Results 1 to 10 of about 1,710,432 (184)

A case of pulmonary arteriovenous malformation in the setting of Rendu Osler Weber syndrome [PDF]

Radiology Case Reports, 2021
Rendu Osler Weber syndrome is a rare disorder, in which arteriovenous malformations are a hallmark feature. We describe the case of a 77-year-old female patient who presented with dyspnea, recurrent epistaxis, and signs of right ventricular heart failure,
Irini Nikolaou, MD, Vasileios Rafailidis, MD, MSc, PhD, EDiR, Anastasios Kartas, MD, MSc, Konstantinos Kouskouras, MD, PhD, George Giannakoulas, MD, PhD   +4 more
doaj   +6 more sources

Life-threatening anaemia in patient with hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber syndrome) [PDF]

Open Medicine, 2020
Hereditary haemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome, is a rare autosomal dominant vascular disorder. Patients with HHT may present with a wide spectrum of clinical manifestations from epistaxis to clinically significant
Mikołajczyk-Solińska Melania, Leończyk Karolina, Brzezina Aleksandra, Rossa Sylwia, Kasznicki Jacek   +4 more
doaj   +4 more sources

Rendu-Osler-Weber Syndrome: case report and literature review [PDF]

Brazilian Journal of Otorhinolaryngology, 2008
Hereditary Hemorrhagic Telangiectasia or Rendu-Osler-Weber Disease is a rare fibrovascular dysplasia that makes vascular walls vulnerable to trauma and rupture, causing skin and mucosa bleeding. It is of dominant autosomal inheritance, characterized by recurrent epistaxis and telangiectasia on the face, hands and oral cavity; visceral arteriovenous ...
Alfredo Rafael Dell'Aringa
exaly   +6 more sources

Rendu-Osler-Weber syndrome: dermatological approach [PDF]

Anais Brasileiros de Dermatologia, 2015
The Rendu-Osler-Weber syndrome is a rare systemic fibrovascular dysplasia, recognized by mucocutaneous telangiectasias, arteriovenous malformations, epistaxis and family history.
Aline Blanco Barbosa, Günter Hans Filho, Carolina Faria dos Santos Vicari, Marcelo Zanolli Medeiros, Daíne Vargas Couto, Luiz Carlos Takita   +5 more
doaj   +7 more sources

Osler‐Weber‐Rendu syndrome: A case report on a rare vascular malformation presented with lower gastrointestinal bleeding

Clinical Case Reports, 2023
Osler‐Weber‐Rendu syndrome is an uncommon vascular disorder inherited as an autosomal dominant trait with varying penetrance and expression. A multidisciplinary approach is used for a detailed diagnostic workup and management based on the patient's ...
Sulav Pyakurel, Sujan Bohara, Sanjeet Bhattarai, Sachit Regmi, Samikshya Karki, Mahima Adhikari, Bibek Gurung, Umid Shrestha   +7 more
doaj   +3 more sources

Severe Hepatic and Pulmonary Involvement in Rendu-Osler-Weber Syndrome [PDF]

Case Reports in Gastroenterology, 2018
We report the case of a young woman with hereditary hemorrhagic telangiectasia (HHT) with severe liver involvement and pulmonary shunting. The medical imaging in this patient illustrates the severe shunting that can occur in these patients who often are ...
Xavier Verhelst, Anja Geerts, Hans Van Vlierberghe, Peter Smeets, Clarisse Lecluyse   +4 more
doaj   +6 more sources

Rendú Osler Weber Syndrome; case report [PDF]

Radiology Case Reports, 2022
Hereditary hemorrhagic telangiectasia (HHT), or Rendu-Osler-Weber disease, is a dominant autosomal disease characterized by the presence of multiple telangiectasia in skin and mucus, associated with arteriovenous malformations (AVM) of various organs ...
Oscar Manuel García Córdova, MD, Tania Cristina Pérez Morales, MD, Verónica Andrea del Pilar Barón Hernández, MD, José Sebastián Sotelo Cuéllar, MD   +3 more
doaj   +2 more sources

Severe osteomalacia with multiple insufficiency fractures secondary to intravenous iron therapy in a patient with Rendu-Osler-Weber syndrome [PDF]

Bone Reports, 2020
Summary: This case report describes a 65-year-old man with a Rendu-Osler-Weber syndrome with secondary chronic anaemia, who received multiple intravenous (IV) iron infusions and sustained diffuse bone pain secondary to multiple insufficiency fractures ...
Eduardo Luis Callejas-Moraga, Enrique Casado, Marta Gomez-Nuñez, Ana Paula Caresia-Aroztegui   +3 more
doaj   +2 more sources

Pulmonary arteriovenous malformations in Rendu-Osler-Weber syndrome. [PDF]

J Vasc Bras
Abstract Rendu-Osler-Weber syndrome, also known as hereditary hemorrhagic telangiectasia, is an autosomal dominant hereditary disorder. It is characterized by presence of multiple arteriovenous malformations (AVMs) and telangiectasias. This article reports two cases of patients with Rendu-Osler-Weber syndrome who had pulmonary AVMs and underwent ...
de Araújo-Gomes CF, Virgini-Magalhães CE, de Castro LS, Rodrigues EO, Bezerra AA, Mayall MR, Riguetti-Pinto CR, Fagundes FB.   +7 more
europepmc   +3 more sources

Pancytopenia in a Patient with Rendu-Osler-Weber Syndrome and Uncommon Vascular Abnormalities. [PDF]

Case Rep Hematol, 2016
Rendu-Osler-Weber syndrome, or hereditary hemorrhagic teleangiectasia (HHT), is a rare autosomal dominant vascular disorder, characterized by multiple mucocutaneous teleangiectases with recurrent nasal and gastrointestinal bleedings and/or solid-organ arteriovenous shunts.
Binello N, Gasbarrini A, Gaetani E.
europepmc   +5 more sources