Renal failure in paroxysmal nocturnal hemoglobinuria
Hida, M.; Watanabe, J.; Takamiya, T.; Tanaka, K.; Kitamura, M.; Iida, T.; Hiraga, S.; Satoh, T.
Nihon Jinzo Gakkai Shi 31(8): 891-895
1989
ISSN/ISBN: 0385-2385 PMID: 2593321 Document Number: 329227
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, acquired hemolytic disorder characterized by a membrane abnormality of red cells, and characterized by two major clinical features of gross hemoglobinuria and diffuse venous thrombosis. In Japan, the present report records the first case of acute renal failure complicating PNH with treated by hemodialysis and was almost completely reversible. A 41 year-old woman was admitted for high fever (39.8 degrees C), dyspnea and clinical signs of a respiratory infection. She was started on Cefotax 1,000 mg 3 times daily. She subsequently developed acute renal failure and which treated by hemodialysis and was almost completely reversible. Following treatment of her renal failure, respiratory infection and anemia, she initially made good progress and was discharged.