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Neonatal Developmental Venous Anomalies: Clinicoradiologic Characterization and Follow-Up.
Geraldo, A F; Messina, S S; Tortora, D; Parodi, A; Malova, M; Morana, G; Gandolfo, C; D'Amico, A; Herkert, E; Govaert, P; Ramenghi, L A; Rossi, A; Severino, M.
Afiliação
  • Geraldo AF; From the Neuroradiology Unit (A.F.G.), Centro Hospitalar de Vila Nova de Gaia/Espinho, Vila Nova de Gaia, Portugal.
  • Messina SS; Neuroradiology Unit (A.F.G., D.T., G.M., A.R., M.S.).
  • Tortora D; Radiology Unit (S.S.M.), Casa di Cura Regina Pacis, Palermo, Italy.
  • Parodi A; Neuroradiology Unit (A.F.G., D.T., G.M., A.R., M.S.).
  • Malova M; Neonatal Intensive Care Unit (A.P., M.M., L.A.R.).
  • Morana G; Neonatal Intensive Care Unit (A.P., M.M., L.A.R.).
  • Gandolfo C; Neuroradiology Unit (A.F.G., D.T., G.M., A.R., M.S.).
  • D'Amico A; Interventional Unit (C.G.), IRCCS Istituto Giannina Gaslini, Genova, Italy.
  • Herkert E; Dipartimento di Scienze Biomediche Avanzate (A.D.), Universita' Federico II, Napoli, Italy.
  • Govaert P; Division of Neonatology (E.H., P.G.), Department of Paediatrics, Erasmus University Medical Centre, Rotterdam, the Netherlands.
  • Ramenghi LA; Division of Neonatology (E.H., P.G.), Department of Paediatrics, Erasmus University Medical Centre, Rotterdam, the Netherlands.
  • Rossi A; Neonatal Intensive Care Unit (A.P., M.M., L.A.R.).
  • Severino M; Neuroradiology Unit (A.F.G., D.T., G.M., A.R., M.S.) andrearossi@gaslini.org.
AJNR Am J Neuroradiol ; 41(12): 2370-2376, 2020 12.
Article em En | MEDLINE | ID: mdl-33093132
ABSTRACT
BACKGROUND AND

PURPOSE:

Although developmental venous anomalies have been frequently studied in adults and occasionally in children, data regarding these entities are scarce in neonates. We aimed to characterize clinical and neuroimaging features of neonatal developmental venous anomalies and to evaluate any association between MR imaging abnormalities in their drainage territory and corresponding angioarchitectural features. MATERIALS AND

METHODS:

We reviewed parenchymal abnormalities and angioarchitectural features of 41 neonates with developmental venous anomalies (20 males; mean corrected age, 39.9 weeks) selected through a radiology report text search from 2135 neonates who underwent brain MR imaging between 2008 and 2019. Fetal and longitudinal MR images were also reviewed. Neurologic outcomes were collected. Statistics were performed using χ2, Fisher exact, Mann-Whitney U, or t tests corrected for multiple comparisons.

RESULTS:

Developmental venous anomalies were detected in 1.9% of neonatal scans. These were complicated by parenchymal/ventricular abnormalities in 15/41 cases (36.6%), improving at last follow-up in 8/10 (80%), with normal neurologic outcome in 9/14 (64.2%). Multiple collectors (P = .008) and larger collector caliber (P < .001) were significantly more frequent in complicated developmental venous anomalies. At a patient level, multiplicity (P = .002) was significantly associated with the presence of ≥1 complicated developmental venous anomaly. Retrospective fetal detection was possible in 3/11 subjects (27.2%).

CONCLUSIONS:

One-third of neonatal developmental venous anomalies may be complicated by parenchymal abnormalities, especially with multiple and larger collectors. Neuroimaging and neurologic outcomes were favorable in most cases, suggesting a benign, self-limited nature of these vascular anomalies. A congenital origin could be confirmed in one-quarter of cases with available fetal MR imaging.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Malformações Vasculares Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Newborn Idioma: En Revista: AJNR Am J Neuroradiol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Portugal

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Malformações Vasculares Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Newborn Idioma: En Revista: AJNR Am J Neuroradiol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Portugal