<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD Journal Publishing DTD v2.3 20070202//EN" "journalpublishing.dtd">
<?xml-stylesheet type="text/xsl" href="ViewNLM-v2.3.xsl"?>
<article xml:lang="KO" article-type="case-report">

<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">J Korean Surg Soc</journal-id>
<journal-id journal-id-type="publisher-id">JKSS</journal-id>
<journal-title>Journal of the Korean Surgical Society</journal-title>
<issn pub-type="ppub">1226-0053</issn>
<issn pub-type="epub">2093-0488</issn>
<publisher>
<publisher-name>The Korean Surgical Society</publisher-name>
</publisher>
</journal-meta>

<article-meta>

<article-id pub-id-type="doi">10.4174/jkss.2010.79.Suppl1.S62</article-id>

<article-categories>
<subj-group>
<subject>Case Report</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Infantile Fibrosarcoma in Neonate</article-title>
</title-group>

<contrib-group>

<contrib contrib-type="author">
<name>
<surname>Nam</surname>
<given-names>So-Hyun</given-names>
</name>
<degrees>M.D.</degrees>
<xref ref-type="aff" rid="A1"></xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname>Cho</surname>
<given-names>Min-Jung</given-names>
</name>
<degrees>M.D.</degrees>
<xref ref-type="aff" rid="A2">1</xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname>Kim</surname>
<given-names>Dae-Yeon</given-names>
</name>
<degrees>M.D.</degrees>
<xref ref-type="aff" rid="A2">1</xref>
</contrib>

<contrib contrib-type="author" corresp="yes">
<name>
<surname>Kim</surname>
<given-names>Seong-Chul</given-names>
</name>
<degrees>M.D.</degrees>
<xref ref-type="aff" rid="A2">1</xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname>Kim</surname>
<given-names>In-Koo</given-names>
</name>
<degrees>M.D.</degrees>
<xref ref-type="aff" rid="A2">1</xref>
</contrib>

</contrib-group>

<aff id="A1">Department of Surgery, Inje University Haeundae Paik Hospital, Busan, Korea.</aff>
<aff id="A2"><label>1</label>Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.</aff>

<author-notes>
<corresp>Corresponding author (<email>sckim@amc.seoul.kr</email>)</corresp>
</author-notes>

<pub-date pub-type="ppub">
<month>12</month>
<year>2010</year>
</pub-date>
<pub-date pub-type="epub">
<day>31</day>
<month>12</month>
<year>2010</year>
</pub-date>
<volume>79</volume>
<issue>Suppl 1</issue>
<fpage>S62</fpage>
<lpage>S66</lpage>
<history>
<date date-type="received">
<day>16</day>
<month>03</month>
<year>2010</year>
</date>
<date date-type="accepted">
<day>24</day>
<month>05</month>
<year>2010</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2010 The Korean Surgical Society</copyright-statement>
<copyright-year>2010</copyright-year>
</permissions>

<abstract>
<p>Infantile fibrosarcoma is a rare malignant soft tissue tumor occurring especially in newborn and young children under 2 years. We experienced three cases of infantile fibrosarcoma presenting in the neonatal period. Case 1 presented with a multiseptated cystic mass on his left thigh at birth that was diagnosed as lymphangioma. After picibanil injection, we noted the size of the mass doubled and a solid lesion was prominent in the magnetic resonance image. Case 2 was found to have a reddish mass on his lower back mimicking hemangioma. Over 2 weeks, the mass grew rapidly with internal hemorrhaging. Case 3 was noted to have an encircling mass around the splenic flexure, which developed into congenital bowel obstruction. All of the tumors were resected completely, but microscopic resection margin was not clear in two patients. The two patients received adjuvant chemotherapy and all patients are well without evidence of recurrence.</p>
</abstract>

<kwd-group>
<kwd>Infantile fibrosarcoma</kwd>
<kwd>Congenital lymphangioma</kwd>
<kwd>Congenital hemangioma</kwd>
<kwd>Congenital bowel obstruction</kwd>
</kwd-group>

</article-meta>
</front>

<back>

<ref-list>

  <ref id="B1">
    <label>1</label>
    <nlm-citation citation-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Cofer</surname>
          <given-names>BR</given-names>
        </name>
        <name>
          <surname>Vescio</surname>
          <given-names>PJ</given-names>
        </name>
        <name>
          <surname>Wiener</surname>
          <given-names>ES</given-names>
        </name>
      </person-group>
      <article-title>Infantile fibrosarcoma: complete excision is the appropriate treatment</article-title>
      <source>Ann Surg Oncol</source>
      <year>1996</year>
      <volume>3</volume>
      <fpage>159</fpage>
      <lpage>161</lpage>
    </nlm-citation>
  </ref>

