Effect of pulmonary arteriovenous malformations on the mechanical properties of the lungs

Autor: Cécile Rotenberg, Marcel Bonay, Mostafa El Hajjam, Sandra Blivet, Alain Beauchet, Pascal Lacombe, Thierry Chinet

Publikováno v: BMC Pulmonary Medicine, Vol 17, Iss 1, Pp 1-4 (2017)

Abstract Background Pulmonary arteriovenous malformations (PAVMs) are present in approximately 15–50% individuals with hereditary hemorrhagic telangiectasia (HHT). They may be isolated but more often are multiple. The goal of this study was to eval

Externí odkaz: https://doaj.org/article/4078645d5a2946b691029e451aa7f8b6

Superior vena cava syndrome: do not miss the Ariadne’s thread

Autor: Mostafa El Hajjam,, Pierre Yves Marcy,, Alexis Lacout,, Juliette Thariat,, Pascal Lacombe

Publikováno v: Diagnostic and Interventional Radiology, Vol 19, Iss 1, Pp 70-72 (2013)

A central venous catheter tip located too high into the superior vena cava (SVC) is known to be a strong risk factor for central venous thrombosis and subsequent SVC syndrome. We report herein the usefulness of catheterizing the implanted port cathet

Externí odkaz: https://doaj.org/article/6c5e1bbaf08e40f49781a12e469e34f1

Higher prevalence of splenic artery aneurysms in hereditary hemorrhagic telangiectasia: Vascular implications and risk factors

Autor: Mostafa El Hajjam, Florent Soubrier, Augustin Ozanne, Gilles Lesur, Alain Beauchet, Philippe Charron, Pascal Lacombe, Aurélien Palmyre, Isabelle Bourgault-Villada, Jerome Lucas, Jérome Lesniak, Axel Dallongeville, Carole Fagnou, J. Sellier, Carma Karam, S. Binsse, Thierry Chinet, Mélanie Eyries, Sandra Blivet, Agnès Nicod-Tran

Publikováno v: PLoS ONE
PLoS ONE, Public Library of Science, 2020, 15 (1), pp.e0226681. ⟨10.1371/journal.pone.0226681⟩
PLoS ONE, Vol 15, Iss 1, p e0226681 (2020)

International audience; Background: Splenic artery aneurysm (SAA) is a rare but potentially fatal condition. Rupture results in 25% mortality up to 75% in pregnant women with 95% fetal mortality. Brief reports suggest an increased risk of developing

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5adef5cc0995e9e23cbbe4f6e33efdb
https://hal.sorbonne-universite.fr/hal-02945460/file/journal.pone.0226681.pdf

Executive summary of the 11th HHT international scientific conference

Autor: Urban W. Geisthoff, Helen M. Arthur, Pascal Lacombe, Whitney Wooderchak-Donahue, Beth L. Roman, Scott O. Trerotola, Sebastiaan Velthuis, Christopher C.W. Hughes, Mary E. Meek, James R. Gossage, Paul Oh

Publikováno v: Angiogenesis. 18:511-524

Hereditary hemorrhagic telangiectasia (HHT) is a hereditary condition that results in vascular malfor- mations throughout the body, which have a proclivity to rupture and bleed. HHT has a worldwide incidence of about 1:5000 and approximately 80 % of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64da1037f6d438c43b7b4a1817debe29
https://doi.org/10.1007/s10456-015-9482-5

Prenatal molecular diagnosis in RASA1-related disease

Autor: Philippe Charron, Stéphanie Staraci, Mélanie Eyries, Pascal Lacombe, Philippe Dufour, Florent Soubrier, Marie-Victoire Senat, Augustin Ozanne, Thierry Chinet, Aurélien Palmyre

Publikováno v: Prenatal diagnosis. 37(12)

RASA1-related disease is a rare autosomal dominant disease characterized by capillary malformations, arteriovenous malformations (AVMs), and/or arteriovenous fistulas (AFVs). Penetrance is nearly complete and vascular malformations may cause serious

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b892b25e711989ee856e2ceadeb89f2
https://pubmed.ncbi.nlm.nih.gov/29025196