Retroperitoneal Arteriovenous Malformation: A Rare Cause of Pulmonary Hypertension in a Premature Infant

Maksim Zagura, Heleri Konik, Helgi Padari, Tuuli Metsvaht, Toomas Hermlin, Liis Salumae, Tiiu Tomberg

Abstract


Retroperitoneal arteriovenous malformations (AVMs) are rare lesions consisting of dysplastic vessels, which may produce diverse clinical features. We report a case of premature neonate born on the 29th week of gestation, who presented with heart failure, generalized edema, respiratory dyspnea and metabolic acidosis. Digital subtraction angiography revealed a large AVM located adjacent to the aorta and the inferior vena cava. Lumbar arteries supplying the AVM were occluded by coils. The AVM was partially embolized using N-butyl cyanoacrylate. Despite apparently successful embolization procedure, heart failure and respiratory distress progressed. The newborn died on her fourth day of life. We report the first case describing AVM embolization in a very low birth weight preterm infant.




Int J Clin Pediatr. 2015;4(2-3):162-165
doi: http://dx.doi.org/10.14740/ijcp214w


Keywords


Arteriovenous malformation; Preterm infant; Pulmonary hypertension; Hydrops; Embolization; Ultrasound

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International Journal of Clinical Pediatrics, quarterly, ISSN 1927-1255 (print), 1927-1263 (online), published by Elmer Press Inc.                     
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