Results 11 to 20 of about 1,710,432 (184)

Congestive cirrhosis in Osler-Weber-Rendu syndrome: A rare case report

Radiology Case Reports, 2018
Hereditary hemorrhagic telangiectasia or Osler-Weber-Rendu syndrome is a rare autosomal dominant vascular disorder characterized by epistaxis, mucocutaneous telangiectasias, and arteriovenous malformations affecting various organs and systems.
Patrícia Leitão, PhD, André Carvalho, MD, Conceição Guerra, MD, José Gonçalves, MD, Isabel Ramos, PhD   +4 more
doaj   +4 more sources

Osteomalacia Following Iron Infusion Therapy in a Patient With Rendu‐Osler‐Weber Syndrome: F‐18‐FDG PET/CT Discrimination of a Stress Fracture in the Setting of a Musculoskeletal Tumor Mimic [PDF]

Clinical Case Reports
This case report highlights a rare occurrence of osteomalacia induced by hypophosphatemia secondary to ferric carboxymaltose (FCM) therapy in a patient with hereditary hemorrhagic telangiectasia (HHT, or Rendu‐Osler‐Weber syndrome).
Ioannis S. Vasios, Pipitsa N. Valsamaki, Konstantinos Tilkeridis, Savvas Deftereos, Efthymios Iliopoulos   +4 more
doaj   +3 more sources

Enfermedad de Rendu-Osler-Weber Rendu-Osler-Weber syndrome

Revista Cubana de Medicina, 2009
La telangiectasia hemorrágica hereditaria o enfermedad de Rendu-Osler-Weber es autosómica dominante, se caracteriza por la presencia de múltiples telangiectasias en piel y mucosas asociadas a malformaciones arteriovenosas de distintos órganos.
Gloria Astencio Rodríguez, Onix César Garib Alpízar, José Napoleón Ventura Blanco, Boris L. Torres Cueva, Nancy de León Rubio, Jorge Luis Hernández   +5 more
doaj   +2 more sources

Rendu-Osler-Weber syndrome: A family investigation and review

Journal of Indian Academy of Oral Medicine and Radiology, 2009
Rendu-Osler-Weber syndrome is a rare genetic condition characterized by mucocutaneous and visceral fibrovascular dysplasia leading to multiple macular or papular vascular lesions of skin, mucosal surfaces and occasionally viscera that show tendency ...
V G Mahima, Karthikeya Patil, Madhur Kapoor, Shalini Kalia   +3 more
doaj   +3 more sources

OSLER – WEBER – RENDU SYNDROME: A RARE CASE OF UPPER GASTROINTESTINAL BLEEDING [PDF]

Khyber Medical University Journal, 2022
BACKGROUND: Osler-Weber-Rendu syndrome (Hereditary hemorrhagic telengiectasia) cases present with recurrent epistaxis, gastrointestinal bleeding (hematemesis, melena), and arteriovenous malformations involving almost all organs of body.
Farrukh Sher, Muhammad Ahmed Khan, Sumera Akram   +2 more
doaj   +2 more sources

Anesthetic management of a patient with Osler-Weber-Rendu syndrome with multiple pulmonary arteriovenous malformations and pheochromocytoma for femoral artificial bone replacement: a case report [PDF]

JA Clinical Reports, 2023
Background Osler-Weber-Rendu syndrome is characterized by mucocutaneous telangiectasia and arteriovenous malformations in organs. Anesthesia for patients with Osler-Weber-Rendu syndrome is challenging due to complications and physiological changes.
Toshiharu Hiyoshi, Kazuyoshi Shimizu, Satoshi Kimura, Toshiki Naritani, Hiroshi Morimatsu   +4 more
doaj   +3 more sources

Osler-Weber-Rendu syndrome complicated with pulmonary arteriovenous malformation: A case report and review of literatures

Journal of Medical Sciences, 2015
Osler-Weber-Rendu syndrome is a hereditary disease which is diagnosed by criterions of clinical symptoms and examinations. Here, we report a definite case of Osler-Weber-Rendu syndrome who had epistaxis, skin telangiectasia, and pulmonary arteriovenous ...
Kuan-Yu Wang, Jen-Chih Chen, Jane-Yi Hsu
doaj   +2 more sources

Osler-Weber-Rendu Syndrome with Severe Hepatic Manifestations: A Rare Clinical Case [PDF]

European Journal of Case Reports in Internal Medicine, 2020
Rendu-Osler-Weber syndrome is a rare inherited syndrome with autosomal dominant transmission characterized by systemic arteriovenous malformations (AVMs) with multi-organ involvement.
Maria Inês Silva, Clara Matos, Fabio Correia, Sofia Carola, Maria João Gomes, Teresa Branco   +5 more
doaj   +2 more sources

Rendu-Osler-Weber Syndrome: A Case Report [PDF]

Macedonian Journal of Medical Sciences, 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 malformations presenting in the organs like lung, intestine, brain and liver.
Vladimir Vukomanović, Milovan Matović, Vesna Ignjatović, Branislav Belić   +3 more
core   +5 more sources

Pulmonary arteriovenous fistula in the newborn: a case report of Rendu-Osler-Weber syndrome and a review of the literature

The Turkish Journal of Pediatrics, 2001
In most instances, congenital arteriovenous fistula is only one manifestation of a more widespread abnormality; 60% of patients also have hereditary hemorrhagic telangiectasis (Rendu-Osler-Weber syndrome).
R Olguntürk, D Oğuz, S Tunaoğlu, C Ikizler, A Sezgin, S Kula   +5 more
doaj   +4 more sources