Results 41 to 50 of about 654,931 (251)

Hereditary haemorrhagic telangiectasia and pulmonary arteriovenous malformations

open access: yesBMJ Case Reports, 2021
Hereditary haemorrhagic telangiectasia (HHT) also known as Osler-Weber-Rendu syndrome is an autosomal dominant disorder affecting 1 in 8000 individuals.
L. Dunphy, A. Talwar, N. Patel, A. Evans
semanticscholar   +1 more source

Hemangioma – A pointer to Abernethy syndrome?

open access: yesAnnals of Pediatric Cardiology, 2020
Diffuse pulmonary arteriovenous malformations or pulmonary arterial hypertension (PAH) may result from congenital portosystemic venous shunts. Hemangioma as a physical sign of congenital portosystemic shunts (like Abernethy syndrome) has not been ...
Shyam S Kothari
doaj   +1 more source

Pulmonary Arteriovenous Malformations [PDF]

open access: yesAmerican Journal of Respiratory and Critical Care Medicine, 2014
Abstract Within the past decade, pulmonary arteriovenous malformations (PAVMs) have evolved from rare curiosities to not uncommon clinical states, with the latest estimates suggesting a prevalence of ∼1 in 2,600. PAVMs provide anatomic right-to-left shunts, allowing systemic venous blood to bypass gas exchange and pulmonary capillary ...
openaire   +3 more sources

Emergency hepatectomy for hepatic arteriovenous malformation combined with pulmonary hypertension in an infant

open access: yesJournal of Pediatric Surgery Case Reports, 2015
Patients with hepatic arteriovenous malformations rarely present with pulmonary hypertension. We report the case of a 3-month-old boy who developed severe pulmonary hypertension due to a hepatic arteriovenous malformation.
Naruhiko Murase   +8 more
doaj   +1 more source

Sudden pediatric death unveiling pulmonary arteriovenous malformations. [PDF]

open access: yesAutops Case Rep
Pulmonary arteriovenous malformations (PAVMs) are abnormal vascular connections between pulmonary arteries and veins, often associated with hereditary hemorrhagic telangiectasia (HHT).
Abu-El-Rub H   +4 more
europepmc   +2 more sources

Management of Pulmonary Arteriovenous Malformations [PDF]

open access: yesSeminars in Interventional Radiology, 2011
Pulmonary arteriovenous malformations are rare lesions with significant clinical complications. These lesions are commonly seen in patients with hereditary hemorrhagic telangiectasia (formerly Osler-Weber-Rendu syndrome). Interventional radiologists are a key part of the treatment team in this complex disease, and a thorough understanding of the ...
Mary E, Meek   +2 more
openaire   +2 more sources

Baseline characteristics of patients with pulmonary arteriovenous malformations.

open access: yes, 2022
Baseline characteristics of patients with pulmonary arteriovenous malformations.
Young-Ok Na (14204628)   +13 more
core   +1 more source

Giant pulmonary arteriovenous malformation [PDF]

open access: yesEuropean Journal of Cardio-Thoracic Surgery, 2004
A 44-year-old man was admitted with coughing and dyspnea for 3 weeks. Chest radiography and thoracic CT scanning confirmed a huge left lung arteriovenous malformation (Fig. 1). Due to a prohibitively high operative risk, he was investigated with pulmonary angiography in preparation for embolization therapy (Fig. 2). The patient subsequently refused all
Sihoe, ADL   +3 more
openaire   +4 more sources

Approach to Pulmonary Arteriovenous Malformations: A Comprehensive Update

open access: yesJournal of Clinical Medicine, 2020
Pulmonary arteriovenous malformations (PAVMs) are abnormal direct vascular communications between pulmonary arteries and veins which create high-flow right-to-left shunts.
S. Majumdar, J. McWilliams
semanticscholar   +1 more source

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

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   +1 more source

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