A Case of Mediastinal Cystic Lymphangioma

종격동 낭포성 임파관종 1예

  • Yeo, Dong-Seung (Department of Internal Medicine, College of Medicine, Pusan National University) ;
  • Lee, Dong-Il (Department of Internal Medicine, College of Medicine, Pusan National University) ;
  • Lee, Kwang-Uk (Department of Internal Medicine, College of Medicine, Pusan National University) ;
  • Kang, Dae-Hwan (Department of Internal Medicine, College of Medicine, Pusan National University) ;
  • Park, Soon-Kew (Department of Internal Medicine, College of Medicine, Pusan National University) ;
  • Shin, Young-Kee (Department of Internal Medicine, College of Medicine, Pusan National University)
  • 여동승 (부산대학교 의과대학 내과학교실) ;
  • 이동일 (부산대학교 의과대학 내과학교실) ;
  • 이광욱 (부산대학교 의과대학 내과학교실) ;
  • 강대환 (부산대학교 의과대학 내과학교실) ;
  • 박순규 (부산대학교 의과대학 내과학교실) ;
  • 신영기 (부산대학교 의과대학 내과학교실)
  • Published : 1992.08.31

Abstract

Lymphangiomas are rare benign shlow-growing tumors composed of lymphatic channels. They are generally classified according to the size of their lymph channels as simple, cavernous, and cystic lymphangioma or cystic hygroma. The simple and cavernous types usually occur in the head, neck or axillae. About 75 percent of cystic lymphangioma occur in the neck and 20 percent in the axillae, the remaining 5 percent occur in the mediastinum, omentum, pelvis, groin, spleen, bone, and skin, etc. Purely mediastinal cystic lymphangiomas are very uncommon. We report a case of purely mediastinal cystic lymphangioma confirmed pathologically and treated by operation, along with a review of the literature.

저자들은 매우 드문 것으로 알려진 순수하게 종격동에서 발생한 낭포성 임파관종 1예를 경험하였기에 문헌고찰과 함께 보고하는 바이다.

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