Results 41 to 50 of about 411,420 (197)
Síndrome de Osler Weber Rendau en adulto mayor
, 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
core +1 more source
A Spinal Arteriovenous Fistula in a 3-Year Old Boy
Case Reports in Pediatrics, 2014 We present a case of a 3-year-old boy with neurodegeneration. Family history reveals Rendu-Osler-Weber disease. Magnetic resonance imaging (MRI) of the spinal cord and spinal angiography showed a spinal ...
Thomas E. M. Crijnen +6 more
doaj +1 more source
Case of Osler-Weber-Rendu Syndrome Complicated with Nasal Septum Perforation
Central Asian Journal of Medical Sciences, 2020 Objectives: Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease) is a rare autosomal dominant disorder characterized by multiple mucocutaneous telangiectasias and visceral arteriovenous malformations.
Odgerel Tsogbadrakh +4 more
doaj +1 more source
Enfermedad de Rendu Osler Weber: presentación de un caso
Galicia Clínica, 2021 La Telangiectasia Hemorrágica Hereditaria o Enfermedad de Rendu-Osler- Weber, es una entidad infradiagnosticada y el retraso diagnóstico es fre- cuente, lo que va a difi el screening y tratamiento preventivo de los pacientes y de sus familiares afectos ...
Ana Arévalo Gómez +3 more
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
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
Ischemic cholangitis during Osler-Weber-Rendu disease: a case report
Egyptian Liver Journal, 2022 Background Osler-Weber-Rendu disease (OWRD) is a rare autosomal dominant genetic disease that causes skin and mucosal telangiectasias and visceral arteriovenous malformations.
Oussama Kharmach +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
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
Anaesthesia Reports, Volume 14, Issue 1, January‐June 2026.Summary A pregnant woman with hereditary haemorrhagic telangiectasia was referred to the obstetric anaesthetic team to determine the safety of neuraxial labour analgesia. International guidelines state that the risk of complications from spinal vascular malformations during neuraxial procedures is theoretical and recommend against routine imaging of ...
V. Pinkert +3 more
wiley +1 more source