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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">JCCI</journal-id>
      <journal-title-group>
        <journal-title>Journal of Clinical Case Reports and Images</journal-title>
      </journal-title-group>
      <issn pub-type="epub">2641-5518</issn>
      <publisher>
        <publisher-name>Open Access Pub</publisher-name>
        <publisher-loc>United States</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.14302/issn.2641-5518.jcci-22-4096</article-id>
      <article-id pub-id-type="publisher-id">JCCI-22-4096</article-id>
      <article-categories>
        <subj-group>
          <subject>case-report </subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Duodenocolic Fistula: A Rare Complication of Gastrointestinal Tuberculosis </article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Julian</surname>
            <given-names>Iñaki L. Garcia</given-names>
          </name>
          <xref ref-type="aff" rid="idm1841626596">1</xref>
          <xref ref-type="aff" rid="idm1841626020">*</xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Ronald</surname>
            <given-names>V. Romero</given-names>
          </name>
          <xref ref-type="aff" rid="idm1841626596">1</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1841626596">
        <label>1</label>
        <addr-line>Department of Gastroenterology, De La Salle University Medical Center</addr-line>
      </aff>
      <aff id="idm1841626020">
        <label>*</label>
        <addr-line>Corresponding author</addr-line>
      </aff>
      <contrib-group>
        <contrib contrib-type="editor">
          <name>
            <surname>Carlo</surname>
            <given-names>Aprile</given-names>
          </name>
          <xref ref-type="aff" rid="idm1841744156">1</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1841744156">
        <label>1</label>
        <addr-line>IRCCS Fond. Policlinico San               Matteo - Pavia-Italy.</addr-line>
      </aff>
      <author-notes>
        <corresp>
    
    Julian Iñaki L. Garcia, <addr-line>Department of                        Gastroenterology, De La Salle University Medical Center</addr-line><email>jakkigarcia12@gmail.com</email></corresp>
        <fn fn-type="conflict" id="idm1850785572">
          <p>The authors have declared that no competing interests exist.</p>
        </fn>
      </author-notes>
      <pub-date pub-type="epub" iso-8601-date="2022-03-11">
        <day>11</day>
        <month>03</month>
        <year>2022</year>
      </pub-date>
      <volume>2</volume>
      <issue>2</issue>
      <fpage>20</fpage>
      <lpage>25</lpage>
      <history>
        <date date-type="received">
          <day>08</day>
          <month>02</month>
          <year>2022</year>
        </date>
        <date date-type="accepted">
          <day>05</day>
          <month>03</month>
          <year>2022</year>
        </date>
        <date date-type="online">
          <day>11</day>
          <month>03</month>
          <year>2022</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>© </copyright-statement>
        <copyright-year>2022</copyright-year>
        <copyright-holder>Julian Iñaki L. Garcia, et al.</copyright-holder>
        <license xlink:href="http://creativecommons.org/licenses/by/4.0/" xlink:type="simple">
          <license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
        </license>
      </permissions>
      <self-uri xlink:href="http://openaccesspub.org/jcci/article/1796">This article is available from http://openaccesspub.org/jcci/article/1796</self-uri>
      <abstract>
        <sec id="idm1841474236">
          <title>Introduction </title>
          <p>Benign duodenocolic fistula (DCF), also known as a non-malignant fistula between the      duodenum and colon, with or without                      cecum-involvement, is an unusual complication of different gastrointestinal (GI) diseases <xref ref-type="bibr" rid="ridm1850569788">1</xref><xref ref-type="bibr" rid="ridm1850575916">2</xref>. </p>
        </sec>
        <sec id="idm1841471428">
          <title>Case</title>
          <p>This is a case of a 28-year-old Filipino  female who presented with periumbilical pain for five months, with associated anorexia, fever, and weight loss. Biopsy showed chronic granulomatous inflammation with caseation necrosis and Langhan’s type giant cells consistent with tuberculous etiology (<xref ref-type="fig" rid="idm1841738452">Figure 6</xref> and <xref ref-type="fig" rid="idm1841679420">Figure 7</xref>). Category I Anti-TB treatment for six months was started and the service planned to repeat both colonoscopy and CT-scan after the initial round of anti-TB treatment.</p>
        </sec>
        <sec id="idm1841472148">
          <title>Conclusion </title>
          <p>Benign duodenocolic fistula in the form of extrapulmonary TB is a rare GI finding that is               triggered by inflammatory processes. Proper                  management in this case was to treat the underlying TB infection which is endemic in the Philippines. </p>
        </sec>
      </abstract>
      <kwd-group>
