A Case of Paroxysmal Nocturnal Hemoglobinuria

발작성야간혈색소뇨증 1례

  • Kim, Chung-Sook (Department of Clinical Pathology, College of Medicine, Yeungnam University) ;
  • Kim, Kyung-Dong (Department of Clinical Pathology, College of Medicine, Yeungnam University) ;
  • Lee, Heon-Ju (Department of Internal Medicine, College of Medicine, Yeungnam University)
  • 김정숙 (영남대학교 의과대학 임상병리학교실) ;
  • 김경동 (영남대학교 의과대학 임상병리학교실) ;
  • 이헌주 (영남대학교 의과대학 내과학교실)
  • Published : 1989.06.30

Abstract

Paroxysmal nocturnal hemoglobinuria (PNH) is an uncommon hematologic disease characterized by an abnormal sensitivity of blood cells to the lytic action of serum complement. We experienced one case of PNH in Yeungnam University Hospital from May 1983 to May 1989. The patients was followed up without severe complications for 4 years since diagnosis with the only consevating treatments such as washed blood transfusion, adrenal corticosteroids, androgens, folate and iron preparation, intermittently.

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