<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.1 20151215//EN" "JATS-journalpublishing1.dtd">
<article xml:lang="EN" article-type="case-report">

<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Investig Magn Reson Imaging</journal-id>
<journal-id journal-id-type="publisher-id">IMRI</journal-id>
<journal-title-group>
<journal-title>Investigative Magnetic Resonance Imaging</journal-title>
</journal-title-group>
<issn pub-type="ppub">2384-1095</issn>
<issn pub-type="epub">2384-1109</issn>
<publisher>
<publisher-name>Korean Society of Magnetic Resonance in Medicine</publisher-name>
</publisher>
</journal-meta>

<article-meta>
<article-id pub-id-type="doi">10.13104/imri.2015.19.4.237</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Case Report</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Invasive Ductal Carcinoma Arising within a Mammary Hamartoma: Case Report</article-title>
</title-group>

<contrib-group>

<contrib contrib-type="author">
<name>
<surname>Bae</surname>
<given-names>Jung Min</given-names>
</name>
<xref ref-type="aff" rid="A1"></xref>
</contrib>

<contrib contrib-type="author" corresp="yes">
<name>
<surname>Ko</surname>
<given-names>Eun Young</given-names>
</name>
<xref ref-type="aff" rid="A1"></xref>
</contrib>

<contrib contrib-type="author">
<name>
<surname>Han</surname>
<given-names>Boo-Kyung</given-names>
</name>
<xref ref-type="aff" rid="A1"></xref>
</contrib>

</contrib-group>

<aff id="A1">Department of Radiology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.</aff>

<author-notes>
<corresp>Correspondence to: Eun Young Ko, M.D., Ph.D. Department of Radiology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50, Ilwon-dong, Gangnam-gu, Seoul 135-710, Korea. Tel. +82-2-3410-6418, Fax. +82-2-3410-6368, <email>claudel@skku.edu</email></corresp>
</author-notes>

<pub-date pub-type="ppub">
<month>12</month>
<year>2015</year>
</pub-date>
<pub-date pub-type="epub">
<day>31</day>
<month>12</month>
<year>2015</year>
</pub-date>
<volume>19</volume>
<issue>4</issue>
<fpage>237</fpage>
<lpage>240</lpage>

<history>
<date date-type="received">
<day>03</day>
<month>09</month>
<year>2015</year>
</date>
<date date-type="rev-recd">
<day>17</day>
<month>09</month>
<year>2015</year>
</date>
<date date-type="accepted">
<day>19</day>
<month>09</month>
<year>2015</year>
</date>
</history>

<permissions>
<copyright-statement>Copyright &#x00A9; 2015 Korean Society of Magnetic Resonance in Medicine (KSMRM)</copyright-statement>
<copyright-year>2015</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc/3.0/">
<license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (<ext-link ext-link-type="uri" xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://creativecommons.org/licenses/by-nc/3.0/">http://creativecommons.org/licenses/by-nc/3.0/</ext-link>) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>

<abstract>

<p>Breast hamartomas are typically a benign condition and rarely develop into malignant lesions. The coexistence of carcinoma and a breast hamartoma is rare; only 15 cases have been reported in the literature. Here, we report a case of invasive ductal carcinoma associated with hamartoma in a 60-year-old woman. Mammography, ultrasonography and magnetic resonance imaging showed typical features of a breast hamartoma and a suspicious mass with microcalcifications arising within the hamartoma.</p>

</abstract>

<kwd-group>
<kwd>Breast</kwd>
<kwd>Hamartoma</kwd>
<kwd>Invasive carcinoma</kwd>
<kwd>Magnetic resonance imaging</kwd>
</kwd-group>

</article-meta>
</front>

<body>

<sec sec-type="intro">
<title>INTRODUCTION</title>
  <p>Breast hamartomas are uncommon benign breast lesions composed of varying amounts of fatty, fibrous, and glandular elements, and are well-defined or encapsulated, separated from the rest of the glandular tissue (<xref ref-type="bibr" rid="B1">1</xref><xref ref-type="bibr" rid="B2">2</xref>). Hamartomas are not a risk factor for breast cancer development. However, there have been several reports of coexistence of carcinoma associated with hamartoma, suggesting possible malignant transformation of breast hamartomas (<xref ref-type="bibr" rid="B3">3</xref>). In this case report, we present a new incident of invasive ductal carcinoma (IDC) arising in a breast hamartoma.</p>
</sec>

