<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>67(5)</volume><submitter>Rajesh GN</submitter><pubmed_abstract>Pulmonary arteriovenous malformations (AVM) are very rare and carry the risk of cerebral thrombo-embolism, brain abscess or pulmonary hemorrhage. The Amplatzer vascular plug II (AVP II) is a new device, used for embolization of the pulmonary AVMs. We report a case of pulmonary AVM successfully managed by using AVP II in a patient with hereditary hemorrhagic telangiectasia (HHT).</pubmed_abstract><journal>Indian heart journal</journal><pagination>455-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4593798</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Device closure of pulmonary arteriovenous malformation using Amplatzer vascular plug II in hereditary hemorrhagic telangiectasia.</pubmed_title><pmcid>PMC4593798</pmcid><pubmed_authors>Rajesh GN</pubmed_authors><pubmed_authors>Haridasan V</pubmed_authors><pubmed_authors>Krishnan MN</pubmed_authors><pubmed_authors>Sajeer K</pubmed_authors><pubmed_authors>Nair A</pubmed_authors><pubmed_authors>Sajeev CG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Device closure of pulmonary arteriovenous malformation using Amplatzer vascular plug II in hereditary hemorrhagic telangiectasia.</name><description>Pulmonary arteriovenous malformations (AVM) are very rare and carry the risk of cerebral thrombo-embolism, brain abscess or pulmonary hemorrhage. The Amplatzer vascular plug II (AVP II) is a new device, used for embolization of the pulmonary AVMs. We report a case of pulmonary AVM successfully managed by using AVP II in a patient with hereditary hemorrhagic telangiectasia (HHT).</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Sep-Oct</publication><modification>2025-04-04T13:25:09.734Z</modification><creation>2019-03-27T01:59:32Z</creation></dates><accession>S-EPMC4593798</accession><cross_references><pubmed>26432734</pubmed><doi>10.1016/j.ihj.2015.05.024</doi></cross_references></HashMap>