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<art>
   <ui>1757-1626-2-53</ui>
   <ji>1757-1626</ji>
   <fm>
      <dochead>Case Report</dochead>
      <bibl>
         <title>
            <p>A rare presentation of appendicitis as groin swelling: a case report</p>
         </title>
         <aug>
            <au id="A1" ca="yes">
               <snm>Pitchaimuthu</snm>
               <fnm>Maheswaran</fnm>
               <insr iid="I1"/>
               <insr iid="I2"/>
               <email>drmpitchaimuthu@yahoo.com</email>
            </au>
            <au id="A2">
               <snm>Dace</snm>
               <fnm>Stephen</fnm>
               <insr iid="I1"/>
               <insr iid="I3"/>
               <email>Stephen.Dace@westerntrust.hscni.net</email>
            </au>
         </aug>
         <insg>
            <ins id="I1">
               <p>Department of General Surgery, Altnagelvin Area Hospital, Londonderry, Northern Ireland, UK</p>
            </ins>
            <ins id="I2">
               <p>SpR in HPB Surgery, Imperial College Healthcare NHS Trust, Hammersmith Hospital, London, W12 0HS, UK</p>
            </ins>
            <ins id="I3">
               <p>Consultant Surgeon, Western Health and Social Care Trust, Altnagelvin Hospital, Londonderry, BT47 6SB, UK</p>
            </ins>
         </insg>
         <source>Cases Journal</source>
         <issn>1757-1626</issn>
         <pubdate>2009</pubdate>
         <volume>2</volume>
         <issue>1</issue>
         <fpage>53</fpage>
         <url>http://www.casesjournal.com/content/2/1/53</url>
         <xrefbib>
            <pubidlist>
               <pubid idtype="pmpid">19144175</pubid>
               <pubid idtype="doi">10.1186/1757-1626-2-53</pubid>
            </pubidlist>
         </xrefbib>
      </bibl>
      <history>
         <rec>
            <date>
               <day>12</day>
               <month>10</month>
               <year>2008</year>
            </date>
         </rec>
         <acc>
            <date>
               <day>14</day>
               <month>1</month>
               <year>2009</year>
            </date>
         </acc>
         <pub>
            <date>
               <day>14</day>
               <month>1</month>
               <year>2009</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>2009</year>
         <collab>Pitchaimuthu and Dace; licensee BioMed Central Ltd.</collab>
         <note>This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</note>
      </cpyrt>
      <abs>
         <sec>
            <st>
               <p>Abstract</p>
            </st>
            <sec>
               <st>
                  <p>Background</p>
               </st>
               <p>Appendicitis in femoral hernia is a rare condition, which raises diagnostic challenge.</p>
            </sec>
            <sec>
               <st>
                  <p>Case Report</p>
               </st>
               <p>A 40-year-old man presented with painful right-sided groin swelling of 1-week duration. The area was explored, with presumpted diagnosis of inguinal abscess. At exploration a femoral hernia was found which contained a mildly inflammed appendix. Appendicectomy and hernia repair was done. Post surgical course was uneventful. We present this case with brief summary of literature pertaining to such lesions.</p>
            </sec>
            <sec>
               <st>
                  <p>Discussion</p>
               </st>
               <p>The rare occurrence of femoral hernia containing appendix may be explained by different degrees of intestinal rotation during development or variation in its attachment to the caecum. Inflammation is due to tight femoral ring. Preoperative diagnosis is difficult. Management options are diverse.</p>
            </sec>
            <sec>
               <st>
                  <p>Conclusion</p>
               </st>
               <p>We present this case because of rarity. Early surgery prevents complications.</p>
            </sec>
         </sec>
      </abs>
   </fm>
   <bdy>
      <sec>
         <st>
            <p>Introduction</p>
         </st>
         <p>Inflammatory swellings of the groin are common, and the changes are often attributed to infection. Although this is possible, inflammatory swellings are often secondary to groin hernia. We present an unusual case of groin swelling, outlining its investigations and subsequent management.</p>
      </sec>
      <sec>
         <st>
            <p>Case report</p>
         </st>
         <p>An otherwise healthy 40-year-old male presented with a one-week history of pain and swelling in his right groin. There was no history of trauma or previous hernia, and his bowel habit was normal. On examination he had a right inguinal swelling (6 &#215; 3 cm) lateral to the pubic tubercle. There was no evidence of a cough impulse.</p>
         <p>An ultrasound of the region was performed (Figure <figr fid="F1">1</figr>), which showed evidence of cellulitis and a fluid collection. The fluid was aspirated; it was blood stained with no evidence of pus. Routine blood tests were normal.</p>
         <fig id="F1">
            <title>
               <p>Figure 1</p>
            </title>
            <caption>
               <p>USS right groin showing fluid collection</p>
            </caption>
