Background: Recurrent epistaxis is the most common manifestation of hereditary hemorrhagic telangiectasia (HHT). The aim of this study was to determine the role and efficacy of argon plasma coagulation (APC) in the management of epistaxis caused by HHT. Methods: From 1997 to 20 04, 43 patients with diagnosed HHT were treated for recurrent epistaxis with APC in our department. Results: Thirty-six patients reported substantial reduction of bleeding after treatment. Of the 18 patients who previously needed blood transfusions, 13 reported substantial reduction of bleeding after treatment and no blood transfusions were necessary. Conclusion: APC allows a control of epistaxis in HHT patients and guarantees a long time free from blood tra...
Hereditary hemorrhagic telangiectasia (HHT: OMIM 187300 and 600376) is an autosomal dominant vascula...
11 p.-6 fig.Epistaxis is the most prevalent clinical symptom in Hereditary Haemorrhagic Telangiectas...
International audienceHereditary hemorrhagic telangiectasia is a rare vascular genetic disease. Epis...
Background: Recurrent epistaxis is the most common manifestation of hereditary hemorrhagic telangiec...
In contrast to the current trend according to which the treatment of hereditary hemorrhagic telangie...
Background: Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant hereditary disorder...
Hereditary hemorrhagic telangiectasia is a rare multi-systemic autosomal dominant disorder character...
Hereditary hemorrhagic telangiectasia is a rare multi-systemic autosomal dominant disorder character...
Hereditary haemorrhagic telangiectasia is a genetic disease that leads to multiregional angiodysplas...
Summary: Epistaxis is a common complication in patients with hereditary hemorrhagic telangiectasia. ...
Hereditary hemorrhagic telangiectasia (HHT), or Rendu-Osler-Weber syndrome, is characterized by tela...
Abstract Patients with Hereditary Hemorrhagic Telangiectasia (HHT) frequently present ...
Abstract Background Epistaxis is the most common symp...
Subjects with the rare autosomal dominant disease Hereditary Hemorrhagic Telangiectasia (HHT) may de...
Abstract Background Severe epistaxis is often difficult to control in patients with hereditary hemor...
Hereditary hemorrhagic telangiectasia (HHT: OMIM 187300 and 600376) is an autosomal dominant vascula...
11 p.-6 fig.Epistaxis is the most prevalent clinical symptom in Hereditary Haemorrhagic Telangiectas...
International audienceHereditary hemorrhagic telangiectasia is a rare vascular genetic disease. Epis...
Background: Recurrent epistaxis is the most common manifestation of hereditary hemorrhagic telangiec...
In contrast to the current trend according to which the treatment of hereditary hemorrhagic telangie...
Background: Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant hereditary disorder...
Hereditary hemorrhagic telangiectasia is a rare multi-systemic autosomal dominant disorder character...
Hereditary hemorrhagic telangiectasia is a rare multi-systemic autosomal dominant disorder character...
Hereditary haemorrhagic telangiectasia is a genetic disease that leads to multiregional angiodysplas...
Summary: Epistaxis is a common complication in patients with hereditary hemorrhagic telangiectasia. ...
Hereditary hemorrhagic telangiectasia (HHT), or Rendu-Osler-Weber syndrome, is characterized by tela...
Abstract Patients with Hereditary Hemorrhagic Telangiectasia (HHT) frequently present ...
Abstract Background Epistaxis is the most common symp...
Subjects with the rare autosomal dominant disease Hereditary Hemorrhagic Telangiectasia (HHT) may de...
Abstract Background Severe epistaxis is often difficult to control in patients with hereditary hemor...
Hereditary hemorrhagic telangiectasia (HHT: OMIM 187300 and 600376) is an autosomal dominant vascula...
11 p.-6 fig.Epistaxis is the most prevalent clinical symptom in Hereditary Haemorrhagic Telangiectas...
International audienceHereditary hemorrhagic telangiectasia is a rare vascular genetic disease. Epis...