Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Congenital pulmonary arteriovenous aneurysm"'
Publikováno v:
Revue Neurologique. 167:29-34
Resume Introduction Les malformations arterioveineuses pulmonaire (MAVP), survenant le plus souvent lors d’une maladie de Rendu Osler (HHT), se compliquent dans 5 a 13 % des cas d’un abces cerebral. Observation Un homme âge de 51 ans, cadre supe
Publikováno v:
Journal de Radiologie. 88:367-376
Resume Objectifs Rapporter notre experience de l’embolisation dans le traitement des formes localisees de fistules arterioveineuses pulmonaires chez l’adulte. Materiel et methods Tous les patients presentant une forme localisee de fistules arteri
Publikováno v:
Revue des Maladies Respiratoires. 21:131-135
Resume Introduction Les fistules arterio-veineuses pulmonaires (FAVP) sont des malformations vasculaires rares, le plus souvent d’origine congenitale. Parmi les causes de FAVP acquises, l’origine traumatique est exceptionnelle. Cas clinique Nous
Autor:
Timothy S. Hall, Kirk D. Jones, Jeffery Katz, Peter Anastassiou, Michael J. Mann, Miranda J Kramer, David M. Jablons, Jeffrey A. Golden
Publikováno v:
The Journal of Thoracic and Cardiovascular Surgery. 127(2):574-576
J Thorac Cardiovasc Surg Katz, Jeffrey Golden, Kirk Jones and David M. Jablons Michael J. Mann, Miranda J. Kramer, Timothy S. Hall, Peter Anastassiou, Jeffery Isolated pulmonary arteriovenous malformations requiring anatomic resection http://jtcs.cts
Publikováno v:
Journal of the Belgian Society of Radiology; Vol 94, No 2 (2011); 90
Journal of the Belgian Society of Radiology, Vol 94, Iss 2 (2011)
Journal of the Belgian Society of Radiology, Vol 94, Iss 2 (2011)
A 37-year old patient with Rendu-Osler-Weber syndrome presented to our hospital with hypoxy.
Publikováno v:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques. 38(1)
Autor:
Reed E. Pyeritz, Scott O. Trerotola
Publikováno v:
AJR. American journal of roentgenology. 195(4)
OBJECTIVE. Pulmonary arteriovenous malformations (PAVMs) are most often associated with hereditary hemorrhagic telangiectasia. Untreated, they represent a serious threat due to paradoxical embolization that may manifest as stroke or brain abscess. PA
Autor:
W. H. Beierwaltes, F. X. Byron
Publikováno v:
Journal of the American Medical Association. 134(13)
In 1938 the attention of the members of the medical profession was first called by Rodes1to congenital pulmonary arteriovenous aneurysm with secondary polycythemia as a cause of cyanosis. Since this first report only 7 of these cases have been report
Publikováno v:
European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery. 36(2)
Autor:
Hikaru Matsuda, Toru Matsushita, Hajime Ichikawa, Yuji Miyamoto, Masamichi Ono, Tomoko Kita, Norihide Fukushima
Publikováno v:
The Annals of thoracic surgery. 77(5)
We report an 8-year-old girl whose unilateral pulmonary arteriovenous fistula (PAVF) disappeared after we redirected hepatic venous blood to the affected lung. This case provides strong evidence that formation of a PAVF depends only on the presence o