공동을 동반한 만성 진행성 폐렴양 병변

Chronic Progressive Pneumonic Consolidation with Cavity

  • 권선옥 (연세대학교 의과대학 내과학교실) ;
  • 김형중 (연세대학교 의과대학 내과학교실) ;
  • 안철민 (연세대학교 의과대학 내과학교실) ;
  • 김성규 (연세대학교 의과대학 내과학교실) ;
  • 이원영 (연세대학교 의과대학 내과학교실) ;
  • 김상진 (연세대학교 의과대학 방사선과학교실) ;
  • 이기범 (아주대학교 의과대학 병리학교실)
  • Kwon, Seon-Og (Department of Internal Medicine, Yonsei University College of Medicine) ;
  • Kim, Hyung-Jung (Department of Internal Medicine, Yonsei University College of Medicine) ;
  • Ahn, Chul-Min (Department of Internal Medicine, Yonsei University College of Medicine) ;
  • Kim, Sung-Kyu (Department of Internal Medicine, Yonsei University College of Medicine) ;
  • Lee, Won-Young (Department of Internal Medicine, Yonsei University College of Medicine) ;
  • Kim, Sang-Jin (Department of Riadiology, Yonsei University College of Medicine) ;
  • Lee, Ki-Bum (Department of Pathology, Ajou University, College of Medicine)
  • 발행 : 1991.12.31

초록

Bronchioloalveolar cell carcinoma accounts for less than 6% of all primary lung cancer but has distinct clinical and radiological features and unusual pathologic appearance. The characteristic features are its peripheral location and tendency of rapid progression to diffuse type via aeroginous and lymphatic route without surgical intervention. Among them, mucin secretory type bronchioloalveolar cell carcinoma is the rarest and most distinctive. We experienced a case of mucin secretory type bronchioloalveolar cell carcinoma in a 47 year old female with roentgenographic findings of chronic progressive pulmonary consolidation with muliple cavities.

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