<sec sec-type="cases">
<title>CASE REPORT</title>
  <p>A 60-year-old woman presented with a palpable mass in her right breast. The mass had been present for several decades. One month ago, she received an abnormal result on a screening mammography which was performed at an outside hospital during a regular health check-up. She denied any history of breast surgery, trauma to either breast, or a family history of breast cancer. Physical examination revealed a 10-cm-sized soft, painless, and mobile mass in the right upper breast. Dimpling or retraction was not present. Mammography was performed at our institution and it showed a 10-cm-sized, circumscribed, irregular, fat-containing mass with a surrounding thin pseudocapsule. Within this fatty mass, in the right upper outer quadrant, a 3.5-cm-sized irregular hyperdense mass containing suspicious microcalcifications was also noted (<xref ref-type="fig" rid="F1">Fig. 1a, b</xref>). Using breast ultrasonography (US), a 10-cm-sized circumscribed oval isoechoic mass was detected in the right upper breast, and an additional 3.5-cm-sized irregular hypoechoic mass was noted within the fatty mass (<xref ref-type="fig" rid="F1">Fig. 1c</xref>). Suspecting breast cancer arising from a breast hamartoma, US-guided core needle biopsy using 14 gaze needle was performed, and the hypoechoic mass was proven to be an IDC. Magnetic resonance imaging (MRI) was performed preoperatively and showed a 10 cm, encapsulated fat-containing mass in the right breast suggesting breast hamartoma. And within the hamartoma, 3.5-cm-sized irregular mass with heterogeneous enhancement was noted, suggesting malignancy (<xref ref-type="fig" rid="F1">Fig. 1d-f</xref>). An ipsilateral axillary lymph node was enlarged, suggesting metastasis.</p>

  <p>Right partial mastectomy and sentinel lymph node biopsy was performed. The gross specimen revealed a large hamartoma with a smaller malignant mass which appeared as a poorly-defined, white-tan, solid mass (<xref ref-type="fig" rid="F1">Fig. 1g</xref>). One ipsilateral axillary lymph node was proven to be a metastatic lymph node. The patient underwent postoperative adjuvant chemotherapy and radiation therapy and is under regular follow up observation without tumor recurrence.</p>
</sec>

<sec sec-type="discussion">
<title>DISCUSSION</title>
  <p>Hamartoma of the breast is a rare, benign tumor, with a prevalence of &#x003C; 1% of all breast lesions. The prevalence is generally underestimated because the tumor is often asymptomatic and frequently undiagnosed (<xref ref-type="bibr" rid="B4">4</xref>). On physical examination, hamartoma is usually a well-defined, soft, painless and mobile tumor (<xref ref-type="bibr" rid="B5">5</xref>). Hamartomas are often diagnosed incidentally during a screening mammography on which they show a characteristic appearance consisting of a circumscribed mass with a thin pseudocapsule and mixed fatty and soft-tissue elements (<xref ref-type="bibr" rid="B2">2</xref><xref ref-type="bibr" rid="B6">6</xref>). US features of breast hamartoma are variable, but usually appear as a well-circumscribed, oval-shaped, solid mass with internal heterogeneous echogenicity ('breast within breast appearance'). Sometimes it can be difficult to distinguish a hamartoma from the surrounding breast tissue (<xref ref-type="bibr" rid="B7">7</xref>). MRI shows the presence of internal fat density as well as smooth well defined hypointense rim and internal heterogeneous enhancement, which are characteristic of breast hamartoma (<xref ref-type="bibr" rid="B4">4</xref>).</p>

  <p>According to several papers that reported malignancy associated with breast hamartoma, mammography mostly revealed a spiculated mass or a fatty mass containing suspicious microcalcifications within the hamartoma. On US, an irregular hypoechoic tumor within the hamartoma is the most common finding, but there are also cases with irregular hypoechoic tumors located both within and external to the hamartoma. Microscopically, hamartomas are composed of a combination of epithelial and stromal elements, usually with normal ducts or lobules (<xref ref-type="bibr" rid="B5">5</xref><xref ref-type="bibr" rid="B6">6</xref>). Malignant tumors arising from the hamartoma are known to show large tumor cells arranged in solid clusters with pleomorphic nuclei (<xref ref-type="bibr" rid="B8">8</xref>).</p>

