Results 21 to 30 of about 6,864 (154)

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

Liver transplantation in a patient with hereditary haemorrhagic telangiectasia and pulmonary hypertension

Pulmonary Circulation, 2019
Hereditary haemorrhagic telangiectasia or Rendu-Osler-Weber syndrome is a systemic vascular disease with autosomal dominant inheritance, mucocutaneous telangiectasia, and repeated nasal bleeding due to vascular abnormalities.
Kentaro Ejiri, Satoshi Akagi, Kazufumi Nakamura, Naofumi Amioka, Keishi Ichikawa, Takahito Yagi, Hiroshi Ito   +6 more
doaj   +1 more source

Pulmonary arteriovenous malformation revealing Osler‐Weber‐Rendu disease: A case report

Clinical Case Reports, 2022
Osler‐Weber‐Rendu disease is a genetic disease characterized by mucocutaneous and visceral telangiectasias. Pulmonary arteriovenous malformation is one of the main visceral complications revealing Osler‐Weber‐Rendu disease. The present case was a 34‐year‐
Herveat Ramanandafy, Finaritra Princy Parfait Andriamahenina, Michel Harison Tiaray, Anjara Mihaja Nandimbiniaina, Angela Zamelina Razafindrasoa, Sonia Razafimpihanina, Diamondra Andriarimanga, Jean Noêl Solohery Ratsimbazafy, Jocelyn Robert Rakotomizao, Joëlson Lovaniaina Rakotoson, Hanta Marie Danielle Vololontiana   +10 more
doaj   +1 more source

Haemothorax in a Pregnant Woman Secondary to Rupture of a Pulmonary Arteriovenous Malformation

European Journal of Case Reports in Internal Medicine, 2022
Pulmonary arteriovenous malformations (PAVMs) are abnormal communications between the arteries and veins of the pulmonary vasculature leading to a right-to-left shunt.
Melissa van den Bulck, Claude Berenger Ngah, Hyppolyte Ntula, Yilmaz Gorur, Benoît Cardos, Denis Brisbois, Noel Lorenzo Villalba, Deeba Ali   +7 more
doaj   +1 more source

Successful treatment of bilateral multiple pulmonary arteriovenous malformations in a patient with brain abscess and severe hypoxemia using a combination of transcatheter embolotherapy and surgical resection: a case report

Journal of Cardiothoracic Surgery, 2021
Background A pulmonary arteriovenous malformation is an abnormal dilated blood vessel that makes direct communication between a pulmonary artery and pulmonary vein and can be associated with hypoxemia or neurological complications, including brain ...
Takahiro Ochi, Masako Chiyo, Takamasa Ito, Hideharu Furumoto, Toshihiko Sugiura, Yukio Saitoh   +5 more
doaj   +1 more source

Malformações arteriovenosas pulmonares – Associação a telangiectasia hemorrágica hereditária. Casos clínicos e rastreio familiar

Revista Portuguesa de Pneumologia, 2006
Resumo: As malformações arteriovenosas pulmonares são raras e mais de metade dos casos surgem em associação a telangiectasia hemorrágica hereditária.Faz-se uma revisão teórica sobre a apresentação clínica, abordagem diagnóstica, terapêutica
Diva Ferreira, Joana Amado, Raquel Duarte, José Almeida, Paulo Morgado, Teresa Shiang   +5 more
doaj   +1 more source

Arterial desaturation due to pulmonary arteriovenous malformations after the Kawashima Operation

Annals of Pediatric Cardiology, 2016
Arterial desaturation may occur after the Kawashima procedure and, in the absence of venovenous collaterals is usually due to pulmonary arteriovenous malformations.
Rohit S Loomba
doaj   +1 more source

Pulmonary arteriovenous malformation. [PDF]

American Journal of Roentgenology, 1996
A 46-year-old man with facial telangiectasias and recurrent epistaxis had worsening dyspnea on exertion. Laboratory examination revealed chronic hypoxemia and secondary polycythemia. A chest radiograph (Fig. 1A) showed a right apical lung opacity. CT (Fig.
C R, Suchin, G J, Whitman, F S, Chew
openaire   +3 more sources

Pulmonary arteriovenous malformations presenting as difficult-to-control asthma: a case report

Journal of Medical Case Reports, 2013
Introduction Although pulmonary arteriovenous malformations are relatively rare disorders, they are an important part of the differential diagnosis of common pulmonary problems, such as hypoxemia, dyspnea on exertion and pulmonary nodules.
Navratil Marta, Vidjak Vinko, Rubić Filip, Erceg Damir, Turkalj Mirjana   +4 more
doaj   +1 more source

Pulmonary arteriovenous malformation in a pediatric patient with epistaxis and hypoxemia

Radiology Case Reports, 2020
Hereditary hemorrhagic telangiectasia (HHT; also known as Osler-Weber-Rendu syndrome) is an inherited vascular disorder with a spectrum of clinical manifestations depending on lesion distribution.
Ryan W. England, MD, Clifford R. Weiss, MD   +1 more
doaj   +1 more source