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 <front>
  <journal-meta>
   <journal-id journal-id-type="nlm-ta">Ulutas Med J</journal-id>
   <journal-title-group>
    <journal-title>The Ulutas Medical Journal</journal-title>
    <abbrev-journal-title>Ulutas Med J</abbrev-journal-title>
   </journal-title-group>
   <issn pub-type="ppub">2149-0430</issn>
   <issn pub-type="epub">2149-388X</issn>
   <publisher>
    <publisher-name>Hayriye Zehra Ulutaş</publisher-name>
   </publisher>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="doi">10.5455/umj.20220222072137</article-id>
   <article-id pub-id-type="publisher-id">87160</article-id>
   <article-categories>
    <subj-group subj-group-type="heading">
     <subject>Case Report</subject>
    </subj-group>
    <subj-group subj-group-type="subject">
     <subject>Cancer</subject>
    </subj-group>
   </article-categories>
   <title-group>
    <article-title>Intrabiliary Metastasis of Colon Cancer Mimicking Cholangiocarcinoma and Chemotherapy-Induced Sclerosing Cholangitis: A Case Report</article-title>
   </title-group>
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     <name name-style="western">
      <surname>Chen</surname>
      <given-names>Po-Yuan</given-names>
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     <name name-style="western">
      <surname>Lee</surname>
      <given-names>Guang-Mao</given-names>
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    <aff id="aff1">
     <label>1</label>
     <institution-wrap>
      <institution-id institution-id-type="ror">https://ror.org/02y2htg06</institution-id>
      <institution>Department of Radiology, Chi Mei Medical Center, Liouying, Tainan, Taiwan</institution>
     </institution-wrap>
    </aff>
    <aff id="aff2">
     <label>2</label>
     <institution-wrap>
      <institution-id institution-id-type="ror">https://ror.org/02y2htg06</institution-id>
      <institution>Department of Intensive Care Medicine, Chi Mei Medical Center, Liouying, Tainan, Taiwan</institution>
     </institution-wrap>
    </aff>
    <aff id="aff3">
     <label>3</label>
     <institution-wrap>
      <institution-id institution-id-type="ror">https://ror.org/03db90279</institution-id>
      <institution>Department of Nursing, Kaohsiung Municipal United Hospital, Taiwan</institution>
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   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2022-06-09">
    <day>09</day>
    <month>06</month>
    <year>2022</year>
   </pub-date>
   <pub-date publication-format="print" date-type="collection">
    <year>2022</year>
   </pub-date>
   <volume>8</volume>
   <issue>2</issue>
   <fpage>82</fpage>
   <lpage>85</lpage>
   <history>
    <date date-type="received" iso-8601-date="2022-02-25">
     <day>25</day>
     <month>02</month>
     <year>2022</year>
    </date>
    <date date-type="rev-recd" iso-8601-date="2022-04-21">
     <day>21</day>
     <month>04</month>
     <year>2022</year>
    </date>
    <date date-type="accepted" iso-8601-date="2022-05-14">
     <day>14</day>
     <month>05</month>
     <year>2022</year>
    </date>
   </history>
   <permissions>
    <copyright-statement>© 2022 The Author(s)</copyright-statement>
    <copyright-year>2022</copyright-year>
    <license>
     <ali:license_ref>https://creativecommons.org/licenses/by-nc/4.0/</ali:license_ref>
     <license-p>This is an open access article distributed under the CC BY-NC 4.0 licence.</license-p>
    </license>
   </permissions>
   <self-uri xlink:href="https://www.ulutasmedicaljournal.com/?mno=87160"/>
   <self-uri content-type="pdf" xlink:href="https://www.ulutasmedicaljournal.com/pdf/87160.pdf"/>
   <abstract>
    <p>Intrabiliary metastasis of colon cancer without the involvement of the hepatic parenchyma is very rare and can cause biliary obstruction. We herein present a rare case of colon cancer metastasis that developed after right hemicolectomy and while undergoing chemotherapy. Computed tomography (CT) of the abdomen and percutaneous transhepatic cholangiography and drainage (PTCD) was performed because of obstructive jaundice. CT-guided biopsy showed high-grade atypical glands that were CK7(â'), CK20(+), and CDX-2(+); metastatic adenocarcinoma would be considered first rather than cholangiocarcinoma. Clinicians should be aware that intrabiliary metastasis of colon cancer can mimic cholangiocarcinoma and chemotherapy-induced sclerosing cholangitis.</p>
   </abstract>
