ArticleSudanese journal of paediatrics2018
Pulmonary arteriovenous malformation in a neonate: a condition commonly misdiagnosed.
Article in Sudanese journal of paediatrics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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4 citing papers in PubMed, 4 citations in OpenAlex.
- Evaluation of a gradually enlarging complex pulmonary arteriovenous malformation consisting of innumerable small fistulae using four-dimensional computed tomography.BMJ case reports · 2024Article
- Sudden pediatric death unveiling pulmonary arteriovenous malformations.Autopsy & case reports · 2024Article
- Pulmonary arteriovenous malformation with unexplained cyanosis as the first presentation of hereditary haemorrhagic telangiectasia, case report, and literature review.European heart journal. Case reports · 2021Article
- Giant Neonatal Pulmonary Arteriovenous Malformation: An Imaging and Management Challenge.CASE (Philadelphia, Pa.) · 2020Article
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Authors and funding
4 authors at 2 institutions in 2 countries.
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Abstract
Pulmonary arteriovenous malformations (PAVMs) are congenital defects in the form of an anomalous bridging between a pulmonary arterial and venous system that sidesteps the normal pulmonary capillary. This anomaly is usually associated with hereditary hemorrhagic telangiectasia, leftover small group are sporadic cases but may occur as an isolated anomaly or as multiple lesions. Rarely, such abnormalities can be acquired. Few cases are diagnosed in the neonatal period, as it will pass silent without symptoms. Clinical manifestations occur soon after birth as cyanosis, tachypnea, and an abnormal sound as bruit over the AVM; and the most important point is the clinical suspicion of diagnosis in absence of pulmonary parenchymal and cardiac disease that can explain the persistence of cyanosis. We report a successful Amplatzer vascular plug occlusion of isolated multiple left side PAVM in a neonate, which was done on two stages with a 6 months interval, with no complications. Over 2-year follow-up, the patient remained well with no symptoms.
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