            <text>
               <p><b>USS right groin showing fluid collection</b>.</p>
            </text>
            <graphic file="1757-1626-2-53-1"/>
         </fig>
         <p>Given the clinical findings, he was taken to the operating theatre for exploration. A standard oblique groin incision was used, and an incarcerated femoral hernia was identified. The back of the inguinal canal and the neck of the sac were opened. Inside the sac, a long, mildly inflamed appendix was found (Figure <figr fid="F2">2</figr>). An appendicectomy was performed and the excess sac excised and transfixed. Given that there was minimal inflammation of the appendix and there was no obvious evidence of infection outside the sac, the back wall of the inguinal canal was repaired using the Lichtenstein tension-free mesh method, using 15 &#215; 7 cm Vypro Mesh and 2-0 prolene. The patient had an uneventful recovery.</p>
         <fig id="F2">
            <title>
               <p>Figure 2</p>
            </title>
            <caption>
               <p>Intra operative picture showing appendix in femoral hernia sac</p>
            </caption>
            <text>
               <p><b>Intra operative picture showing appendix in femoral hernia sac</b>.</p>
            </text>
            <graphic file="1757-1626-2-53-2"/>
         </fig>
      </sec>
      <sec>
         <st>
            <p>Discussion</p>
         </st>
         <p>The main pathologic conditions manifesting as masses in the groin fall into five major groups: congenital abnormalities, non-congenital hernias, vascular conditions, infectious or inflammatory processes, and neoplasms <abbrgrp><abbr bid="B1">1</abbr><abbr bid="B2">2</abbr></abbrgrp>. The hernial sac may contain preperitoneal fat, omentum, colon, or small bowel but reports of femoral hernia containing the vermiform appendix are rare, reported to occur in 0.8% of femoral hernia <abbrgrp><abbr bid="B3">3</abbr></abbrgrp>. Rence Jacques Croissant de Garengeot, an 18<sup>th </sup>century Paris Surgeon, was the first to describe appendix in femoral hernia <abbrgrp><abbr bid="B4">4</abbr></abbrgrp>. Appendix in left femoral hernia <abbrgrp><abbr bid="B5">5</abbr></abbrgrp>, carcinoid tumour of appendix <abbrgrp><abbr bid="B6">6</abbr></abbrgrp> and stomach <abbrgrp><abbr bid="B7">7</abbr></abbrgrp> as femoral hernia contents have also been reported in the past. Factors contributing to this condition include degrees of intestinal malrotation or the presence of an abnormally large caecum which extends into the pelvis <abbrgrp><abbr bid="B3">3</abbr></abbrgrp>.</p>
         <p>It is very difficult to diagnose the presence of an appendix within a femoral hernial sac, and to date, only one case has been diagnosed prior to surgery. This was identified at CT scan <abbrgrp><abbr bid="B8">8</abbr></abbrgrp>.</p>
         <p>Tight femoral ring leads to strangulation and appendicitis. Appendicitis in a femoral hernia does not usually lead to abdominal peritonitis, due to narrow hernia sac neck which prevents inflammation of the parietal peritoneum. Clinical signs include local groin swelling, inflammation and spreading cellulitis, but often the patient feels generally well with no systemic features of sepsis, as in this case <abbrgrp><abbr bid="B3">3</abbr></abbrgrp>.</p>
         <p>If left untreated, the inflammation may resolve or lead to complications including abscess <abbrgrp><abbr bid="B9">9</abbr></abbrgrp>, necrotizing fasciitis <abbrgrp><abbr bid="B10">10</abbr></abbrgrp>, necrosis of hernial contents <abbrgrp><abbr bid="B11">11</abbr></abbrgrp> and development of bowel obstruction <abbrgrp><abbr bid="B12">12</abbr></abbrgrp> and even death.</p>
         <p>Due to the rarity of such cases treatment options remain diverse. Each case should be judged separately, and treatment based on the principles of removing the source of sepsis (either operatively or by aspiration) should be employed <abbrgrp><abbr bid="B13">13</abbr><abbr bid="B14">14</abbr></abbrgrp>.</p>
      </sec>
      <sec>
         <st>
            <p>Conclusion</p>
         </st>
         <p>We present a case of acute appendicitis complicating an incarcerated femoral hernia. As is often the case, the diagnosis was made at surgery. By following the principles of removing the source of sepsis and repairing the hernial defect, the patient made a safe recovery from a potentially serious condition.</p>
         <p>We present this case because of appendix in femoral hernia that too in a young male patient is very rare. Early surgical treatment prevents potential complications.</p>
      </sec>
      <sec>
         <st>
            <p>Consent</p>
         </st>
         <p>A written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor in Chief of this journal.</p>
      </sec>
      <sec>
         <st>
            <p>Competing interests</p>
         </st>
         <p>The authors declare that they have no competing interests.</p>
      </sec>
      <sec>
         <st>
            <p>Authors' contributions</p>
         </st>
         <p>MP was the oncall registrar, who performed the surgery and a primary author for this manuscript. SD was the oncall consultant who was a contributor in writing the manuscript.</p>
      </sec>
   </bdy>
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