hemophilia b/edema

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Anasarca improved by extracorporeal ultrafiltration through an internal shunt in a case of severe haemophilia B with inhibitor and steroid-resistant nephrotic syndrome.

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Prijava / prijava

A patient suffering from severe haemophilia B with factor IX inhibitor developed steroid-resistant nephrotic syndrome. As a result of switching to activated anti-inhibitor coagulant complex (activated prothrombin complex concentrate) agent, FEIBA, bleeding was controlled and internal shunt placement

Nephrotic syndrome associated with hypocomplementemia in a 4-year-old boy with hemophilia B.

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Prijava / prijava

OBJECTIVE The case of a 4-year-old boy with hemophilia B with inhibitor who developed nephrotic syndrome is described. The possible association between factor IX therapy and nephrotic syndrome in patients with hemophilia B is discussed. METHODS A chart review of a 4-year-old boy with hemophilia B

Concurrent lymphoma and hemophilia B in a pediatric patient: A case report.

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Prijava / prijava

Lymphoma is the third most common cancer among children in the United States and Europe. Hemophilia is a congenital bleeding disorder characterized by deficiency of coagulation factor VIII or IX. Hemophilia B is a consequence of factor IX deficiency and has an incidence of 1 in 20,000

[Ultrasonographic characteristics of haemophilic arthropathy in the knee joints].

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Prijava / prijava

OBJECTIVE To investigate the characteristics of ultrasonography in haemophilic arthropathy in knee joints. METHODS The knee joints (n=135) of 68 patients with haemophilia A (n=59) or haemophilia B (n=9) were consecutively evaluated with ultrasonography and scored according to MELCHIORRE ultrasound

Circumcision in hemophilia: a cost-effective method using a novel device.

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Prijava / prijava

OBJECTIVE The authors conducted a prospective clinical study to see whether the need for and the cost of factor substitution after circumcision can be reduced using a novel device for bloodless circumcision in boys with hemophilia. METHODS Forty-five boys with hemophilia (age range, 1.5 to 25 years;

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