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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

[Rendu-Osler-Weber disease]. [PDF]

Nederlands tijdschrift voor tandheelkunde, 2005
Rendu-Osler-Weber disease or hereditary hemorrhagic telangiectasia (HHT) is a multisystem autosomal dominant hereditary disorder. The disorder is manifested by multiple dysplasia of blood vessels of the skin and mucous membranes. This results in recurrent and sometimes severe bleeding, of which epistaxis is the most common.
Sys, L.M., Hoogen, F.J.A. van den
openaire   +4 more sources

Síndrome de Osler-Weber-Rendu [PDF]

Clinical and Biomedical Research, 2013
Homem, 68anos, com história de anemia e episódios frequentes de epistaxe e obstrução nasal pouco responsivos à terapêutica usual, apresentava telangiectasias nas mucosas nasal e oral.
Maurício Farenzena, Amalia Izaura Nair Medeiros Klaes, Andre Anjos, Jefferson Andre Bauer, Felipe Soares Torres   +4 more
doaj   +6 more sources

Pulmonary arteriovenous malformations in Rendu-Osler-Weber syndrome. [PDF]

J Vasc Bras
Abstract Rendu-Osler-Weber syndrome, also known as hereditary hemorrhagic telangiectasia, is an autosomal dominant hereditary disorder. It is characterized by presence of multiple arteriovenous malformations (AVMs) and telangiectasias. This article reports two cases of patients with Rendu-Osler-Weber syndrome who had pulmonary AVMs and underwent ...
de Araújo-Gomes CF, Virgini-Magalhães CE, de Castro LS, Rodrigues EO, Bezerra AA, Mayall MR, Riguetti-Pinto CR, Fagundes FB.   +7 more
europepmc   +3 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   +2 more sources

Severe Hepatic and Pulmonary Involvement in Rendu-Osler-Weber Syndrome. [PDF]

Case Rep Gastroenterol, 2018
We report the case of a young woman with hereditary hemorrhagic telangiectasia (HHT) with severe liver involvement and pulmonary shunting. The medical imaging in this patient illustrates the severe shunting that can occur in these patients who often are asymptomatic.
Verhelst X, Geerts A, Van Vlierberghe H, Smeets P, Lecluyse C.   +4 more
europepmc   +6 more sources

Recurrent Gastrointestinal Bleeding in a Man with Osler-Weber-Rendu Syndrome and Intestinal Varices [PDF]

Canadian Journal of Gastroenterology, 1988
A patient with Osler-Weber-Rendu disease and idiopathic intestinal varices who presented with recurrent gastrointestinal hemorrhage and iron deficiency anemia is reported. The unique coexistence of these two rare disorders is discussed and the literature
Robert N. Clark, William G. Paterson, Laurington R. DaCosta, Ivan T. Beck   +3 more
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

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   +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   +2 more sources