Results 1 to 10 of about 3,300 (212)

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,
Vasileios Rafailidis,,, EDiR, Anastasios Kartas, Konstantinos Kouskouras   +2 more
exaly   +4 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

Rendu-Osler-Weber disease: a gastroenterologist’s perspective [PDF]

Orphanet Journal of Rare Diseases, 2019
Hereditary hemorrhagic teleangectasia (HHT, or Rendu-Osler-Weber disease) is a rare inherited syndrome, characterized by arterio-venous malformations (AVMs or Telangiectasia). The most important and common manifestation is nose bleeds (epistaxis).
Annalisa Tortora, Maria Elena Riccioni, Eleonora Gaetani, Veronica Ojetti, Grainne Holleran, Antonio Gasbarrini   +5 more
doaj   +5 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 Hepatic and Pulmonary Involvement in Rendu-Osler-Weber Syndrome. [PDF]

Case Rep Gastroenterol, 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 ...
Verhelst X, Geerts A, Van Vlierberghe H, Smeets P, Lecluyse C.   +4 more
europepmc   +4 more sources

Pulmonary arteriovenous malformation revealing Osler‐Weber‐Rendu disease: A case report

Clinical Case Reports (discontinued), 2022
Osler‐Weber‐Rendu disease is a genetic disease characterized by mucocutaneous and visceral telangiectasias. Pulmonary arteriovenous malformation is one of the main visceral complications revealing Osler‐Weber‐Rendu disease. The present case was a 34‐year‐
Herveat
exaly   +2 more sources

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

Bone Rep, 2020
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. Laboratory
Callejas-Moraga EL, Casado E, Gomez-Nuñez M, Caresia-Aroztegui AP.   +3 more
europepmc   +3 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

The Rendu-Osler-Weber Disease Revealed by a Refractory Hypoxemia and Severe Cerebral Fat Embolism [PDF]

Case Reports in Critical Care, 2013
The Rendu-Osler-Weber disease is a genetic disease which may lead to severe hemorrhage and less frequently to severe organ dysfunction. We report the case of a 22-year-old patient with no personal medical history who was involved in a motorcycle accident
Leonel Barreto, Jean-Bernard Amiel, Anthony Dugard, Nicolas Pichon, Marc Clavel, Bruno François, Philippe Vignon   +6 more
doaj   +2 more sources

Enfermedad de Rendu-Osler-Weber Rendu-Osler-Weber syndrome

Revista Cubana de Medicina, 2009
La telangiectasia hemorrágica hereditaria o enfermedad de Rendu-Osler-Weber es autosómica dominante, se caracteriza por la presencia de múltiples telangiectasias en piel y mucosas asociadas a malformaciones arteriovenosas de distintos órganos.
Gloria Astencio Rodríguez, Onix César Garib Alpízar, José Napoleón Ventura Blanco, Boris L. Torres Cueva, Nancy de León Rubio, Jorge Luis Hernández   +5 more
doaj   +1 more source