  <p>Breast hamartoma is a tumor that may be underdiagnosed by pathologists because it does not have any cytologic or architectural specificity. It contains all the constituents of normal breast tissue, and because a breast hamartoma is a benign tumor, it is not thought to be associated with breast cancer (<xref ref-type="bibr" rid="B3">3</xref>). Nevertheless, several reports described different types of malignancy including both non-invasive and invasive carcinomas arising in breast hamartomas. The cause of breast cancer arising from a hamartoma can be explained by the histological equivalence of its components to normal breast tissue. Case reports of carcinomas found in hamartomas suggest that malignant cells can exist in all lesions containing breast tissue. Therefore, the presence of a breast hamartoma does not exclude the possibility of breast cancer originating from this benign lesion (<xref ref-type="bibr" rid="B7">7</xref>).</p>

  <p>For any lesion that shows radiologic features atypical for a hamartoma, such as suspicious additional mass with discriminating imaging features from the hamartoma or increase in size of the mass or development of microcalcifications during follow up, the possibility of breast carcinoma developing within hamartoma should be considered and further pathological diagnosis should be performed (<xref ref-type="bibr" rid="B9">9</xref>).</p>

  <p>In conclusion, breast hamartomas are uncommon benign tumors and associated carcinomas occur only rarely. However, due to the possibility of coexistence of carcinoma with a breast hamartoma, we should be prudent and aware of the suspicious features within a hamartoma during the performance and interpretation of imaging studies.</p>
</sec>

</body>

<back>

<ref-list>
  <ref id="B1">
    <label>1</label>
    <element-citation publication-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Baron</surname>
          <given-names>M</given-names>
        </name>
        <name>
          <surname>Ladonne</surname>
          <given-names>JM</given-names>
        </name>
        <name>
          <surname>Gravier</surname>
          <given-names>A</given-names>
        </name>
        <name>
          <surname>Picquenot</surname>
          <given-names>JM</given-names>
        </name>
        <name>
          <surname>Berry</surname>
          <given-names>M</given-names>
        </name>
      </person-group>
      <article-title>Invasive lobular carcinoma in a breast hamartoma</article-title>
      <source>Breast J</source>
      <year>2003</year>
      <volume>9</volume>
      <fpage>246</fpage>
      <lpage>248</lpage>
    </element-citation>
  </ref>

  <ref id="B2">
    <label>2</label>
    <element-citation publication-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Choi</surname>
          <given-names>N</given-names>
        </name>
        <name>
          <surname>Ko</surname>
          <given-names>ES</given-names>
        </name>
      </person-group>
      <article-title>Invasive ductal carcinoma in a mammary hamartoma: case report and review of the literature</article-title>
      <source>Korean J Radiol</source>
      <year>2010</year>
      <volume>11</volume>
      <fpage>687</fpage>
      <lpage>691</lpage>
    </element-citation>
  </ref>

  <ref id="B3">
    <label>3</label>
    <element-citation publication-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Ruiz-Tovar</surname>
          <given-names>J</given-names>
        </name>
        <name>
          <surname>Reguero-Callejas</surname>
          <given-names>ME</given-names>
        </name>
        <name>
          <surname>Alaez</surname>
          <given-names>AB</given-names>
        </name>
        <etal/>
      </person-group>
      <article-title>Infiltrating ductal carcinoma and ductal carcinoma in situ associated with mammary hamartoma</article-title>
      <source>Breast J</source>
      <year>2006</year>
      <volume>12</volume>
      <fpage>368</fpage>
      <lpage>370</lpage>
    </element-citation>
  </ref>

  <ref id="B4">
    <label>4</label>
    <element-citation publication-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Tse</surname>
          <given-names>GM</given-names>
        </name>
        <name>
          <surname>Law</surname>
          <given-names>BK</given-names>
        </name>
        <name>
          <surname>Ma</surname>
          <given-names>TK</given-names>
        </name>
        <etal/>
      </person-group>
      <article-title>Hamartoma of the breast: a clinicopathological review</article-title>
      <source>J Clin Pathol</source>
      <year>2002</year>
      <volume>55</volume>
      <fpage>951</fpage>
      <lpage>954</lpage>
    </element-citation>
  </ref>

  <ref id="B5">
    <label>5</label>
    <element-citation publication-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Kai</surname>
          <given-names>M</given-names>
        </name>
        <name>
          <surname>Tada</surname>
          <given-names>K</given-names>
        </name>
        <name>
          <surname>Tamura</surname>
          <given-names>M</given-names>
        </name>
        <etal/>
      </person-group>
      <article-title>Breast cancer associated with mammary hamartoma</article-title>
      <source>Breast Cancer</source>
      <year>2012</year>
      <volume>19</volume>
      <fpage>183</fpage>
      <lpage>186</lpage>
    </element-citation>
  </ref>

