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Osler‐Weber‐Rendu syndrome: A case report on a rare vascular malformation presented with lower gastrointestinal bleeding [PDF]

open access: yesClinical Case Reports, 2023
Osler‐Weber‐Rendu syndrome is an uncommon vascular disorder inherited as an autosomal dominant trait with varying penetrance and expression. A multidisciplinary approach is used for a detailed diagnostic workup and management based on the patient's ...
Sulav Pyakurel   +7 more
doaj   +4 more sources

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

open access: yesRadiology 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   +4 more
doaj   +5 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]

open access: yesJA 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   +4 more
doaj   +4 more sources

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

open access: yesEuropean 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   +5 more
doaj   +4 more sources

A Rare Case of Upper Gastrointestinal Bleeding: Osler-Weber-Rendu Syndrome [PDF]

open access: yesMedicina, 2022
Osler-Weber-Rendu disease, also known as hereditary hemorrhagic telangiectasia (HHT), is a rare, autosomal dominant condition that affects approximately 1 in 5000 patients causing abnormal blood vessel formation.
Anna Jargielo   +3 more
doaj   +4 more sources

Osler-Weber-Rendu Syndrome [PDF]

open access: yesIndian Dermatology Online Journal
Arpita N. Rout   +2 more
doaj   +6 more sources

Osler-Weber-Rendu syndrome. [PDF]

open access: yesBMJ Case Rep, 2013
A 57-year-old woman presented to the emergency department reporting of fresh rectal bleeding since 3 days ago. She had a history of spontaneous recurrent epistaxis since childhood but had never been fully evaluated. Her family history was also notable for a son with recurrent spontaneous epistaxis. Physical examination revealed telangiectasia of the …
Abangah G, Rashidbeygi M.
europepmc   +5 more sources

A case of pulmonary arteriovenous malformation in the setting of Rendu Osler Weber syndrome

open access: yesRadiology Case Reports, 2021
Rendu Osler Weber syndrome is a rare disorder, in which arteriovenous malformations are a hallmark feature. We describe the case of a 77-year-old female patient who presented with dyspnea, recurrent epistaxis, and signs of right ventricular heart failure,
Irini Nikolaou, MD   +4 more
doaj   +3 more sources

Hepatic Encephalopathy in Osler-Weber-Rendu Syndrome

open access: yesAnnals 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   +2 more sources

Osler-Weber-Rendu syndrome. [PDF]

open access: yesCMAJ, 2006
The attached image ([Fig. 1][1]) is intended to complement the pulmonary radiography and CT imaging that accompany the report of a case of hereditary hemorrhagic telangiectasia described by Narinder Pal Singh and colleagues.[1][2] It is this observer's experience that telangiectasia have ...
Morphet JA.
europepmc   +4 more sources

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