   <kwd-group kwd-group-type="author">
    <kwd>Intrabiliary metastasis</kwd>
    <kwd>colon cancer</kwd>
    <kwd>cholangiocarcinoma</kwd>
   </kwd-group>
   <funding-group>
    <funding-statement>Funding information was not reported in the published version of this article.</funding-statement>
   </funding-group>
  </article-meta>
 </front>
 <body>
  <sec id="sec-1">
   <title>Introduction</title>
   <p id="b-1">Intrabiliary metastasis of colon cancer without involvement of the hepatic parenchyma is rare (    <xref ref-type="bibr" rid="ref1">1</xref>
). Metastases to the liver can cause biliary obstruction and result in painless jaundice, pale stools, dark urine, and pruritis, and such metastases are associated with elevations of direct bilirubin and alkaline phosphatase (    <xref ref-type="bibr" rid="ref2">2</xref>
). In addition, imaging findings showing such metastases as mimicking sclerosing cholangitis as a multifocal biliary stricture are rare. Here, we report a case of intrabiliary metastasis of colon cancer and the associated imaging findings.</p>
  </sec>
  <sec id="sec-2">
   <title>Case Presentation</title>
   <p id="b-2">An 82-year-old man presented with colon metastasis after right hemicolectomy and while undergoing chemotherapy. Laboratory tests at regular follow-up revealed elevated CA19-9 and CEA. Computed tomography (CT) was performed, which revealed soft tissue density in the common bile duct (CBD) and right intrahepatic duct (IHD) with wall thickening, resulting in biliary dilatation (Figures 1 and 2). Percutaneous transhepatic cholangiography and drainage (PTCD) was performed, and cholangiography revealed multiple strictures of the intrahepatic and extrahepatic bile ducts, causing obstructive jaundice (Figure 3). Based on his history and radiological findings, the differential diagnosis included metastasis, chemotherapy-induced sclerosing cholangitis (CISC), and cholangiocarcinoma. Cytology of bile collected from the percutaneous transhepatic drainage tube revealed no features of malignancy. CT-guided biopsy was then performed and revealed high-grade atypical glands. Immunohistochemical study revealed that the atypical glands were CK7(−), CK20(+), and CDX-2(+) (Figure 4).</p>
   <fig id="fig-1" position="float">
    <label>Figure 1</label>
    <caption>
     <p>Axial contrast-enhanced CT showed (a, arrow) soft tissue density in the right anterior intrahepatic bile duct and (b) no intraparenchymal mass</p>
    </caption>
    <graphic xlink:href="fig-1.png">
     <alt-text>Figure 1: Axial contrast-enhanced CT showed (a, arrow) soft tissue density in the right anterior intrahepatic bile duct and (b) no intraparenchymal mass</alt-text>
    </graphic>
   </fig>
   <fig id="fig-2" position="float">
    <label>Figure 2</label>
    <caption>
     <p>(a) Axial and (b) coronal contrast-enhanced CT showed extrahepatic bile duct wall thickening (arrow) with mild dilatation of the biliary system</p>
    </caption>
    <graphic xlink:href="fig-2.png">
     <alt-text>Figure 2: (a) Axial and (b) coronal contrast-enhanced CT showed extrahepatic bile duct wall thickening (arrow) with mild dilatation of the biliary system</alt-text>
    </graphic>
   </fig>
   <fig id="fig-3" position="float">
    <label>Figure 3</label>
    <caption>
     <p>Cholangiography during the PTCD showed multiple strictures of intra-extrahepatic bile ducts (arrow)</p>
    </caption>
    <graphic xlink:href="fig-3.png">
     <alt-text>Figure 3: Cholangiography during the PTCD showed multiple strictures of intra-extrahepatic bile ducts (arrow)</alt-text>
    </graphic>
   </fig>
   <p id="b-3">According to the study result, metastatic adenocarcinoma would be considered first rather than biliary duct primary malignancy given the absence of CK7 expression. The patient’s condition was poor, total bilirubin levels increased again, and liver function worsened, requiring the insertion of two PTCDs on each side. One month later, septic biliary tract infection exacerbated progressively, and the patient finally died.</p>
   <fig id="fig-4" position="float">
    <label>Figure 4</label>
    <caption>
     <p>(a) High-grade atypical glands. ×10; H-E stain. (b), (c), and (d) Immunohistochemical study revealed negative CK7 staining, positive CK20 staining, and positive CDX-2 staining, respectively</p>
    </caption>
    <graphic xlink:href="fig-4.png">
     <alt-text>Figure 4: (a) High-grade atypical glands. ×10; H-E stain. (b), (c), and (d) Immunohistochemical study revealed negative CK7 staining, positive CK20 staining, and positive CDX-2 staining, respectively</alt-text>
