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<article article-type="research-article" dtd-version="1.3" xml:lang="en">
  <front>
    <journal-meta>
      <journal-title-group>
        <journal-title>Czech and Slovak Ophthalmology</journal-title>
      </journal-title-group>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">97</article-id>
      <article-id pub-id-type="doi">10.31348/2018/5/6</article-id>
      <article-categories>
        <subj-group>
          <subject>Case report</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Pachychoroid Disease of the Macula – Case Report</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Stěpanov</surname>
            <given-names>Alexandr</given-names>
          </name>
          <contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-8462-8756</contrib-id>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Studnička</surname>
            <given-names>Jan</given-names>
          </name>
          <contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-9911-4379</contrib-id>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Jirásková</surname>
            <given-names>Naďa</given-names>
          </name>
        </contrib>
      </contrib-group>
      <pub-date date-type="pub" publication-format="electronic">
        <day>27</day>
        <month>3</month>
        <year>2019</year>
      </pub-date>
      <issue>5</issue>
      <elocation-id>6</elocation-id>
      <abstract>
        <p>Pachychoroid disease of the macula includes four stages: pachychoroid pigment epitelopathy, central serous chorioretinopathy, pachychoroid neovasculopathy, and polypoid choroidal vasculopathy. Their basic common features are increase in choroidal thickness ≥ 300 μm, pathologically dilated choroidal vessels in the Haller’s layer with thinning of Sattle's layer and choriocapillaris layer. We report the case of a woman at the age of sixty-one, in which we have monitored the complete development of this disease within 8 years.</p>
      </abstract>
      <kwd-group>
        <kwd>pachychoroid disease of the macula</kwd>
        <kwd>choroidal neovascular membrane</kwd>
        <kwd>choroid</kwd>
        <kwd>EDI-OCT</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <back>
    <ref-list>
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  </back>
</article>
