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  <title>Repository Collection: null</title>
  <link rel="alternate" href="https://kumel.medlib.dsmc.or.kr/handle/2015.oak/826" />
  <subtitle />
  <id>https://kumel.medlib.dsmc.or.kr/handle/2015.oak/826</id>
  <updated>2026-04-04T15:32:48Z</updated>
  <dc:date>2026-04-04T15:32:48Z</dc:date>
  <entry>
    <title>Supravalvar Aortic Stenosis 1례</title>
    <link rel="alternate" href="https://kumel.medlib.dsmc.or.kr/handle/2015.oak/14506" />
    <author>
      <name>권태찬</name>
    </author>
    <author>
      <name>김성호</name>
    </author>
    <author>
      <name>강진무</name>
    </author>
    <id>https://kumel.medlib.dsmc.or.kr/handle/2015.oak/14506</id>
    <updated>2023-01-26T18:02:10Z</updated>
    <published>1986-12-31T15:00:00Z</published>
    <summary type="text">Title: Supravalvar Aortic Stenosis 1례
Author(s): 권태찬; 김성호; 강진무
Abstract: Williams syndrome is an uncommon congenital anomaly which is composed of supravalvar aortic stenosis, peculiar face (elfin facies) and mental retardation. Authors experienced a case of Williams syndrome in a 7 year old girl who had a peculiar face and mental retardation. Diagnosis of supravalvar aortic stenosis was established by catheterization and angiocardiography and aided by EKG and 2-D echocardiography. Aortic stenosis was corrected by surgery and discharged in a good condition. A brief review of the literature was made.</summary>
    <dc:date>1986-12-31T15:00:00Z</dc:date>
  </entry>
  <entry>
    <title>활동성 난관 결핵과 동반된 원발성 난관암 1례</title>
    <link rel="alternate" href="https://kumel.medlib.dsmc.or.kr/handle/2015.oak/14505" />
    <author>
      <name>이두룡</name>
    </author>
    <author>
      <name>육상수</name>
    </author>
    <id>https://kumel.medlib.dsmc.or.kr/handle/2015.oak/14505</id>
    <updated>2023-01-26T18:02:09Z</updated>
    <published>1986-12-31T15:00:00Z</published>
    <summary type="text">Title: 활동성 난관 결핵과 동반된 원발성 난관암 1례
Author(s): 이두룡; 육상수
Abstract: Primary tubal malignancy is the rare tumor of the female genital organs. Wo experienced a case of tubal malignancy combined with active tubal tuberculosis. We present this case with brief review of literature.</summary>
    <dc:date>1986-12-31T15:00:00Z</dc:date>
  </entry>
  <entry>
    <title>후복막강에 위치한 거대자궁근종 1례</title>
    <link rel="alternate" href="https://kumel.medlib.dsmc.or.kr/handle/2015.oak/14504" />
    <author>
      <name>이탁</name>
    </author>
    <author>
      <name>차순도</name>
    </author>
    <author>
      <name>김상표</name>
    </author>
    <id>https://kumel.medlib.dsmc.or.kr/handle/2015.oak/14504</id>
    <updated>2023-01-26T18:02:09Z</updated>
    <published>1986-12-31T15:00:00Z</published>
    <summary type="text">Title: 후복막강에 위치한 거대자궁근종 1례
Author(s): 이탁; 차순도; 김상표
Abstract: A Case of giant uterine myoma occupied in retroperitoneum in 48-year old nulliparous womani is presented, and its literatures are reviewed briefly.</summary>
    <dc:date>1986-12-31T15:00:00Z</dc:date>
  </entry>
  <entry>
    <title>비전형적 피부양상을 보인 표피모반의 1례</title>
    <link rel="alternate" href="https://kumel.medlib.dsmc.or.kr/handle/2015.oak/14503" />
    <author>
      <name>김용대</name>
    </author>
    <author>
      <name>김병철</name>
    </author>
    <author>
      <name>이규석</name>
    </author>
    <author>
      <name>송준영</name>
    </author>
    <author>
      <name>이동훈</name>
    </author>
    <id>https://kumel.medlib.dsmc.or.kr/handle/2015.oak/14503</id>
    <updated>2023-01-26T18:02:09Z</updated>
    <published>1986-12-31T15:00:00Z</published>
    <summary type="text">Title: 비전형적 피부양상을 보인 표피모반의 1례
Author(s): 김용대; 김병철; 이규석; 송준영; 이동훈
Abstract: Epidermal nevus is a congenital malformation consisting of wartlike and scaling overgrowth of the epidermis without nevus cell and described by a great terms which denote some distinctive manifestation of the nevus. The authors report a case of verrucous epidermal nevus in a 25-year-old female who had skin colored verrucous gyrate mass on the Rt side of scalp and multiple scattered brownish colored plagues on the Rt side of verrucouse. At the age of 2, the lesion of scalp has become cerebriform appearance. Her growth development and performance within normal range and any abnormalities of the bones ＆ central nervus system were not found. The authors made diagnosis of verrucous epidermal news from characteristic clinical and histopathological findings. Related literature was briefly reviewed for the discussion.</summary>
    <dc:date>1986-12-31T15:00:00Z</dc:date>
  </entry>
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