        <kwd>Benign Duodenocolic Fistula</kwd>
        <kwd>Tuberculosis</kwd>
        <kwd>Gastrointestinal Tuberculosis</kwd>
      </kwd-group>
      <counts>
        <fig-count count="7"/>
        <table-count count="0"/>
        <page-count count="6"/>
      </counts>
    </article-meta>
  </front>
  <body>
    <sec id="idm1841478988" sec-type="intro">
      <title>Introduction </title>
      <p>Duodenocolic fistula secondary to tuberculosis is a rare entity. There is a myriad of etiologies for fistula formation, among those reported include           malignancy, previous abdominal surgery,                        inflammatory bowel disease (IBD), cystic fibrosis, and tuberculosis (TB) <xref ref-type="bibr" rid="ridm1850569788">1</xref>.</p>
      <p>A benign duodenocolic fistula is also known as a tract between the duodenum and colon or the cecum with non-malignant origin. These fistulas are less common than malignant fistulas and may be          secondary to peptic ulcer disease (PUD), biliary tract disease, ulcerative colitis, regional enteritis,            appendicitis, caseating tuberculous lymph nodes, or perforating duodenal diverticula <xref ref-type="bibr" rid="ridm1850575916">2</xref>,<xref ref-type="bibr" rid="ridm1850673396">3</xref>. In the Philippines, TB is endemic and there are a small number of cases that involve extrapulmonary TB, including gastrointestinal (GI) TB. This report presents a rare case of a duodenocolic  fistula, which to the extent of the authors' knowledge, is the first case reported in the region.</p>
    </sec>
    <sec id="idm1841477908" sec-type="cases">
      <title>Case Report</title>
      <p>This is a case of a 28-year-old Filipino female who presented with periumbilical pain for five months, with associated anorexia, fever, and weight loss in the                subsequent days. Three days prior to admission, patient noted an onset of hematochezia and hematemesis.              Examination of the abdomen noted hyperactive bowel sounds and tender periumbilical and right lower quadrant pain, and no organomegaly was noted. </p>
      <p>Esophagogastroduodenoscopy (EGD) revealed a fistulous opening in the third part of the duodenum and a bleeding vessel. (<xref ref-type="fig" rid="idm1841744140">Figure 1</xref>) Bleeding was controlled with injection hemostasis and 3 hemoclips were deployed. The colonoscopy revealed a large obstructing, polypoid,           ulcerating, and circumferential mass with areas of              necrosis that was seen at the proximal transverse colon which precluded further advancement of the scope. Biopsy samples were sent for histopathology investigation and TB polymerase chain reaction (PCR) test.</p>
      <fig id="idm1841744140">
        <label>Figure 1.</label>
        <caption>
          <title> EGD findings of a pathologic lumen and a bleeding vessel were seen at the third portion of the            duodenum.</title>
        </caption>
        <graphic xlink:href="images/image1.jpg" mime-subtype="jpg"/>
      </fig>
      <p>There was no evidence of malignancy or IBD seen during both endoscopic procedures. Computed                     tomography (CT) scan of the whole abdomen was done which showed inflammatory changes involving the cecum and adjacent duodenum and ileum with coloenteric            fistulae. There was noted progression of abdominal            lymphadenopathies as well as ascites. Main consideration was an infectious disease process (i.e. TB) (<xref ref-type="fig" rid="idm1841742556">Figure 2</xref>, <xref ref-type="fig" rid="idm1841742916">Figure 3</xref>, <xref ref-type="fig" rid="idm1841741188">Figure 4</xref> to <xref ref-type="fig" rid="idm1841740684">Figure 5</xref>).</p>
      <fig id="idm1841742556">
        <label>Figure 2.</label>
        <caption>
          <title> Colonoscopy finding of a circumferential, obstructive and nodular mass with areas of  necrosis with a pathologic lumen believed to be communicating with the lumen seen on the previous EGD was seen at the proximal transverse which precluded further advancement of the scope </title>
        </caption>
        <graphic xlink:href="images/image2.jpg" mime-subtype="jpg"/>
      </fig>
      <fig id="idm1841742916">
        <label>Figure 3.</label>
        <caption>
          <title> Coronal and axial view of the abdomen, the blue arrows pointing towards the suggestive                     communication to the ileum.</title>
        </caption>
        <graphic xlink:href="images/image3.jpg" mime-subtype="jpg"/>
      </fig>
      <fig id="idm1841741188">
        <label>Figure 4.</label>
        <caption>
          <title> Coronal and axial view of the abdomen, the blue arrows pointing towards the suggestive             communication to the duodenum </title>
        </caption>
        <graphic xlink:href="images/image4.jpg" mime-subtype="jpg"/>
      </fig>
      <fig id="idm1841740684">
        <label>Figure 5.</label>
        <caption>
          <title> Enlarged and necrotic abdominal nodes in the mesenteric, pericecal, pericolic, para-aortic, paracaval and inter-aortocaval regions. Prominent and enlarged nodes also located in the common hepatic and periportal regions</title>
