| Literature DB >> 22783011 |
Maria Inês Mascarenhas1, Marta Moniz, Sofia Ferreira, Augusto Goulão, Rosalina Barroso.
Abstract
High-output cardiac failure is rare in newborns. Emergent diagnosis and management of this pathology is crucial. We report the case of a child, currently 12-months old; obstetric background is non-contributory. Clinic observation on D1 was normal except for the presence of a systolic cardiac murmur; cardiological evaluation revealed mild ventricular dysfunction of the right ventricle. On the third day of life, she developed cardiac failure with gallop rhythm, hepatomegaly and a murmur in the anterior fontanel; an echocardiogram confirmed clinic aggravation with biventricular dysfunction and right cavities and superior vena cava dilatation. The cranial MRI confirmed the presence of a pial arteriovenous malformation (AVM) involving the anterior and middle cerebral arteries with an associated fronto-parietal ischaemic lesion. The infant underwent embolisations of AVM with successful flow reduction and cardiac failure improvement. The multidisciplinary follow-up showed no cardiac dysfunction or permanent lesions but confirmed a severe psycho-motor delay and left hemiparesia.Entities:
Mesh:
Year: 2012 PMID: 22783011 PMCID: PMC4543165 DOI: 10.1136/bcr-2012-006289
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X