Results 51 to 60 of about 3,185 (193)

Infective endocarditis with Osler’s nodule in a patient with Osler’s disease: a case report and review of the literature

Journal of Medical Case Reports, 2022
Background Hereditary hemorrhagic telangiectasia, also known as Osler–Weber–Rendu disease, induces arteriovenous malformations in visceral organs. Arteriovenous malformations increase the risk of severe infections and are a common complication associated
Genki Naruse, Takatomo Watanabe, Hiroyuki Okura   +2 more
doaj   +1 more source

Variant distribution and characterization of hereditary hemorrhagic telangiectasia in Chinese patients

Eye &ENT Research, Volume 2, Issue 1, Page 53-61, March 2025.
Abstract Background Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disorder with variable manifestations, including recurrent epistaxis, telangiectasias, arteriovenous malformations, and family history. It is caused by heterozygous null alleles of ENG, ACVRL1, SMAD4, or BMP9, with delayed clinical diagnosis.
Yali Zhao, Xiangdong Wang, Yuhui Ouyang, Lin Xi, Yuan Zhang, Yan Zhao   +5 more
wiley   +1 more source

Síndrome Osler-Weber-Rendu. Manejo endoscópico de un sangrado inusual: reporte de caso

Endoscopia, 2021
El síndrome de Osler-Weber-Rendu (OWR), también llamado telangiectasia hemorrágica hereditaria, es un trastorno vascular hereditario que se transmite de manera autosómica dominante con una incidencia de 1 por cada 8,000-16,500 habitantes.
Marcos Cherem-Kibrit, Pablo Gomes da Silva-de Rosenzweig, Francisco de la Vega-González, Rubén Gutiérrez-Alvarado, Óscar Govea-González, Isaías Garduño-Hernández, Francisco J. Ramírez-Amezcua   +6 more
doaj   +1 more source

Approach to anaemia in gastrointestinal disease: A position paper by the ESPGHAN Gastroenterology Committee

Journal of Pediatric Gastroenterology and Nutrition, Volume 80, Issue 3, Page 510-532, March 2025.
Approach to Anaemia in paediatric Gastrointestinal Disease Abstract Anaemia is a frequent consequence of many gastrointestinal (GI) diseases in children and it can even be the initial presenting symptom of underlying chronic GI disease. The definition of anaemia is age and gender‐dependent and it can be classified based on pathophysiology, red cell ...
Ilse Julia Broekaert, Amit Assa, Osvaldo Borrelli, Marco Deganello Saccomani, Matjaž Homan, Javier Martin‐de‐Carpi, Emmanuel Mas, Erasmo Miele, Zrinjka Misak, Sara Sila, Mike Thomson, Christos Tzivinikos, Jernej Dolinsek   +12 more
wiley   +1 more source

Portal Hypertension—Noninvasive Multiparametric Ultrasound‐Based Criteria and Measurements

Portal Hypertension &Cirrhosis, Volume 4, Issue 1, Page 44-65, March 2025.
The review article discusses B‐mode ultrasound (US), color Doppler imaging, arterial Doppler indices, contrast‐enhanced ultrasound (CEUS), endoscopic ultrasound (EUS) and elastography methods in the diagnosis, grading and staging of portal hypertension.
Kathleen Möller, Riyad Abu El Hija, Xiaolong Qi, Christian Jenssen, Sven Mutze, Burkhard Möller, Benjamin Misselwitz, Christoph F. Dietrich   +7 more
wiley   +1 more source

Síndrome de Rendú-Osler-Weber con compromiso gastrointestinal, hepático y pancreático

Revista Colombiana de Gastroenterología
El síndrome de Rendu-Osler-Weber (SROW) se caracteriza por el desarrollo de estructuras vasculares aberrantes, tales como microvasos dilatados y malformaciones arteriovenosas (MAV) en la piel, el tracto gastrointestinal (GI), los pulmones, el hígado, el
Diego Armando Huanay-Martínez, Siomara Aransuzú Chávez Sánchez, Álvaro Bellido-Caparó   +2 more
doaj   +1 more source

Telangiectasia hemorrágica hereditária: ácido tranexâmico no tratamento de úlcera plantar Hereditary hemorrhagic telangiectasia: tranexamic acid for plantar ulcer

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, Célia Regina S. Corrêa de Carvalho, Cristiane R. de Oliveira, Dayse Pereira Terra, Sérgio Soares Quinete   +4 more
doaj   +1 more source

Pulmonary vascular manifestations of hereditary haemorrhagic telangiectasia

Pulmonary Circulation, Volume 14, Issue 4, October 2024.
Abstract Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant, multisystem disorder that manifests with a spectrum of disease including cardiopulmonary complications. HHT is characterised by aberrant signalling via the transforming growth factor β (TGFβ) pathway, with loss of vascular integrity, angiogenesis and vascular dysplasia. The
Sarah Cullivan, Barry Kevane, Brian McCullagh, Terry M. O'Connor, Robin Condliffe, Sean Gaine   +5 more
wiley   +1 more source

ChatGPT Generated Otorhinolaryngology Multiple‐Choice Questions: Quality, Psychometric Properties, and Suitability for Assessments

OTO Open, Volume 8, Issue 3, July–September 2024.
Abstract Objective To explore Chat Generative Pretrained Transformer's (ChatGPT's) capability to create multiple‐choice questions about otorhinolaryngology (ORL). Study Design Experimental question generation and exam simulation. Setting Tertiary academic center.
Cecilia Lotto, Sean C. Sheppard, Wilma Anschuetz, Daniel Stricker, Giulia Molinari, Sören Huwendiek, Lukas Anschuetz   +6 more
wiley   +1 more source

Coexistence of brain capillary telangiectasia and venous angioma: A case report and literature review

Clinical Case Reports, Volume 12, Issue 5, May 2024.
Key Clinical Message While Cerebral vascular malformations exhibit distinct clinical and radiographical features, rare instances of coexisting lesions occur. This case report sheds light on the rare coexistence of brain capillary telangiectasia and venous angioma in a patient presenting with a seizure attributed to frontal lobe bleeding.
Moaz O. Moursi, Anas Alsadi, Yousra Ali, Jouhar Kolleri, Tanweer Hussein   +4 more
wiley   +1 more source