Results 51 to 60 of about 5,408,332 (199)

Hepatic Telangiectases and Portosystemic Encephalopathy in Osler-Weber-Rendu Disease

Gastroenterology, 1968
Summary A patient suffering from hereditary hemorrhagic telangiectases presented with an epigastric bruit and experienced, for 6 months prior to her death, repeated episodes of portosystemic encephalopathy. Angiography demonstrated tremendous dilation of the hepatic arteries and extensive portacaval shunting of blood through telangiectatic channels in
D, Michaeli, I, Ben-Bassat, H I, Miller, V, Deutsch   +3 more
openaire   +2 more sources

Unmasking a Rare Genetic Puzzle: Hereditary Hemorrhagic Telangiectasia in a Black Kenyan Woman: A Case Report

Case Reports in Gastrointestinal Medicine, Volume 2026, Issue 1, 2026.
Background Hereditary hemorrhagic telangiectasia (HHT) is a rare genetic disorder characterized by mucocutaneous and visceral telangiectasias, often leading to severe complications. This case report presents an uncommon manifestation of HHT in a 57‐year‐old Black Kenyan female with upper gastrointestinal bleeding. Given the rarity of HHT in our region,
Lavender Otom, Priyanka Panwar, Farida Kaittany, Ben Clement Lomatayo, Yoshifumi Nakayama   +4 more
wiley   +1 more source

Rendu-Osler-weber disease. Case report [PDF]

, 2016
Rendu-Osler-Weber disease is the most frequently observed genetic hemorrhagic angiopathy with local wall thinning, distention of microcirculation vessels' lumen, and incomplete local hemostasis.
Kurochkin Sergei Vyacheslavovich, Gafurov Marat, Kurochkin S., Gafurov M., Zidikhanov Damir Ilshatovich, Chuvashaev I., Chuvashaev Iskander, Zidikhanov D.   +7 more
core  

Characterizing the Healthcare Utilization and Costs of Hereditary Hemorrhagic Telangiectasia

American Journal of Hematology, Volume 100, Issue 10, Page 1722-1735, October 2025.
ABSTRACT Hereditary hemorrhagic telangiectasia (HHT) is the second‐most common inherited bleeding disorder worldwide, afflicting one in 4000–5000 people, and is the most morbid inherited bleeding disorder of women. HHT causes recurrent severe epistaxis, chronic gastrointestinal bleeding, heavy menstrual bleeding, and arteriovenous malformations in the ...
Hanny Al‐Samkari, Tracy J. Mayne, Misty Troutt, Hemant Patle, Marianne Clancy, Eric Duhaime   +5 more
wiley   +1 more source

Multiple Cerebral Angiomas and Rendu-Osler-Weber Disease: Case Report

, 1991
A 25-year-old man was hospitalized after suffering a subarachnoid hemorrhage. Arteriograms disclosed two arteriovenous malformations, one of which was asymptomatic. Rendu-Osler-Weber disease was suspected because of the concomitant existence of cutaneous
M. Jan, B. Aesch, B. de Toffol, E. Lioret   +3 more
core   +1 more source

RENDU-OSLER-WEBER DISEASE AT 75 YEARS OLD WOMAN

Архивъ внутренней медицины, 2017
The publication presents a clinical case of hereditary hemorrhagic telangiectasia in a woman of 75 years. In the first part of the article, literature data on the incidence and features of Rundu-Osler-Weber disease are presented, modern diagnostic ...
A. S. Barmenova, T. A. Bayesheva, N. S. Umbetalina, V. A. Suhova   +3 more
doaj   +1 more source

Standardization of Terminology, Definitions, and Outcome Criteria for Bleeding in Hereditary Hemorrhagic Telangiectasia: International Consensus Report

American Journal of Hematology, Volume 100, Issue 10, Page 1813-1827, October 2025.
ABSTRACT Hereditary hemorrhagic telangiectasia (HHT, Osler‐Weber‐Rendu disease) is the second most common inherited bleeding disorder worldwide, affecting approximately 1 in 5000 people. Development of disease‐modifying and efficacious hemostatic agents to treat HHT has finally begun after decades without such medical therapies.
Hanny Al‐Samkari, Raj S. Kasthuri, Hans‐Jurgen Mager, Jenny Y. Zhou, Marcelo M. Serra, Bethany T. Samuelson‐Bannow, Layla N. Van Doren, Jay F. Piccirillo, Marianne S. Clancy, Keith R. McCrae, Sonia M. Thomas, Antoni Riera‐Mestre, Allyson M. Pishko, Sarah Sewaralthahab, James R. Gossage, Vivek N. Iyer, Cedric Hermans, Adrienne Hammill, Ingrid Winship, Meir Mei‐Zahav, Annette von Drygalski, Scott Olitsky, Marie E. Faughnan   +22 more
wiley   +1 more source

Hereditary Hemorrhagic Telangiectasia in Pediatric Age: Focus on Genetics and Diagnosis

Pediatric Reports, 2023
Hereditary Hemorrhagic Telangiectasia (HHT) or Rendu–Osler–Weber Syndrome (ROW) is an autosomal dominant vascular disease, with an estimated prevalence of 1:5000.
Cesare Danesino, Claudia Cantarini, Carla Olivieri   +2 more
doaj   +1 more source

Intensity-Modulated Radiotherapy for a Rendu-Osler-Weber Disease Patient with Recurrent Severe Epistaxis: A Case Report [PDF]

, 2010
We present a case of a Rendu-Osler-Weber disease patient with recurrent life threatening epistaxis demanding multiple blood transfusions despite of repetitive endoscopic laser and electrocoagulations, endovascular embolisation, septodermoplasty, and long-
Daniel M. Aebersold, Geretschläger, Andreas, Dubach, Patrick, Maximilian Niyazi, Aebersold, Daniel M, Caversaccio, Marco-Domenico, Marco-Domenico Caversaccio, Andreas Geretschläger, Niyazi, Maximilian, Patrick Dubach, Claus Belka, Blumstein, Norbert M, Andreas Arnold, Arnold, Andreas, Belka, Claus, Patrick Dubach, Norbert M. Blumstein, Marco-Domenico Caversaccio, Andreas Geretschläger   +18 more
core   +4 more sources

Hematochezia: An abnormal presenting symptom of an extensive vascular malformation in a 6‐year‐old boy

JPGN Reports, Volume 6, Issue 3, Page 300-304, August 2025.
Abstract Gastrointestinal (GI) bleeding can be a common symptom in the pediatric population. Vascular malformations, which cause symptoms based on their location and effect on surrounding structures, are an uncommon cause of GI bleeding. We present the case of a 6‐year‐old male with a 1‐year history of hematochezia, constipation, and microcytic anemia.
Kathleen Ordas, Joy Brusenback, Sahana Ummadi, Shannon Tocchio, Razan Alkhouri, Soha Shah   +5 more
wiley   +1 more source