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  <title>Repository Collection: null</title>
  <link rel="alternate" href="https://kumel.medlib.dsmc.or.kr/handle/2015.oak/842" />
  <subtitle />
  <id>https://kumel.medlib.dsmc.or.kr/handle/2015.oak/842</id>
  <updated>2026-04-04T17:01:51Z</updated>
  <dc:date>2026-04-04T17:01:51Z</dc:date>
  <entry>
    <title>이개 및 경부에 발생한 모기질종 2례</title>
    <link rel="alternate" href="https://kumel.medlib.dsmc.or.kr/handle/2015.oak/15954" />
    <author>
      <name>남성일</name>
    </author>
    <author>
      <name>신승진</name>
    </author>
    <author>
      <name>이상윤</name>
    </author>
    <author>
      <name>김중강</name>
    </author>
    <id>https://kumel.medlib.dsmc.or.kr/handle/2015.oak/15954</id>
    <updated>2023-01-26T18:12:08Z</updated>
    <published>2002-12-31T15:00:00Z</published>
    <summary type="text">Title: 이개 및 경부에 발생한 모기질종 2례
Author(s): 남성일; 신승진; 이상윤; 김중강
Abstract: Pilomatricoma is a benign &#xD;
skin tumor originated from hair follicle shich outbreaks commonly in any age group. It is more common in infancy and childhood, mainly involving the head, neck and upper extremities as a solitary mass and showing characteristic gradual growth for the period of a few months to a few years. At Dongsan Medical Center, we have experienced two cases of pilomatricoma through pathological diagnosis after removing the tumors in the posterior auricle and submandibular area. Case 1 was a 3 year-old girl who presented a firm tender mass about 2.5 &amp;times; 2.0 cm in size at the right posterior auricle, and case 2 was a 22 year-old woman who had a firm non-tender mass about 3.0 &amp;times; 3.0 cm in size at the right submandibular area. Both tumors were solitary nodular and well demarkated from subcutaneous tissue. Both patients underwent excision of the masses under general anesthesia. The tumors showed basaloid cells and ghost cells microscopically and diagnosed as pilomatricoma.</summary>
    <dc:date>2002-12-31T15:00:00Z</dc:date>
  </entry>
  <entry>
    <title>비중격에 발생한 다형선종 1례</title>
    <link rel="alternate" href="https://kumel.medlib.dsmc.or.kr/handle/2015.oak/15953" />
    <author>
      <name>안병훈</name>
    </author>
    <author>
      <name>최종원</name>
    </author>
    <author>
      <name>박연호</name>
    </author>
    <author>
      <name>김동은</name>
    </author>
    <author>
      <name>김은덕</name>
    </author>
    <id>https://kumel.medlib.dsmc.or.kr/handle/2015.oak/15953</id>
    <updated>2023-01-26T18:12:07Z</updated>
    <published>2002-12-31T15:00:00Z</published>
    <summary type="text">Title: 비중격에 발생한 다형선종 1례
Author(s): 안병훈; 최종원; 박연호; 김동은; 김은덕
Abstract: Pleomorphic adenoma is a &#xD;
kind of salivary gland neoplasm and is derived from the epithelial and mesenchymal elements. It is rarely found in the upper respiratory tract, especially in the nasal cavity. We experienced a case of pleomorphic adenoma arising from the nasal septum, and present herein the case with the review of literatures.</summary>
    <dc:date>2002-12-31T15:00:00Z</dc:date>
  </entry>
  <entry>
    <title>두경부에 발생한 Castleman병 2례</title>
    <link rel="alternate" href="https://kumel.medlib.dsmc.or.kr/handle/2015.oak/15952" />
    <author>
      <name>송달원</name>
    </author>
    <id>https://kumel.medlib.dsmc.or.kr/handle/2015.oak/15952</id>
    <updated>2023-01-26T18:12:07Z</updated>
    <published>2002-12-31T15:00:00Z</published>
    <summary type="text">Title: 두경부에 발생한 Castleman병 2례
Author(s): 송달원
Abstract: Castleman&amp;#39;s disease is &#xD;
histologically a kind of atypical lymph op roliferative disorders of unknown cause, characterized by massive proliferation of lymphoid tissue. Two histologic variations (hyaline-vaseular and plasma cell) and two clinical types (localized and multicentric) have been described. The author experienced 2 cases of Castleman&amp;#39;s disease (hyaline-vascular, plasma cell). The first case was a 52 year-old female presented with a single lateral neck mass which was diagnosed as hyaline- vascular type by excisional biopsy. The second case was a 54 year-old male presented with both cervical, both axillary and left inguinal lymphadenopathy. The diagnosis of plasma cell type was confirmed by excisional biopsy of the right axillary nodes. The author reports herein the above two cases along with a review of pertinent literature.</summary>
    <dc:date>2002-12-31T15:00:00Z</dc:date>
  </entry>
  <entry>
    <title>부갑상선 선종과 증식증의 수술적 치료</title>
    <link rel="alternate" href="https://kumel.medlib.dsmc.or.kr/handle/2015.oak/15951" />
    <author>
      <name>송달원</name>
    </author>
    <id>https://kumel.medlib.dsmc.or.kr/handle/2015.oak/15951</id>
    <updated>2023-01-26T18:12:07Z</updated>
    <published>2002-12-31T15:00:00Z</published>
    <summary type="text">Title: 부갑상선 선종과 증식증의 수술적 치료
Author(s): 송달원
Abstract: Hyperparathyroidism is commonly seen in adenoma and hyperplasia, and is classified into primary, secondary and tertiary. However, its etiology, pathogenesis, clinical feature and treatment differ from each another. Most primary hyperparathyroidism can be treated by surgical procedures, and the secondary and tertiary hyperparathyroidism can be treated with medication, However, surgical procedures are necessary, if the symptoms persist after taking appropriate medication. This study was undertaken to review the surgical management and postoperative clinical course of three cases of primary and one case of tertiary hyperparathyroidism. Many different preoperative symptoms such as ureteral stone, osteoporosis, gait disturbance and pathologic features were noted during the course of study. Among the imagine studies conducted to localize parathyroid mass, the authors found the parathyroid scan to be most accurate. All four cases underwent surgery which involved removal of only adenoma in two adenoma casesm removal of only enlarged parathyroid gland in one case of hyperplasia with no postoperative, evidence of recurrence, and total parathyroidectomy with autotransplantation in one case of hyperplasia. The hypocalcemia was noted in all four cases after the surgery. Of these four cases, two recovered slowly from hypocalcemia, and one recovered with no symptom of hypocalcemia, but had to take oral calcium and vitamin D for low calcium level. Finally one case with tertiary hyperparathyroidism developed hypocalcemia postoperatively due to chronic renal failure and died of heart failure.</summary>
    <dc:date>2002-12-31T15:00:00Z</dc:date>
  </entry>
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