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hemoglobinuria/ateş

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Sayfa 1 itibaren 119 Sonuçlar

Recurrence of paroxysmal cold hemoglobinuria in a boy after physical cooling for fever.

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Hemolysis and hemoglobinuria after direct exposure to cold has rarely been reported in paroxysmal cold hemoglobinuria (PCH). The authors describe a 2.5-year-old boy with PCH (Donath-Landsteiner autoimmune hemolytic anemia), in whom 16 days after presentation, the hemoglobinuria and hemolysis

[Severe forms of imported malaria concerning three pernicious attacks and a black water fever (hemoglobinuria) (author's transl)].

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Four severe cases of imported malaria are reported here. Three of them are pernicious and the fourth is a black water fever (hemoglobinuria). The difficulties of initial diagnosis are exposed. There was no mortality in these four cases which represent the annual recruiting of a multipurpose

An etiologic study of hemoglobinuria and blackwater fever in the Kivu Mountains, Zaire.

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Between January 1985 and March 1986, in the high altitude area of Kivu, Eastern Zaïre, 38 patients presenting with hemoglobinuria as main manifestation were investigated. Profound glucose-6-phosphate dehydrogenase deficiency was detected in 4 patients, leptospirosis in 2 and Hantaan virus infection

[Typhoid fever complicated by hemoglobinuria; review of literature and case report].

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Hemoglobinuria, blackwater fever, in monkeys; a consideration of the disease in man.

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[Contribution to the study of therapy of bilious fever hemoglobinuria].

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[Two cases of hemoglobinuria bilious fever treated with cortisone].

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[Acute hemolytic reaction (hemoglobinuria fever) in therapy with streptocide].

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[Typhoid fever, hemoglobinuria and glucose-6-phosphate dehydrogenase deficiency. (Apropos of 2 cases)].

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[Analysis of urine in the child without renal disease and with fever].

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The study comprised 24 patients with ages between 5 months and 13 years and fever from different extrarenal infectious diseases. Seventy-nine samples of urine were taken to determine proteins, glucose, ketone, hemoglobine and study of the urinary sediment. Electrophoresis of proteins was practiced
Eculizumab has been developed as a breakthrough treatment for paroxysmal nocturnal hemoglobinuria (PNH). Not only for breakthroughs, eculizumab therapy is also known to increase the risk of invasive meningococcal infection. It has also been recently reported that, although rarely, administration of

[A boy with summer onset paroxysmal cold hemoglobinuria induced by Donath-Landsteiner antibody with anti-I specificity].

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We encountered 4-year-old boy who developed paroxysmal cold hemoglobinuria (PCH) in the middle of August. He was admitted due to progressive jaundice and pallor following fever and nausea. Laboratory data revealed severe anemia, increased serum indirect bilirubin and LDH, and decreased serum

[Hemophagocytosis in a child with paroxysmal cold hemoglobinuria].

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A 2-year and 5-month-old boy was admitted to Okaya municipal hospital because of low grade fever and reddish-brown urine soon after an outside walk in November, 1994. Direct Coombs test was negative, but indirect Coombs test positive. Both sugar water test and Ham test were negative. A diagnosis of

Microvascular thrombosis in the hepatic vein of a patient with paroxysmal nocturnal hemoglobinuria.

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Paroxysmal nocturnal hemoglobinuria (PNH) is characterized by complement-mediated hemolysis, venous thrombosis, and bone marrow failure. In May 2003, a 33-year-old man was admitted to a hospital with right hypochondralgia and fever. He had a history of aplastic anemia. The patient's diagnosis of

Atypical presentation of paroxysmal nocturnal hemoglobinuria treated by eculizumab: A case report.

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Paroxysmal nocturnal hemoglobinuria (PNH) is a nonmalignant acquired hematopoietic stem cell disease, which can be revealed by hemolytic anemia, thromboembolism, or bonemarrow failure. Thrombosis can occur at any site, but coronary thrombosis is extremely rare. Controlled trials have demonstrated
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