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Danazol for paroxysmal nocturnal hemoglobinuria.

作者信息

Harrington W J, Kolodny L, Horstman L L, Jy W, Ahn Y S

机构信息

Department of Medicine, University of Miami School of Medicine, Florida 33101, USA.

出版信息

Am J Hematol. 1997 Feb;54(2):149-54. doi: 10.1002/(sici)1096-8652(199702)54:2<149::aid-ajh9>3.0.co;2-x.

Abstract

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare clonal stem-cell disorder in which blood cells lack complement inhibiting membrane proteins, and become susceptible to complement-mediated injury, leading to chronic intravascular hemolysis and pancytopenia. Glucocorticoids have been a mainstay of therapy. For patients refractory to glucocorticoids and requiring blood transfusions, an alternative therapy is needed. We studied danazol therapy in 5 patients refractory to other treatments. Four of the 5 benefited, showing rise in hematocrit and eventual cessation of transfusion requirements. Remissions lasted > or =2 years in 3 and 10 years in 1 patient. Danazol was well-tolerated without serious side effects. Danazol appears to be a good alternative treatment in PNH.

摘要

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