  <ref id="B2">
    <label>2</label>
    <nlm-citation citation-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Kurkchubasche</surname>
          <given-names>AG</given-names>
        </name>
        <name>
          <surname>Halvorson</surname>
          <given-names>EG</given-names>
        </name>
        <name>
          <surname>Forman</surname>
          <given-names>EN</given-names>
        </name>
        <name>
          <surname>Terek</surname>
          <given-names>RM</given-names>
        </name>
        <name>
          <surname>Ferguson</surname>
          <given-names>WS</given-names>
        </name>
      </person-group>
      <article-title>The role of preoperative chemotherapy in the treatment of infantile fibrosarcoma</article-title>
      <source>J Pediatr Surg</source>
      <year>2000</year>
      <volume>35</volume>
      <fpage>880</fpage>
      <lpage>883</lpage>
    </nlm-citation>
  </ref>

  <ref id="B3">
    <label>3</label>
    <nlm-citation citation-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Cecchetto</surname>
          <given-names>G</given-names>
        </name>
        <name>
          <surname>Carli</surname>
          <given-names>M</given-names>
        </name>
        <name>
          <surname>Alaggio</surname>
          <given-names>R</given-names>
        </name>
        <name>
          <surname>Dall'Igna</surname>
          <given-names>P</given-names>
        </name>
        <name>
          <surname>Bisogno</surname>
          <given-names>G</given-names>
        </name>
        <name>
          <surname>Scarzello</surname>
          <given-names>G</given-names>
        </name>
        <etal/>
      </person-group>
      <article-title>Fibrosarcoma in pediatric patients: results of the Italian Cooperative Group studies (1979-1995)</article-title>
      <source>J Surg Oncol</source>
      <year>2001</year>
      <volume>78</volume>
      <fpage>225</fpage>
      <lpage>231</lpage>
    </nlm-citation>
  </ref>

  <ref id="B4">
    <label>4</label>
    <nlm-citation citation-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Frieden</surname>
          <given-names>IJ</given-names>
        </name>
        <name>
          <surname>Rogers</surname>
          <given-names>M</given-names>
        </name>
        <name>
          <surname>Garzon</surname>
          <given-names>MC</given-names>
        </name>
      </person-group>
      <article-title>Conditions masquerading as infantile haemangioma: Part 2</article-title>
      <source>Australas J Dermatol</source>
      <year>2009</year>
      <volume>50</volume>
      <fpage>153</fpage>
      <lpage>170</lpage>
    </nlm-citation>
  </ref>

  <ref id="B5">
    <label>5</label>
    <nlm-citation citation-type="book">
      <person-group person-group-type="author">
        <name>
          <surname>Okcu</surname>
          <given-names>MF</given-names>
        </name>
        <name>
          <surname>Hicks</surname>
          <given-names>J</given-names>
        </name>
        <name>
          <surname>Merchant</surname>
          <given-names>TE</given-names>
        </name>
        <name>
          <surname>Andrassy</surname>
          <given-names>RJ</given-names>
        </name>
        <name>
          <surname>Pappo</surname>
          <given-names>AS</given-names>
        </name>
        <name>
          <surname>Horowitz</surname>
          <given-names>ME</given-names>
        </name>
      </person-group>
      <person-group person-group-type="editor">
        <name>
          <surname>Pizzo</surname>
          <given-names>PA</given-names>
        </name>
        <name>
          <surname>Poplack</surname>
          <given-names>DG</given-names>
        </name>
      </person-group>
      <article-title>Nonrhabdomyosarcomatous soft tissue sarcomas</article-title>
      <source>Principles and Practice of Pediatric Oncology</source>
      <year>2006</year>
      <edition>5th ed</edition>
      <publisher-loc>Philadelphia</publisher-loc>
      <publisher-name>Lippincott Williams &#x0026; Wilkins</publisher-name>
      <fpage>1055</fpage>
      <lpage>1059</lpage>
    </nlm-citation>
  </ref>

  <ref id="B6">
    <label>6</label>
    <nlm-citation citation-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Asgari</surname>
          <given-names>M</given-names>
        </name>
        <name>
          <surname>Rubin</surname>
          <given-names>BP</given-names>
        </name>
        <name>
          <surname>Hornung</surname>
          <given-names>RL</given-names>
        </name>
      </person-group>
      <article-title>Neonate with a fibrosarcoma and consumptive coagulopathy</article-title>
      <source>J Am Acad Dermatol</source>
      <year>2004</year>
      <volume>50</volume>
      <fpage>S23</fpage>
      <lpage>S25</lpage>
    </nlm-citation>
  </ref>

