<?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">OJU</journal-id><journal-title-group><journal-title>Open Journal of Urology</journal-title></journal-title-group><issn pub-type="epub">2160-5440</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/oju.2020.106021</article-id><article-id pub-id-type="publisher-id">OJU-100159</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>
 
 
  Gangrene of the External Genitalia at the Regional University Hospital Center of Ouahigouya: Epidemiological Profile and Therapeutic Aspects
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Tiéoulé</surname><given-names>Mamadou Traore</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>Cl&amp;#244;taire</surname><given-names>Alexis Marie Kiemdiba Donega Yameogo</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>Moussa</surname><given-names>Kabore</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>Souleymane</surname><given-names>Ouedraogo</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Service d’urologie du CHU Yalgado Ouédraogo Ouagadougou, Ouaga, Ouagadougou, Burkina Faso</addr-line></aff><aff id="aff1"><addr-line>Service de chirurgie du CHU régional de Ouahigouya, Ouahigouya, Burkina Faso</addr-line></aff><pub-date pub-type="epub"><day>12</day><month>05</month><year>2020</year></pub-date><volume>10</volume><issue>06</issue><fpage>184</fpage><lpage>191</lpage><history><date date-type="received"><day>6,</day>	<month>March</month>	<year>2020</year></date><date date-type="rev-recd"><day>10,</day>	<month>May</month>	<year>2020</year>	</date><date date-type="accepted"><day>13,</day>	<month>May</month>	<year>2020</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>
 
 
  Introduction: Gangrene of extern genitary organs is a rapidly progressive necrotizing fasciitis of the perineum and external genitalia that results from a polymicrobial infection. Mortality remains high despite advances in resuscitation. We report the experience of the surgery department of the Regional University Hospital Center (CHUR) of Ouahigouya in order to describe the epidemiological profile and the therapeutic aspects of GOGE. 
  Patients and 
  methods: We carried out a descriptive and analytical retrospective study collecting 41 cases of Fournier’s gangrene treated over 63 months (from March 2013 to July 2018) in the surgical department of the Ouahigouya regional university hospital center. Ethical clearance was taken from the institutional ethics committee. 
  Results: The mean age of the patients was 65.02 &#177; 17.92 years with extremes of 23 years and 95 years. All patients were male. Urologic causes were the most common with 36.58% of cases. The average consultation time was 15.44 &#177; 16.04 days with extremes of 1 day and 60 days. All patients received resuscitation, bi or triantibiotherapy and surgical debridement. The mortality rate was 24.39%. The mean duration of hospitalization was 10.83 &#177; 6.257 days with extremes of 1 day and 60 days. 
  Conclusion: The Fournier’s gangrene always has a very high lethality. Improving the prognosis requires fast and effective management.
 
</p></abstract><kwd-group><kwd>Fournier’s Gangrene</kwd><kwd> Epidemiology</kwd><kwd> Emergency</kwd><kwd> Mortality</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Fournier external genitalia gangrene (GOGE) is a rapidly progressive necrotizing fasciitis of the perineum and external genitalia that results from polymicrobial infection [<xref ref-type="bibr" rid="scirp.100159-ref1">1</xref>]. In 1883 a French dermatologist named Jean Alfred Fournier reported five cases of gangrene of the external genitalia with no apparent cause in young men. This disease was called gangrene of Fournier [<xref ref-type="bibr" rid="scirp.100159-ref2">2</xref>]. The source of the infection can be urological, proctological or dermatological. However, in about 5% of cases GOGE is said to be idiopathic [<xref ref-type="bibr" rid="scirp.100159-ref1">1</xref>]. It is a rare urological emergency that can quickly put life threatening into play. Mortality remains high despite progress in resuscitation. It is estimated between 16% and 40% [<xref ref-type="bibr" rid="scirp.100159-ref3">3</xref>]. Management must be rapid and effective [<xref ref-type="bibr" rid="scirp.100159-ref4">4</xref>]. We report the experience of the surgery department of the Regional University Hospital Center (CHUR) of Ouahigouya in order to describe the epidemiological profile and the therapeutic aspects of GOGE.</p></sec><sec id="s2"><title>2. Patients and Method</title><p>This was a descriptive and analytical retrospective study of 41 patients treated over a period of 63 months (from March 2013 to July 2018) in the surgical department of CHUR Ouahigouya in Burkina Faso. Data were collected from hospital records and patient records. Epidemiological (age, sex, profession), diagnostic (time to consult, clinical examination on admission, biology), therapeutic (resuscitation, antibiotic therapy, debridement) and evolutionary (duration of hospitalization, survival) were studied. The statistical analysis was performed by the Statistical Package for the Social Sciences (SPSS) software in version 21.0. The tests used were Student’s t test and Fisher’s exact test. P &lt; 0.05 was considered statistically significant. The figures and tables were produced using Excel 2013 software. The confidentiality of the data was respected.