Literature DB >> 24148537

Occasional finding of a dural arteriovenous fistula in a newborn with orbital lymphangioma. A case report.

E Ventura1, F Ormitti, A Summa, R Menozzi, D Cerasti, G Crisi.   

Abstract

Dural arteriovenous fistulas (DAVF) are vascular malformations rarely occurring in the paediatric population (1,2,3). Prompt diagnosis and treatment are mandatory to prevent life-threatening complications including congestive heart failure and severe brain injury (1,2). We describe the case of a female newborn with an orbital lymphangioma treated for a posterior fossa DAVF. We emphasize the role of MR imaging as a useful non-invasive tool in the diagnosis of these malformations and in the evaluation of associated brain parenchymal lesions.

Entities:  

Year:  2010        PMID: 24148537     DOI: 10.1177/197140091002300207

Source DB:  PubMed          Journal:  Neuroradiol J        ISSN: 1971-4009


  1 in total

1.  Giant cavernous malformation of the posterior fossa with lymphangiomatous phenotype, associated with orbital venolymphatic anomaly in an 11-month-old patient: case report and literature review.

Authors:  Jose Daniel Flores-Sanchez; Ivethe Pregúntegui; Carlos Ugas; Carla Cruzado; Alberto Ramirez; Julio A Poterico
Journal:  Childs Nerv Syst       Date:  2022-07-29       Impact factor: 1.532

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.