Results 51 to 60 of about 1,710,432 (174)
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
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 +3 more
doaj +1 more source
Left extended hepatectomy with biliary resection and reconstruction for hilar cholangiocarcinoma in patient with Osler-Rendu-Weber disease: a case report and review of literature. [PDF]
Updates Surg: Osler-Rendu-Weber syndrome is a genetic disease that involves organs, liver included, characterized by alterations in the vessel walls, making them more vulnerable to spontaneous rupture and bleeding indeed.
Marchese A +7 more
europepmc +2 more sources
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
Rendu-Osler-Weber Syndrome: A Case Report [PDF]
, 2014 Hereditary hemorrhagic telangectasia (HHT) or Rendu-Osler-Weber syndrome, is a rare genetic disorder with autosomal dominance and variable penetrance. The typical findings of the disease are telangiectasias in skin and mucous membranes, and arteriovenous
Ignjatović, Vesna +3 more
core +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
Osler-Weber-Rendu sendromu ile ilişkili pulmoner arteriyovenöz malformasyon
, 2011 Osler-Weber-Rendu syndrome is a relatively common vascular displasia of children presented with telengiectasias of skin, mucosa, and visceral organs and arteriovenous malformations.
Aygün Dindar +5 more
core +1 more source