    </graphic>
   </fig>
  </sec>
  <sec id="sec-3">
   <title>Discussion</title>
   <p id="b-4">In our case, CT and cholangiography revealed wall thickening of the extrahepatic and intrahepatic bile ducts accompanied by stricture and dilatation. Our case also presented the imaging findings of biliary obstruction and biliary stricture, which are also the imaging findings for secondary sclerosing cholangitis and primary cholangiocarcinoma. CISC has been reported to be occasionally caused by hepatic arterial infusion chemotherapy with fluoropyrimidines (    <xref ref-type="bibr" rid="ref3">3</xref>
–    <xref ref-type="bibr" rid="ref5">5</xref>
). In the study, considering the sudden onset of bile duct lesion during chemotherapy (FOLFOX4), as sclerosing cholangitis was suspected, the patient received initial treatment with steroids, and the chemotherapy was discontinued. However, rapid elevated tumor markers (CEA: 171 ng/mL, CA19-9: 10115 U/mL) and no improvement after cessation of chemotherapy were noted. Distinctive findings of sclerosing cholangitis, such as “onion skin” fibrosis (    <xref ref-type="bibr" rid="ref6">6</xref>
) around the bile duct, were not found in the liver biopsy in our case. Cholangiocarcinoma has the following morphology and growth patterns: mass formation, periductal infiltration, and intraductal growth (    <xref ref-type="bibr" rid="ref7">7</xref>
). The imaging findings of intraductal and periductalinfiltrating type of cholangiocarcinoma included biliary strictures, intraductal neoplasms, and focal or diffuse ductal thickening with or without enhancement (    <xref ref-type="bibr" rid="ref8">8</xref>
,    <xref ref-type="bibr" rid="ref9">9</xref>
). Differentiating intrabiliary colorectal liver metastases from primary intrahepatic cholangiocarcinoma is difficult. However, immunohistochemical studies, such as CK7, CK20, and CDX2 staining, can provide the definite diagnosis (    <xref ref-type="bibr" rid="ref10">10</xref>
). Metastatic colon carcinoma shows CK20 positivity and CK7 negativity in contrast to the adjacent bile duct epithelium, which is CK7-positive and CK20- negative (    <xref ref-type="bibr" rid="ref11">11</xref>
). In our case, no CK7 expression was found. According to the result, metastatic adenocarcinoma would be considered first rather than primary biliary duct malignancy. In our case, imaging studies revealed obstructive jaundice without an intraparenchymal mass. Biopsy techniques for intrabiliary lesions include brush cytology, clamshell forceps under choledochoscopic guidance, and clamshell forceps under fluoroscopic guidance. In a previous study, the choledochoscope-directed biopsy technique had highest sensitivity and specificity, but this difference was not statistically significant (    <xref ref-type="bibr" rid="ref12">12</xref>
). However, in this study, the patient refused to accept endoscopic retrograde cholangiopancreatography (ERCP), and clamshell forceps were not available in our hospital; thus, we performed transhepatic biopsy. Because ductal thickening with soft tissue density cannot be well identified under sonography, real-time USG combined with CT is useful for localizing inconspicuous focal hepatic lesions (    <xref ref-type="bibr" rid="ref13">13</xref>
). The etiology of intrabiliary growth of liver metastasis is unknown, but the etiology probably involves vascular invasion or the implantation of malignant cells in the biliary epithelium through bile flow (    <xref ref-type="bibr" rid="ref14">14</xref>
). Patients with intrabiliary metastasis have better prognosis than patients without metastasis; moreover, patients with macroscopic involvement have a much higher 5-year survival rate (80%) than those with microscopic involvement (    <xref ref-type="bibr" rid="ref15">15</xref>
). However, the condition of our patient was poor, his total bilirubin levels increased again, and his liver function worsened, even after two PTCDs were inserted on both sides; consequently, the patient was transferred to the hospice ward and died 1 month later.</p>
  </sec>
  <sec id="sec-4">
   <title>Conclusion</title>
   <p id="b-5">In conclusion, intrabiliary metastasis is easily overlooked. An immunohistochemical study is helpful to achieve the correct diagnosis and management.</p>
  </sec>
 </body>
 <back>
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