</p></sec><sec id="s3"><title>3. Results</title><p>During the study period, we collected 41 cases of GOGE, an average of 7.8 cases per year. GOGE accounted for 0.54% (41/7617) of all admissions during the study period. The mean age of the patients was 65.02 &#177; 17.92 years with extremes of 23 and 95 years. <xref ref-type="fig" rid="fig1">Figure 1</xref> shows the distribution of patients by age group. All of the patients were male. Cultivators represented 85.36% (35/41) of the patients.</p><p><xref ref-type="table" rid="table1">Table 1</xref> gives the distribution of patients according to the favorable factors. Urological causes were the most frequent with 36.58% of cases.</p><p><xref ref-type="table" rid="table2">Table 2</xref> gives the distribution of patients according to etiologies.</p><p>The mean consultation time was 15.44 &#177; 16.04 days with extremes of 1 day and 60 days. The anatomical location of the lesions is given in <xref ref-type="table" rid="table3">Table 3</xref>.</p><p>The most frequent clinical signs were pain and infectious syndrome (100%), necrotic (47%) and ulcerative-necrotic lesions (53%). Ten patients (24.39%) experienced septic shock.</p><p>Therapeutically, all the patients benefited from resuscitation, bi or triantibiotherapy and surgical debridement in the operating room. Antibiotic therapy included a third-generation cephalosporin, an imidazole, and an aminoglycoside if kidney function was good. Only 4 patients required two debridements in the operating room. A suprapubic cystostomy was performed in 4 (9.76%) patients. No colostomy was performed. Five patients benefited from secondary suturing distant from infectious phenomena.</p><p>Postoperative mortality was 24.39% (10/41). The average age of the deceased patients was 70 years. There was no statistically significant difference between the ages of the survivors and the ages of the deceased (p = 0.180). The average consultation time was 19 days in the deceased versus 14.37 days in the survivors but with no statistically significant difference (p = 0.455). We noted that the mortality rate was higher in patients who had a hemoglobin level lower than 10 g/dl compared to those who had a hemoglobin level higher than 10 g/dl (p = 0.008). The mean hospital stay was 10.83 &#177; 6.257 days with extremes of 1 day and 25 days.</p><p><xref ref-type="table" rid="table4">Table 4</xref> gives the comparison of clinical and biological elements between the series of mortality and survival.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Distribution of patients according to the risk factors</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Risk factors</th><th align="center" valign="middle" >Effective</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >HBP Paraplegia Diabetes HIV Sickle cell anemia Renal failure Idiopathic</td><td align="center" valign="middle" >9 4 2 1 1 1 23</td><td align="center" valign="middle" >22 9.8 4.9 2.4 2.4 2.4 56.1</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >41</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><p>HBP: Hight Blood Pressuer, HIV: Human Immuno-defiency virus.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Distribution of patients according to etiologies</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Etiologies</th><th align="center" valign="middle" ></th><th align="center" valign="middle" >Effectif</th><th align="center" valign="middle" >Percentage</th></tr></thead><tr><td align="center" valign="middle" >Urological (36.58%)</td><td align="center" valign="middle" >Scrotal abscess Infected hydrocele Urethral stenosis Benign prostatic hyperpasia Bladder tumor</td><td align="center" valign="middle" >3 4 4 3 1</td><td align="center" valign="middle" >4.88 9.75 7.32 4.88 2.44</td></tr><tr><td align="center" valign="middle" >Proctological (4.88%)</td><td align="center" valign="middle" >Perianal abscess</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >4.88</td></tr><tr><td align="center" valign="middle" >Iatrogenic (12.20%)</td><td align="center" valign="middle" >Post-prostatic adenomectomy Post-hydrocelectomy</td><td align="center" valign="middle" >2 3</td><td align="center" valign="middle" >4.88 7.32</td></tr><tr><td align="center" valign="middle" >Traumatic (2.44%)</td><td align="center" valign="middle" >Scrotal trauma</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >2.44</td></tr><tr><td align="center" valign="middle" >Dermatological (14.63%)</td><td align="center" valign="middle" >Bedsores Scrotal boil</td><td align="center" valign="middle" >4 2</td><td align="center" valign="middle" >9.76 4.88</td></tr><tr><td align="center" valign="middle" >No cause found (29.27%)</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >12</td><td align="center" valign="middle" >29.27</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" ></td><td align="center" valign="middle" >41</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 the extent of the lesions</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >location of lesions</th><th align="center" valign="middle" >Effective</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Scrotum</td><td