Results 71 to 80 of about 14,655 (208)

Pulmonary Arteriovenous Malformation can be Associated with Embolic Stroke of Undetermined Source (ESUS)

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2019
Pulmonary arteriovenous malformations (PAVMs) are rare vascular anomalies. Alternative designations are pulmonary arteriovenous fistulae or aneurysms. Although mostly asymptomatic, PAVMs can cause respiratory symptoms due to right-to-left shunt.
Mariana Barros Cruz   +3 more
doaj   +1 more source

Prognostic Factors for Postoperative Complications. An Aggregate Protocol for 10 Observational Studies From the Danish TRIPLE‐A Cohort of 1.2 Million Surgeries

open access: yesActa Anaesthesiologica Scandinavica, Volume 70, Issue 7, August 2026.
ABSTRACT Background Postoperative complications substantially increase morbidity, mortality and healthcare costs. Understanding prognostic factors is essential for risk stratification, targeted prevention strategies, and development of prediction models.
Anders Peder Højer Karlsen   +15 more
wiley   +1 more source

Endoscope-integrated indocyanine green videoangiography for craniocervical dural arteriovenous fistula with ruptured anterior spinal artery aneurysm: a case report and review of the literature

open access: yesJournal of Medical Case Reports
Background Treatment for arteriovenous fistulas located at the craniocervical junction involving the pial feeder aneurysm is challenging. When a direct aneurysm manipulation is not feasible, shunt interception to achieve flow reduction is a considerable ...
Tomohisa Ishida   +3 more
doaj   +1 more source

Atrial septal defect with unexplained cyanosis and surprising turn of events-A case report

open access: yesIHJ Cardiovascular Case Reports, 2020
Unexplained cyanosis without any complex congenital heart disease needs further diagnostic work up. We present an adolescent child presenting with unexplained cyanosis who was found to have diffuse pulmonary arteriovenous malformations (PAVMs) due to ...
Jayita Nandy Das   +3 more
doaj   +1 more source

Wyburn‐Mason Syndrome: A Case Report

open access: yes
The Kaohsiung Journal of Medical Sciences, EarlyView.
Yu‐Wen Wang   +2 more
wiley   +1 more source

Air embolism secondary to suspected lymphatic tissue disruption with severe exercise‐induced pulmonary haemorrhage

open access: yesEquine Veterinary Education, Volume 38, Issue 8, Page e501-e508, August 2026.
Summary Air embolism is rare in horses and typically associated with complications following intravenous catheterisation or other medical procedures. Exercise‐induced pulmonary haemorrhage (EIPH) is common in racehorses but not usually associated with air embolism. This report describes a case of air embolism in a 4‐year‐old Thoroughbred with EIPH. The
J. Wittenberg   +7 more
wiley   +1 more source

Fluorescein Angiographic Findings of Peripheral Retinal Vasculature after Intravitreal Conbercept versus Ranibizumab for Retinopathy of Prematurity

open access: yesJournal of Ophthalmology, 2019
Purpose. To evaluate angiographic findings of peripheral retina vasculature in retinopathy of prematurity (ROP) neonates who received intravitreal conbercept (IVC) or ranibizumab (IVR). Methods.
Enzhong Jin   +7 more
doaj   +1 more source

Diagnosis of Parkes Weber syndrome affecting a newborn baby´s upper left limb in a low resource setting: a case report

open access: yesPAMJ Clinical Medicine, 2020
Vascular malformations (VMs) is a term used to describe vessels developmental abnormalities. These malformations involve arteries, veins, capillaries or lymphatics vessels.
Francklin Djifack Tétinou   +5 more
doaj   +1 more source

Endovascular Treatment of Intracranial Pial–Dural Arteriovenous Fistula: A Case Report

open access: yesThe Surgery Journal, 2020
Intracranial pial arteriovenous fistula (PAVF) is a rare cerebrovascular pathology characterized by abnormal direct high-flow connection between the pial or cortical feeding artery and draining vein.
D. V. Shchehlov   +5 more
doaj   +1 more source

Optimizing Diagnostic Accuracy of Clinical Red Flags in RASopathies

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1608-1618, July 2026.
ABSTRACT RASopathies are a group of genetic disorders caused by pathogenic variants in the RAS‐mitogen‐activated protein kinase (RAS–MAPK) signaling pathway, often presenting with congenital heart defects, craniofacial dysmorphisms, and developmental delays. To assess the diagnostic yield of genetic testing in patients with suspected RASopathies and to
Emanuele Bobbio   +16 more
wiley   +1 more source

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