Results 11 to 20 of about 3,300 (212)

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
exaly   +3 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]

Clin Case Rep
ABSTRACT 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). A 21‐year‐old man presented with left tibial pain without prior trauma, accompanied by severe hypophosphatemia ...
Vasios IS, Valsamaki PN, Tilkeridis K, Deftereos S, Iliopoulos E.   +4 more
europepmc   +2 more sources

Rendu-Osler-weber disease. Case report [PDF]

, 2016
Rendu-Osler-Weber disease is the most frequently observed genetic hemorrhagic angiopathy with local wall thinning, distention of microcirculation vessels' lumen, and incomplete local hemostasis.
Chuvashaev I., Gafurov M., Kurochkin S., Zidikhanov D.   +3 more
core   +4 more sources

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

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   +1 more source

Final observation of an extremely severe case of Osler-Weber-Rendu disease in teaching at the pregraduate and postgraduate stages of education and the use of current English-language Internet applications for doctors and patients

Медицина неотложных состояний, 2023
Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome, Osler-Weber-Rendu disease, etc) is diagnosed clinically according to the so called Curacao criteria, if at least three of four of them are present: recurrent spontaneous epistaxis ...
V.M. Rudichenko, N.V. Snigir, V.О. Кrivets   +2 more
doaj   +1 more source

Cerebrovascular Malformations Associated With Hereditary Hemorrhagic Telangiectasia and HHT-Like Syndromes: A Comparative Overview. [PDF]

Eur J Neurol
Hereditary hemorrhagic telangiectasia (HHT) and several HHT‐like syndromes, including Wyburn–Mason, Cobb, Klippel–Trénaunay, Parkes Weber, neurofibromatosis type 1, PHACE(S), capillary malformation–AVM (CM‐AVM), Juvenile polyposis/HHT overlap, HHT type 5, PTEN hamartoma tumor syndrome, and blue rubber bleb nevus syndrome, share overlapping ...
Palermo M, Sturiale CL.
europepmc   +2 more sources

Hepatic Encephalopathy in Osler-Weber-Rendu Syndrome

Annals of Internal Medicine: Clinical Cases, 2022
Hereditary hemorrhagic telangiectasia or Osler-Weber-Rendu syndrome is a rare condition that leads to multiple vascular malformations. We describe the interesting patient case of a woman with recurrent epistaxis secondary to Osler-Weber-Rendu syndrome ...
Sakthi Gautham, Christopher J. Haas
doaj   +1 more source

Rendu-Osler-Weber Syndrome: case report and literature review [PDF]

Brazilian Journal of Otorhinolaryngology, 2008
Juares AJ, Dell'Aringa AR, Nardi JC, Kobari K, Gradim Moron Rodrigues VL, Perches Filho RM.   +5 more
exaly   +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

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   +1 more source

Epistaxis e Hemorragia Digestiva Recorrente: Manifestação da Síndrome Osler-Weber-Rendu

Gazeta Médica, 2020
A telangiectasia hemorrágica hereditária ou síndrome Osler-Weber-Rendu é uma doença vascular hereditária autossómica dominante, que se apresenta, geralmente, com telangiectasias mucocutâneas, epistaxe, hemorragia gastrointestinal, anemia ferripriva e ...
Marisa Isabel de Sousa Ferreira Rosete, Margarida Gaudêncio, Susana Magalhães, Fernando Ferraz e Sousa, Amélia Pereira   +4 more
doaj   +1 more source