align="center" valign="middle" >25</td><td align="center" valign="middle" >61</td></tr><tr><td align="center" valign="middle" >Perineo-scotal</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >19.5</td></tr><tr><td align="center" valign="middle" >Penis</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >7.3</td></tr><tr><td align="center" valign="middle" >Scrotum and penis</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >9.8</td></tr><tr><td align="center" valign="middle" >pubis</td><td align="center" valign="middle" >1</td><td align="center" valign="middle" >2.4</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >41</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Comparison of clinical and biological elements between survivors and deceased</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Survivants N = 31</th><th align="center" valign="middle" >D&#233;c&#233;d&#233;s N = 10</th><th align="center" valign="middle" >Valeur p</th></tr></thead><tr><td align="center" valign="middle" >Age Consultation period Septic shock Duration of hospitalization Comorbidities present</td><td align="center" valign="middle" >63.42 (&#177;16.39) 14.37 (&#177;15.27) 7.5% 9.90 (&#177;5.31) 48.39%</td><td align="center" valign="middle" >70.00 (&#177;22.24) 19 (&#177;18.93) 17.5% 13.70 (8.25) 16.67%</td><td align="center" valign="middle" >0.319 0.455 0.001 0.096 0.467</td></tr><tr><td align="center" valign="middle" >Hemoglobin level &lt;10 g/dl &gt;10 g/dl Creatinine</td><td align="center" valign="middle" >160.16 (&#177;155.78)</td><td align="center" valign="middle" >50% 9.09% 214.98 (&#177;128.91)</td><td align="center" valign="middle" >0.008 0.355</td></tr></tbody></table></table-wrap></sec><sec id="s4"><title>4. Discussion</title><p>In our series the GOGE hospital frequency was 0.54%. In the United States Sorensen estimated its frequency to be less than 0.02% [<xref ref-type="bibr" rid="scirp.100159-ref5">5</xref>]. In the Kambou series in Burkina Faso, the GOGE represented 2.3% of hospitalizations [<xref ref-type="bibr" rid="scirp.100159-ref6">6</xref>]. In other words, it is a rare condition. However, the most important series come from developing countries [<xref ref-type="bibr" rid="scirp.100159-ref1">1</xref>].</p><p>All of our patients were male. Indeed, GOGE is known to be a condition which mainly affects the male subject. Most studies on the issue point to the clear male dominance [<xref ref-type="bibr" rid="scirp.100159-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.100159-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.100159-ref9">9</xref>]. This is explained by the fact that in women there is better drainage of the perineal region through the vaginal secretions [<xref ref-type="bibr" rid="scirp.100159-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.100159-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.100159-ref11">11</xref>]. Y&#252;cell, on the other hand, reports in its series a female predominance at 56% [<xref ref-type="bibr" rid="scirp.100159-ref12">12</xref>].</p><p>GOGE was initially described by Jean Alfred Fournier as an affection of the young subject. But nowadays there is a change in the age of onset of this condition which reaches 61.7 years in certain series [<xref ref-type="bibr" rid="scirp.100159-ref13">13</xref>]. This would be linked to the increase in life expectancy. The average age of our patients was 65.65 &#177; 17.69 years with extremes of 23 and 95 years. Our study effectively confirms this evolution in the epidemiology of GOGE. Older age has been reported as a factor of poor prognosis in GOGE [<xref ref-type="bibr" rid="scirp.100159-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.100159-ref15">15</xref>]. In our series, however, we did not find a statistically significant difference between the age of the survivors and that of the deceased (p = 0.180).</p><p>In our series, high blood pressure was the most common comorbidity with 22% of cases. In addition, there were two cases of diabetes and one case of infection with the human immunodeficiency virus. What is decisive in these comorbidities is the decrease in cellular immunity which thus promotes infection [<xref ref-type="bibr" rid="scirp.100159-ref9">9</xref>]. However, there was no statistically significant difference between the survivors and the deceased concerning the presence or not of co-morbidity (p = 0.467). Four patients were paraplegic in our series. Spinal cord injured people are three times more likely to develop GOGE during their lifetime due to pressure ulcers and chronic urethral catheterization [<xref ref-type="bibr" rid="scirp.100159-ref10">10</xref>].</p><p>The three major etiological groups in GOGE are urogenital, proctological and dermatological [<xref ref-type="bibr" rid="scirp.100159-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.100159-ref9">9</xref>]. In our series gangrene without recognized cause represented 29.27% of cases. This high rate of gangrene without recognized cause could be explained by the lack of means of exploration in our context. Indeed, nowadays a cause is almost always identified in the GOGE [<xref ref-type="bibr" rid="scirp.100159-ref16">16</xref>]. Urological causes predominated in our series with 36.58% of cases. Fall in Senegal found a similar result [<xref ref-type="bibr" rid="scirp.100159-ref14">14</xref>]. We noted 5 cases (12.19%) of iatrogenic GOGE following a hydrocelectomy (3 cases) and a transvesical prostatic adenectomy (2 cases). Our result is higher than that of Ersay in Turkey who reported 2.9% postoperative gangrene in his series [<xref ref-type="bibr" rid="scirp.100159-ref17">17</xref>].