        </caption>
        <graphic xlink:href="images/image5.jpg" mime-subtype="jpg"/>
      </fig>
      <p>Biopsy showed chronic granulomatous                    inflammation with caseation necrosis and Langhan’s type giant cells consistent with tuberculous etiology (<xref ref-type="fig" rid="idm1841738452">Figure 6</xref>, and <xref ref-type="fig" rid="idm1841679420">Figure 7</xref>). TB PCR detected Mycobacterium tuberculosis,     Rifampicin (MTB, RIF) resistance indeterminate. Category I Anti-TB treatment for six months was started and the service planned to repeat both colonoscopy and CT-scan after the initial round of anti-TB treatment. Currently, the patient is able to work with no abdominal pain and was able to tolerate her anti-TB drug regimen </p>
      <fig id="idm1841738452">
        <label>Figure 6.</label>
        <caption>
          <title> Pathologic slide in the low power field. The area inside the yellow circle is the area of central necrosis. The portion inside the red circle is the peripheral lymphocytic ring, and inside the green circle is the Langhan’s type multinucleated giant cells </title>
        </caption>
        <graphic xlink:href="images/image6.jpg" mime-subtype="jpg"/>
      </fig>
      <fig id="idm1841679420">
        <label>Figure 7.</label>
        <caption>
          <title> Pathologic slide in the high power field. Inside the green circle is the epitheloid histiocytes. The yellow circles are the Langhan’s type multinucleated gian cells. And inside the red circle is the                        lymphocytic infiltrates. Which is suggestive of tuberculous etiology. </title>
        </caption>
        <graphic xlink:href="images/image7.jpg" mime-subtype="jpg"/>
      </fig>
    </sec>
    <sec id="idm1841463228" sec-type="discussion">
      <title>Discussion </title>
      <p>Benign duodenocolic fistula is a complication that occurs through a perforation between the duodenum and the mid-transverse column, due to the presence of a               duodenal diverticulum <xref ref-type="bibr" rid="ridm1850673396">3</xref>. This condition is often due to inflammatory diseases of the gastrointestinal tract such as gallstone disease. Crohn’s disease, and even                                  Tuberculosis <xref ref-type="bibr" rid="ridm1850427372">4</xref>. In some studies, duodenocolic fistulas have been noted as a type of inflammatory response to colon cancer, duodenal cancer, and peptic ulcer disease, among others <xref ref-type="bibr" rid="ridm1850569788">1</xref>, <xref ref-type="bibr" rid="ridm1850427372">4</xref>. </p>
      <p>Benign duodenocolic fistulas feature colicky             abdominal pain, diarrhea, nausea and vomiting as                 common non-specific symptoms <xref ref-type="bibr" rid="ridm1850575916">2</xref>,<xref ref-type="bibr" rid="ridm1850673396">3</xref>, <xref ref-type="bibr" rid="ridm1850427372">4</xref> The diagnosis of this condition can include upper gastrointestinal                  barium studies or a barium enema; however, endoscopic evaluation is necessary in proper diagnosis as allows                better visualization of the mass, as well as the areas                 adjacent to it <xref ref-type="bibr" rid="ridm1850575916">2</xref>, <xref ref-type="bibr" rid="ridm1850427372">4</xref>. Surgery is the only treatment that could be called a cure for this condition, and En-bloc              resection of the tumor-fistula complex is the definitive management of duodenocolic fistulas <xref ref-type="bibr" rid="ridm1850673396">3</xref>. For those with advanced lesions, palliative care may be the best                        solution <xref ref-type="bibr" rid="ridm1850673396">3</xref>.</p>
      <p>Tuberculosis-associated duodenocolic fistula is an extremely rare finding among the general population. This case is the first reported for this region of the Philippines. In Gan et al, 2021, it was found that a patient’s previous history of pulmonary tuberculosis was the culprit behind their own illness <xref ref-type="bibr" rid="ridm1850569788">1</xref>. Abdominal TB may occur as diffuse, white to yellowish peritoneal nodules and ascitic                    adenosine deaminase  (ADA)  highly sensitive to TB <xref ref-type="bibr" rid="ridm1850569788">1</xref>. In countries where TB is endemic, patients are usually            started on anti-TB medication as soon as possible. The initiation and continuation of anti-TB medications should be done, and these remain the “cornerstone” of TB                  treatment even in extrapulmonary cases such as this               one<xref ref-type="bibr" rid="ridm1850569788">1</xref><xref ref-type="bibr" rid="ridm1850673396">3</xref>.</p>
    </sec>
    <sec id="idm1841463732" sec-type="conclusions">
      <title>Conclusion </title>
      <p>Benign duodenocolic fistula in the form of                extrapulmonary TB is a rare GI finding that is triggered by inflammatory processes. Proper management in this case was to treat the underlying TB infection which is endemic in the Philippines. </p>
    </sec>
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