Young’s procedure for surgical treatment of epistaxis in hereditary hemorrhagic telangiectasia: A case report and literature review

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Francisco Ringler A.
José Zemelman L.
Felipe Cardemil M.
Constanza Valdés P.

Keywords

Hereditary hemorrhagic telangiectasia, Rendu-Osler-Weber syndrome, recurrent epistaxis, nasal closure

Abstract

Hereditary hemorrhagic telangiectasia (HHT) is a multisystemic vascular dysplasia, of autosomal dominant inheritance, characterized by the development of mucocutaneous te- langiectasias and visceral arteriovenous malformations. The diagnosis is made using the Curafao criteria published in 2000 and its management requires a multidisciplinary team where the role of the ENTs is fundamental, since epistaxis occurs in 90%-95% of patients, being one of the first clinical manifestations of the disease and may threaten the life of the patient. Multiple medical and surgical treatment alternatives for epistaxis are described in the literature without a definitive treatment for the disease. Here, we present the case of a 56-year-old patient with severe recurrent HHT and epistaxis who, after not responding to the initial conservative and surgical treatments, a nasal closure was performed, using the Young’s procedure, constituting the first case reported in our country.

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