</p><p>The mean consultation time for the deceased (19 days) was higher than that for the survivors (14.37 days), but the difference was not statistically significant (p = 0.455). Lujan Marco in Spain made the same observation [<xref ref-type="bibr" rid="scirp.100159-ref2">2</xref>]. However, some have established that rapid management is a good prognostic factor in GOGE [<xref ref-type="bibr" rid="scirp.100159-ref18">18</xref>]. Unfortunately, as Ruiz-Tovar pointed out, the period of consultation does not depend on the medical profession [<xref ref-type="bibr" rid="scirp.100159-ref19">19</xref>]. In our context, populations rarely consult health structures in the first place.</p><p>GOGE is a urological emergency whose treatment consists of a therapeutic tripod: resuscitation, triple antibiotic therapy and surgical debridement [<xref ref-type="bibr" rid="scirp.100159-ref20">20</xref>]. All our patients benefited from surgical debridement after resuscitation and bi or tri-antibiotic therapy. A first aggressive debridement often avoids a second intervention in the operating room [<xref ref-type="bibr" rid="scirp.100159-ref3">3</xref>].</p><p>GOGE’s prognosis remains poor despite improved resuscitation facilities. Mortality varies between 16% and 40% and can go up to 80% in certain series [<xref ref-type="bibr" rid="scirp.100159-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.100159-ref8">8</xref>]. The mortality rate in our series was 24.39%. This means that about a quarter of our patients die. This result is clearly higher than that of Kambou, who noted a mortality rate of 5.5% [<xref ref-type="bibr" rid="scirp.100159-ref6">6</xref>]. This could be explained by the long consultation period in our series but also and above all by an inadequate resuscitation linked to the lack of biological explorations. There is still controversy as to the factors that influence mortality in GOGE [<xref ref-type="bibr" rid="scirp.100159-ref17">17</xref>]. Several prognostic factors have been reported. These include advanced age, diabetes, delay in treatment, and certain biological parameters [<xref ref-type="bibr" rid="scirp.100159-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.100159-ref19">19</xref>]. We were unable to establish prognostic scores in our series due to the unavailability of biochemical examinations in our health structure. This is a limiting factor in the correction of hydro-electrolytic disorders of our patients. However, we were able to demonstrate that the presence of septic shock as well as anemia was factors of poor prognosis in our series. Indeed, we noted that the mortality rate was higher in patients who had a hemoglobin level lower than 10 g/dl compared to those who had a hemoglobin level higher than 10 g/dl (p = 0.008). Ruiz-Tovar has shown that the risk of dying is 9.6 times higher if the hemoglobin level is less than 10 g/dl [<xref ref-type="bibr" rid="scirp.100159-ref19">19</xref>].</p><p>We did not find a statistically significant link between the survivors and the deceased with regard to serum creatinine (p = 0.072). Unlike our study, several studies have shown that elevated serum creatinine is associated with high mortality [<xref ref-type="bibr" rid="scirp.100159-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.100159-ref19">19</xref>].</p></sec><sec id="s5"><title>5. Conclusion</title><p>GOGE still has very high lethality. Contrary to the initial description made by Jean Alfred Fournier, GOGE occurs today at an advanced age in patients with low immunity. Several factors determine its prognosis. But in our context, it is mainly the delayed diagnosis which seems to be the main factor. Thus, health education as well as an improvement of the technical platform with a resuscitation service will improve the prognosis of this condition.</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>Traore, T.M., Yameogo, C.A.M.K.D., Kabore, M. and Ouedraogo, S. (2020) Gangrene of the External Genitalia at the Regional University Hospital Center of Ouahigouya: Epidemiological Profile and Therapeutic Aspects. Open Journal of Urology, 10, 184-191. https://doi.org/10.4236/oju.2020.106021</p></sec></body><back><ref-list><title>References</title><ref id="scirp.100159-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Sarkis, P., Farranc, F., Khoury, R., Kamel, G., Nemr, E., Biajini, J. and Merheje, S. (2009) Gangrène de Fournier: Revue de la littérature récente. Progrès en Urologie, 19, 75-84. https://doi.org/10.1016/j.purol.2008.09.050</mixed-citation></ref><ref id="scirp.100159-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Luján Marco, S., Budía, A., Di Capua, C., Broseta, E. and Jiménez Cruz, F. (2010) Evaluation of a Severity Score to Predict the Prognosis of Fournier’s Gangrene. 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