Results 41 to 50 of about 1,710,432 (184)
Síndrome de Osler Weber Rendau en adulto mayor [PDF]
, 2022 Objective: To expose the main clinical characteristics to make the diagnosis of Hereditary hemorrhagic telangiectasia or Osler-Weber-Rendu syndrome. Case presentation: We present the case of a 70-year-old patient with a history of repeated epistaxis who ...
Esteban Badillo, Laura Yibeth +4 more
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Massive Hemothorax by Ruptured Arteriovenous Malformation [PDF]
Modern MedicineIntroduction and objectives: Osler Weber Rendu disease is a rare genetic disorder characterized by multiple telangiectasias and arteriovenous malformations involving parenchymatous organs, leading to hemorrhagic, sometimes life threatening vascular ...
Genoveva CADAR, Otilia RADU
doaj +1 more source
Pulmonary arteriovenous malformationsm and follow-up imagings
The Pan African Medical Journal, 2020 An 85-year-old caucasian female with past medical history of hypertension, hyperlipidemia, polymyalgia rheumatica, coronary artery disease, Osler-Weber-Rendu syndrome (diagnosed 18 years ago), intermittent epistaxis and pulmonary arteriovenous ...
Pahnwat Tonya Taweesedt, Salim Surani
doaj +1 more source
Osler-Weber-Rendu Syndrome [PDF]
, 2019 Yetmiş dört yaşındaki erkek olgu, yüzünde ve oral mukozada telenjiyektaziler ve sık burun kanaması şikâyetiyle polikliniğimize başvurdu. Olgunun öz geçmişinde, iki kere mide kanaması geçirdiği ve sık burun kanama öyküsü olduğu anlaşıldı.
An, İsa, İsa AN
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The role of nuclear medicine in a case of Rendu–Osler–Weber disease with pulmonary involvement
World Journal of Nuclear Medicine, 2021 Rendu–Osler–Weber syndrome or hereditary hemorrhagic telangiectasia (HHT) is a rare systemic disease. Its primary pathogenic expression is multiple arteriovenous malformations (AVM) and severe hypoxia.
Carlyle Barral +3 more
doaj +1 more source
Thalidomide as an effective treatment in a case of Osler Weber Rendu syndrome: a case report
Asian Journal of Medical Sciences, 2016 Osler Weber Rendu Syndrome (OWRS), or Hereditary Hemorrhagic telangiectasia (HHT) is an autosomal dominant disease presents with epistaxis, telangiactesia and multiorgan vascular dysplasia.
Titli Bandyopadhyay
doaj +1 more source
Endoscopic Classification of Severe Spontaneous Epistaxis: A Case‐Series of 445 Patients
Laryngoscope Investigative Otolaryngology, Volume 11, Issue 2, April 2026.Epistaxis can be related to several histopathological findings. ABSTRACT Objective To identify the anatomical location and characterize the histopathological findings of severe spontaneous epistaxis through endoscopic evaluation and tissue biopsy.
Wen Zhang +2 more
wiley +1 more source
Anais Brasileiros de Dermatologia, 2005 Relato de um caso de úlcera plantar por fístula arteriovenosa em paciente portador de telangiectasia hemorrágica hereditária ou doença de Rendu-Osler-Weber tratado com ácido tranexâmico.
Gabriella Corrêa de Albuquerque +4 more
doaj +1 more source
Novel Simplified Nasal Endoscopy Grading System for Hereditary Hemorrhagic Telangiectasia Patients
The Laryngoscope, Volume 136, Issue 2, Page 652-657, February 2026.We validated a novel, simplified nasal endoscopy grading system for patients with Hereditary Hemorrhagic Telangiectasia (HHT). Our grading (mild, moderate, severe) demonstrated strong correlation with Epistaxis Severity Score (ESS) and Quality of Life (QoL), and showed substantial inter‐rater reliability (ICC = 0.8).
Ethan Soudry +4 more
wiley +1 more source
Síndrome de Osler-Weber-Rendu [PDF]
, 2013 Homem, 68anos, com história de anemia e episódios frequentes de epistaxe e obstrução nasal pouco responsivos à terapêutica usual, apresentava telangiectasias nas mucosas nasal e oral.
Torres, Felipe Soares +4 more
core +3 more sources