Results 21 to 30 of about 654,931 (251)

Pulmonary arteriovenous malformations diagnosed through hemoptysis: A case report

Radiology Case Reports, 2021
There have been few reports of pulmonary arteriovenous malformations complicated by hemoptysis. Herein, we present our experience and provided a review of the literature.
Risako Minamikawa, M.D., Yasuji Ryu, M.D., Junichiro Sanada, M.D., Harumi Takata, M.D., Toshiya Okumura, M.D.   +4 more
doaj   +1 more source

Pulmonary arteriovenous malformation [PDF]

Postgraduate Medical Journal, 2002
Abstract Pulmonary arteriovenous malformations (PAVM) are rare pulmonary vascular anomalies. Although most patients are asymptomatic, PAVMs can cause dyspnoea from right-to-left shunt. Because of paradoxical emboli, various central nervous system complications have been described including stroke and brain abscess.
I, Khurshid, G H, Downie
openaire   +2 more sources

Pulmonary arteriovenous malformations may be the only clinical criterion present in genetically confirmed hereditary haemorrhagic telangiectasia

Thorax, 2022
Pulmonary arteriovenous malformations (PAVMs) result in preventable complications demanding specialty care. Underlying hereditary haemorrhagic telangiectasia (HHT) can be identified by genetic testing, if the diagnosis is considered.
Emily Anderson, Lakshya Sharma, A. Alsafi, C. Shovlin   +3 more
semanticscholar   +1 more source

Reperfusion of Pulmonary Arteriovenous Malformations Treated by Catheter Embolization. [PDF]

J Clin Med
Objective: The aim of this study was to evaluate patients with hereditary hemorrhagic telangiectasia (HHT) for the potential reperfusion of pulmonary arteriovenous malformations (PAVM) treated by catheter embolization using coils or embolization plugs ...
Gulich B, Buecker A, Schneider G.
europepmc   +3 more sources

Neurologic Complications in Hereditary Hemorrhagic Telangiectasia with Pulmonary Arteriovenous Malformations: A Systematic Review

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 2022
: Background: Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant multi-organ condition occurring with a 1 in 3800 prevalence in Alberta.
Joel Agarwal, Jennifer T. N. LaBranche, S. Dhillon, W. Allison, T. Jeerakathil, D. Vethanayagam   +5 more
semanticscholar   +1 more source

Pulmonary arteriovenous malformation and inherent complications with solitary lung nodule biopsy—literature overview and case report

Radiology Case Reports, 2022
Pulmonary arteriovenous malformation, also known as an arteriovenous fistula, is typically a congenital disease caused by structural deficiencies, particularly the lack of capillary wall development, leading to the abnormal dilation of the pulmonary ...
Cung-Van Cong, MD, PhD, Dinh-Van Luong, MD, PhD, Tran-Thi Tuan Anh, MD, Nguyen-Le Nhat Minh, MD, Tran-Thi Ly, PhD, Nguyen Minh Duc, MD   +5 more
doaj   +1 more source

A missed case of hereditary hemorrhagic telangiectasia: A case report

SAGE Open Medical Case Reports, 2022
Hereditary hemorrhagic telangiectasia is a rare autosomal dominant disorder characterized by abnormal blood vessel formation. When an abnormal vascular architecture affects the lungs and central nervous system, serious complications can occur.
Jia Zhang, Gaoyun Pan, Yingying Zou, Xiaoshu Chen, Jingye Pan, Yi Wang, Shichao Quan, He Zou   +7 more
doaj   +1 more source

Pulmonary Arteriovenous Malformation and Embolic Myocardial Infarction in a Patient With Hereditary Hemorrhagic Telangiectasia

JACC: Case Reports, 2020
This report describes a case of embolic myocardial infarction secondary to a pulmonary arteriovenous malformation. Pulmonary arteriovenous malformations are rare and mostly congenital and are inherited as an autosomal dominant disorder known as ...
Gabriel Sánchez-Fernández, MD, Fernando García-López, MD, Isaac Martínez-Bendayán, MD, PhD, María José Bello-Peón, MD, Raquel Marzoa-Rivas, MD, PhD   +4 more
doaj   +1 more source

Identification and validation of a novel pathogenic variant in GDF2 (BMP9) responsible for hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations

American Journal of Medical Genetics. Part A, 2021
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant multisystemic vascular dysplasia, characterized by arteriovenous malformations (AVMs), mucocutaneous telangiectasia and nosebleeds. HHT is caused by a heterozygous null allele in ACVRL1,
Srimmitha Balachandar, T. Graves, A. Shimonty, K. Kerr, J. Kilner, S. Xiao, R. Slade, M. Sroya, M. Alikian, E. Curetean, E. Thomas, V. Mcconnell, S. McKee, F. Boardman-Pretty, A. Devereau, T. Fowler, M. Caulfield, E. Alton, T. Ferguson, J. Redhead, A. McKnight, Geraldine A. Thomas, M. Aldred, C. Shovlin   +23 more
semanticscholar   +1 more source

Pulmonary arteriovenous malformation

Journal of the Belgian Society of Radiology, 2011
A 37-year old patient with Rendu-Osler-Weber syndrome presented to our hospital with hypoxy.
Janssens, E, Leyman, P, De Beule, T, Ardies, L, D’haenens, P   +4 more
openaire   +7 more sources