  <ref id="B6">
    <label>6</label>
    <element-citation publication-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Mester</surname>
          <given-names>J</given-names>
        </name>
        <name>
          <surname>Simmons</surname>
          <given-names>RM</given-names>
        </name>
        <name>
          <surname>Vazquez</surname>
          <given-names>MF</given-names>
        </name>
        <name>
          <surname>Rosenblatt</surname>
          <given-names>R</given-names>
        </name>
      </person-group>
      <article-title><italic>In situ</italic> and infiltrating ductal carcinoma arising in a breast hamartoma</article-title>
      <source>AJR Am J Roentgenol</source>
      <year>2000</year>
      <volume>175</volume>
      <fpage>64</fpage>
      <lpage>66</lpage>
    </element-citation>
  </ref>

  <ref id="B7">
    <label>7</label>
    <element-citation publication-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Lambert</surname>
          <given-names>J</given-names>
        </name>
        <name>
          <surname>Jerjir</surname>
          <given-names>N</given-names>
        </name>
        <name>
          <surname>Casselman</surname>
          <given-names>J</given-names>
        </name>
        <name>
          <surname>Steyaert</surname>
          <given-names>L</given-names>
        </name>
      </person-group>
      <article-title>Invasive lobular carcinoma arising in a hamartoma of the breast: a case report</article-title>
      <source>Clin Breast Cancer</source>
      <year>2015</year>
      <volume>15</volume>
      <fpage>e63</fpage>
      <lpage>e66</lpage>
    </element-citation>
  </ref>

  <ref id="B8">
    <label>8</label>
    <element-citation publication-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Anani</surname>
          <given-names>PA</given-names>
        </name>
        <name>
          <surname>Hessler</surname>
          <given-names>C</given-names>
        </name>
      </person-group>
      <article-title>Breast hamartoma with invasive ductal carcinoma. Report of two cases and review of the literature</article-title>
      <source>Pathol Res Pract</source>
      <year>1996</year>
      <volume>192</volume>
      <fpage>1187</fpage>
      <lpage>1194</lpage>
    </element-citation>
  </ref>

  <ref id="B9">
    <label>9</label>
    <element-citation publication-type="journal">
      <person-group person-group-type="author">
        <name>
          <surname>Lee</surname>
          <given-names>EH</given-names>
        </name>
        <name>
          <surname>Wylie</surname>
          <given-names>EJ</given-names>
        </name>
        <name>
          <surname>Bourke</surname>
          <given-names>AG</given-names>
        </name>
        <name>
          <surname>Bastiaan De Boer</surname>
          <given-names>W</given-names>
        </name>
      </person-group>
      <article-title>Invasive ductal carcinoma arising in a breast hamartoma: two case reports and a review of the literature</article-title>
      <source>Clin Radiol</source>
      <year>2003</year>
      <volume>58</volume>
      <fpage>80</fpage>
      <lpage>83</lpage>
    </element-citation>
  </ref>
</ref-list>

</back>

<floats-group>

<fig position="float" id="F1">
<label>Fig. 1</label>
<caption>
  <title>A 60-year-old woman with a palpable lump in right breast. (a) A right mediolateral oblique mammogram shows a 10 cm, circumscribed, fat-containing mass with a surrounding thin pseudocapsule (arrowheads). Within this fatty mass, in the right upper outer quadrant, a 3.5 cm, irregular hyperdense mass (arrow) is noted. (b) A magnification view of a shows a 3.5 cm, irregular hyperdense mass containing suspicious microcalcifications (arrows) within the fatty mass. (c) Ultrasonography shows a 10 cm, circumscribed oval isoechoic mass in the right upper breast, with a 3.5 cm, irregular hypoechoic mass (arrow) within the large isoechoic mass (arrowheads). (d) Axial precontrast enhanced T1-weighted magnetic resonance (MR) image of the right breast shows a 10 cm, circumscribed, fat-containing mass suggesting breast hamartoma (arrowheads). Within the mass, a 3.5 cm, irregular shaped, isointense mass compared with the muscle is also noted (arrow). (e) T2-weighted MR image of the right breast shows heterogeneous high signal intensity of the 3.5 cm mass (arrow). (f) On axial contrast-enhanced T1-weighted MR image, the mass within the hamartoma shows avid heterogeneous enhancement (arrow). (g) Gross specimen shows a 10.5 &#x00D7; 9 &#x00D7; 5 cm hamartoma with a 3.5 &#x00D7; 3.1 &#x00D7; 2.5 cm mass which appears as a poorly-defined, firm, white-tan, solid mass (arrow).</title>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="imri-19-237-g001"></graphic>
</fig>

</floats-group>

</article>