Author/Authors
Kızılyel, Okan Atatürk Üniversitesi - Tıp Fakültesi - Deri ve Zührevi Hastalıkları Anabilim Dalı, Turkey , Metin, Mahmut Sami Atatürk Üniversitesi - Tıp Fakültesi - Deri ve Zührevi Hastalıkları Anabilim Dalı, Turkey , Elmas, Ömer Faruk Atatürk Üniversitesi - Tıp Fakültesi - Deri ve Zührevi Hastalıkları Anabilim Dalı, Turkey , Akdeniz, Necmettin Atatürk Üniversitesi - Tıp Fakültesi - Deri ve Zührevi Hastalıkları Anabilim Dalı, Turkey , Karaman, Adem Atatürk Üniversitesi - Tıp Fakültesi - Radyoloji Anabilim Dalı, Turkey
Title Of Article
Osler-Weber-Rendu syndrome: A case report
شماره ركورد
33377
Abstract
Osler-Weber-Rendu (Hereditary Hemorrhagic Telangiectasia) is an autosomal dominant disease characterized by telangiectasia on mucosa and skin and arteriovenous malformations in visceral organs. Telangiectasia on lips, tongue, ear, nasal mucosa, palmoplantar region and nail beds are typical findings in the disease. Visceral arteriovenous malformations are common in patients who have visceral involvements. Our case was 34 years old woman presented with hemangioma on her right side of face and lips, telangiectasia on oral mucosa and arteriovenous malformation in her lower lobe of left lung. Diagnosis was Osler-Weber-Rendu disease. We decided to report this case because it is rarely seen and arteriovenous malformation was present in the lung of the patient.
From Page
119
NaturalLanguageKeyword
Osler , Weber , Rendu syndrome , hereditary hemorrhagic Telangiectasia , pulmonary arteriovenous malformation
JournalTitle
Cumhuriyet Medical Journal
To Page
123
JournalTitle
Cumhuriyet Medical Journal
Link To Document