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hemophilia a/edema
Veza se sprema u međuspremnik
Stranica 1 iz 27 rezultatima
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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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
More on Munchhausen's syndrome in hematology: factitious limb edema in a patient with hemophilia.
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[Suggillation and edema of all extremities (blood coagulation tests and serum reactions): (acquired blood coagulation factor VIII deficiency--hemorrhagic tendency caused by a circulating anticoagulation factor)].
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Clinicopathological features of TAFRO syndrome complicated by acquired hemophilia A and development of cardiopulmonary arrest that were successfully treated with VA-ECMO and tocilizumab.
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TAFRO syndrome and acquired hemophilia A (AHA) are rare, life-threatening diseases; however, the relationship between these two diseases is unknown. A 25-year-old man was transferred to our hospital because of bleeding tendency accompanied by multiple organ failure with generalized edema, massive
Oral Corticosteroid Therapy as an Adjuvant Treatment for Acute Bleeding in Hemophilia Patients With High Titer Inhibitors.
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Treatment options exist for patients with severe hemophilia and high titer factor VIII inhibitors but is often inadequate. Few studies have been conducted to evaluate the utility of short-term corticosteroid therapy for improvement in bleeding complications and temporary or sustained resolution of
Anesthetic management of a patient with hemophilia A with spontaneous acute subdural hematoma.
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Intracranial hemorrhage in patients with hemophilia is associated with high mortality and sequelae. We report the case of 50-year-old man with Hemophilia A, who presented with spontaneous acute subdural hematoma and underwent craniotomy for clot evacuation. The patient received Factor VIII infusions
Comorbidity of constrictive pericarditis and hemophilia A.
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OBJECTIVE
To report a case of comorbidity of constrictive pericarditis and hemophilia A.
METHODS
A 21-year-old male with hemophilia A was referred to our clinic and was examined with the subsequent evaluation of shortness of breath, leg edema and ascites. Clinical and laboratory examinations were
[Comparison of radiography and magnetic resonance imaging in detecting arthropathies in patients with hemophilia].
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OBJECTIVE
To compare magnetic resonance imaging (MRI) and radiography in detecting arthropathies in patients with hemophilia.
METHODS
Of 41 symptomatic joint images in the 14 patients with hemophilia, each joint was examined with both radiography and MRI within the same day. Imaging findings with
Nephrotic syndrome associated with hypocomplementemia in a 4-year-old boy with hemophilia B.
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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
Efficacy, Safety, and Pharmacokinetics of Beroctocog Alfa in Patients Previously Treated for Hemophilia A.
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OBJECTIVE
Beroctocog alfa is a second generation recombinant factor VIII manufactured by removing the B-domain from factor VIII. This prospective clinical trial was conducted to evaluate the efficacy, safety, and pharmacokinetics of beroctocog alfa in patients of ages ≥12 years previously treated
Hemobilia after liver biopsy. Early detection in a patient with mild hemophilia A.
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Hemobilia occurred following liver biopsy in a patient with mild hemophilia A, despite adequate factor VIII transfusion. Before major hemorrhage occurred, the diagnosis of hemobilia was confirmed by endoscopy and retrograde cholangiography. Two aneurysms of the hepatic artery were found in the
A case of concurrent proteus syndrome and hemophilia a.
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BACKGROUND
Proteus syndrome is a very rare condition with less than 100 confirmed cases reported worldwide. We report a case of Proteus syndrome in a two-year-old male who has hemophilia A comorbidity.
METHODS
A two-year-old male patient was admitted with the chief complaint of severe bleeding in
Gradual deterioration of brainstem cavernous angioma associated with hemophilia--case report.
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A 49-year-old man presented with a brainstem cavernous angioma associated with hemophilia manifesting as gradual progression of neurological deficits over a period of 2 weeks. Computed tomography revealed a hematoma and perifocal edema on the left side of the pons, and T(2)-weighted magnetic
Circumcision in hemophilia: a cost-effective method using a novel device.
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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;
[Acquired hemophilia A developed at relapse of minimal change nephrotic syndrome].
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We present a case of a 74-year-old male, who had a relapse of minimal change nephrotic syndrome (MCNS) as the initial presentation of acquired hemophilia A. MCNS had been maintained in remission with prednisolone 10 mg for 15 years. In early December 2005, the patient developed edema of the right
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