ArticleOpen medicine (Warsaw, Poland)2015
Pulmonary arterovenous malformation causing hemothorax in a pregnant woman without Osler-Weber-Rendu syndrome.
Article in Open medicine (Warsaw, Poland), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 12 citations in OpenAlex.
- Ruptured pulmonary arteriovenous malformation causing hemothorax during pregnancy: a case report.Journal of cardiothoracic surgery · 2026Article
- Pulmonary arteriovenous malformations as an unusual initial manifestation of gestational trophoblastic neoplasia: a case report from Saudi Arabia.Journal of surgical case reports · 2026Article
- Massive hemothorax induced by pulmonary arteriovenous malformation rupture: a case report and literature review.Journal of cardiothoracic surgery · 2024Review
- Attention to pulmonary arteriovenous fistula in a case of transient hypoxemia and cerebral infarction during pregnancy: a case report and literature review.BMC pregnancy and childbirth · 2023Review
- Spontaneous Hemothorax by Pulmonary Arteriovenous Malformation during Pregnancy.The Thoracic and cardiovascular surgeon reports · 2023Article
- Emergency surgery for hemothorax due to a ruptured pulmonary arteriovenous malformation.General thoracic and cardiovascular surgery · 2020Article
- Pulmonary Arteriovenous Malformations (PAVMs) and Pregnancy: A Rare Case of Hemothorax and Review of the Literature.Case reports in obstetrics and gynecology · 2019Article
- Lobectomy for Pulmonary Arteriovenous Fistula in a Patient With Rendu-Osler-Weber Disease: A Case Report.In vivo (Athens, Greece)Article
Corrections and comments
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Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Pulmonary arteriovenous malformations (PAVMs), although most commonly congenital, are usually detected later in life. CASE REPORT: We present a case of a 19-year-old woman with no previous history of AVM or telangiectasia, who presented dyspnea and hypoxia by massive left hemothorax in the 34th week of gestation. After emergent cesarean delivery, a chest computed tomography (CT) with i.v. contrast showed a likely 3 cm area of active contrast in left lower lung. Chest tube placement revealed about 2 liters of blood. The patient was subsequently found to have pulmonary AVM. A successful embolisation of AVM followed by lung atipic resection involving AVM and decortication for lung re-expansion were the treatments provided.
conclusionsWomen with known pulmonary AVM should be maximally treated prior to becoming pregnant, and the physician should be alert to complications of pulmonary AVM during pregnancy.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.