  <ref id="B7">
    <label>7</label>
    <nlm-citation citation-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Ramphal</surname>
          <given-names>R</given-names>
        </name>
        <name>
          <surname>Manson</surname>
          <given-names>D</given-names>
        </name>
        <name>
          <surname>Viero</surname>
          <given-names>S</given-names>
        </name>
        <name>
          <surname>Zielenska</surname>
          <given-names>M</given-names>
        </name>
        <name>
          <surname>Gerstle</surname>
          <given-names>T</given-names>
        </name>
        <name>
          <surname>Pappo</surname>
          <given-names>A</given-names>
        </name>
      </person-group>
      <article-title>Retroperitoneal infantile fibrosarcoma: clinical, molecular, and therapeutic aspects of an unusual tumor</article-title>
      <source>Pediatr Hematol Oncol</source>
      <year>2003</year>
      <volume>20</volume>
      <fpage>635</fpage>
      <lpage>642</lpage>
    </nlm-citation>
  </ref>

  <ref id="B8">
    <label>8</label>
    <nlm-citation citation-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>van Niekerk</surname>
          <given-names>ML</given-names>
        </name>
        <name>
          <surname>Nel</surname>
          <given-names>WA</given-names>
        </name>
        <name>
          <surname>Slavik</surname>
          <given-names>T</given-names>
        </name>
      </person-group>
      <article-title>Infantile fibrosarcoma of the ileum presenting with congenital bowel obstruction</article-title>
      <source>J Pediatr Surg</source>
      <year>2010</year>
      <volume>45</volume>
      <fpage>461</fpage>
      <lpage>462</lpage>
    </nlm-citation>
  </ref>

  <ref id="B9">
    <label>9</label>
    <nlm-citation citation-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Orbach</surname>
          <given-names>D</given-names>
        </name>
        <name>
          <surname>Rey</surname>
          <given-names>A</given-names>
        </name>
        <name>
          <surname>Cecchetto</surname>
          <given-names>G</given-names>
        </name>
        <name>
          <surname>Oberlin</surname>
          <given-names>O</given-names>
        </name>
        <name>
          <surname>Casanova</surname>
          <given-names>M</given-names>
        </name>
        <name>
          <surname>Thebaud</surname>
          <given-names>E</given-names>
        </name>
        <etal/>
      </person-group>
      <article-title>Infantile fibrosarcoma: management based on the European experience</article-title>
      <source>J Clin Oncol</source>
      <year>2010</year>
      <volume>28</volume>
      <fpage>318</fpage>
      <lpage>323</lpage>
    </nlm-citation>
  </ref>

  <ref id="B10">
    <label>10</label>
    <nlm-citation citation-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Shetty</surname>
          <given-names>AK</given-names>
        </name>
        <name>
          <surname>Yu</surname>
          <given-names>LC</given-names>
        </name>
        <name>
          <surname>Gardner</surname>
          <given-names>RV</given-names>
        </name>
        <name>
          <surname>Warrier</surname>
          <given-names>RP</given-names>
        </name>
      </person-group>
      <article-title>Role of chemotherapy in the treatment of infantile fibrosarcoma</article-title>
      <source>Med Pediatr Oncol</source>
      <year>1999</year>
      <volume>33</volume>
      <fpage>425</fpage>
      <lpage>427</lpage>
    </nlm-citation>
  </ref>

</ref-list>

</back>

<floats-wrap>

<fig position="float" id="F1">
<label>Fig. 1</label>
<caption>
  <p>(A) Ultrasonography shows multiseptated cystic mass with internal hemorrhage on the left thigh. (B) Coronal T2 weighted MR image reveals a huge mass with remarkable solid portion and lesional heterogeneity. (C) Cut surface appearance of gross specimen shows grayish white solid mass with internal hemorrhage and necrosis. (D) Microscopic examination shows herringbone pattern of spindled fibrosarcoma cell with high cellularity and mitosis (H&#x0026;E stain, &#x00D7;400).</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="jkss-79-S62-g001" alt-version="no"></graphic>
</fig>

<fig position="float" id="F2">
<label>Fig. 2</label>
<caption>
  <p>(A) Sagittal T2 weighted MR image reveals a hyperintense homogenous, well defined mass on the back without connection to spinal canal. (B) The exophytic hard mass is rapidly growing with the overlying skin stretching with ulceration.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="jkss-79-S62-g002" alt-version="no"></graphic>
</fig>

<fig position="float" id="F3">
<label>Fig. 3</label>
<caption>
  <p>Abdominal CT scan shows a 3.5 cm hyperdense mass at the splenic flexure, which developed bowel obstruction.</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="jkss-79-S62-g003" alt-version="no"></graphic>
</fig>

</floats-wrap>

</article>