas. Faculté de médecine Toulouse-III-Paul-Sabatier, Toulouse.</mixed-citation></ref><ref id="scirp.118805-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Lefebvre, J.-L. and Chevalier, D. (2005) Cancers du larynx. EMC-Oto-Rhino-Lary ngologie, 2, 432-457. https://doi.org/10.1016/j.emcorl.2005.09.005</mixed-citation></ref><ref id="scirp.118805-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Gallus, S., Bosetti, C., Franceschi, S. and Levi, F. (2003) Laryngeal Cancer in Women: Tobacco, Alcohol, Nutritional and Hormonal Factors. Cancer Epidemiol Biomarkers Prevention, 12, 514-517.</mixed-citation></ref><ref id="scirp.118805-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Talamini, R., et al. (2012) Combined Effect of Tobacco and Alcohol on Laryngeal Cancer Risk: A Case-Control Study. Cancer Causes Control, 13, 957-964.https://doi.org/10.1023/A:1021944123914</mixed-citation></ref><ref id="scirp.118805-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Lamyae, M. (2011) Le cancer du larynx (A propos de 34 cas). Faculté de médecine et de pharmacie de Fès, Sidi Harazem Fès.</mixed-citation></ref><ref id="scirp.118805-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Sadek, H. (2010) Profils épidémiologique, clinique, thérapeutique et évolutif du cancer de larynx au service d’oncologie du CHU Mohamed VI entre 2003 et 2008 à propos de 34 cas. Faculté de médecine et de pharmacie de Fès, Sidi Harazem Fès.</mixed-citation></ref><ref id="scirp.118805-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Diakité, A. (2005) Cancer du larynx: Expérience de l’institut national d’oncologie de Rabat, à propos de 404 cas. Cancer/Radiothérapie, 16, 545. https://doi.org/10.1016/j.canrad.2012.07.085</mixed-citation></ref><ref id="scirp.118805-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Obid, R. Redlich, M. and Tomeh, C. (2019) Tomeh, The Treatment of Laryngeal Cancer. Oral and Maxillofacial Surgery Clinics of North America, 31, 1 11.https://doi.org/10.1016/j.coms.2018.09.001</mixed-citation></ref></ref-list></back></article>