A Case of Pulmonary Arteriovenous Malformation Presented with Paradoxical Brain Embolism
Author:
Affiliation:
1. Department of Thoracic Surgery, Kita-Harima Medical Center
2. Department of Diagnostic Pathology, Kita-Harima Medical Center
3. Department of Radiology, Kita-Harima Medical Center
Publisher
Japan Surgical Association
Subject
General Engineering
Link
https://www.jstage.jst.go.jp/article/jjsa/80/2/80_282/_pdf
Reference11 articles.
1. 1) Nakayama M, Nawa T, Chonan T, et al : Prevalence of Pulmonary Arteriovenous Malformations as Estimated by Low-Dose Thoracic CT Screening. Intern Med 2012 ; 51 : 1677-1681
2. 2) Shovlin CL, Guttmacher AE, Buscarini E, et al : Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome). Am J Med Genet 2000 ; 91 : 66-67
3. 3) Komiyama M, Terada A, Ishiguro T, et al : Neuroradiological Manifestations of Hereditary Hemorrhagic Telangiectasia in 139 Japanese Patients. Neurol Med Chir (Tokyo) 2015 ; 55 : 479-486
4. 6) Gershon AS, Faughnan ME, Chon KS, et al : Transcatheter embolotherapy of maternal pulmonary arteriovenous malformations during pregnancy. Chest 2001 ; 119 : 470-477
5. 7) Muri JW : Arteriovenous aneurysm of the lung. Am J Surg 1995 ; 89 : 265-271
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