| Literature DB >> 20401478 |
Véronica Grzegorczyk1, Marie Brasseur-Daudruy, Gérard Labadie, Cécile Cellier, Eric Verspyck.
Abstract
Nasal glioma is a rare congenital midline malformation composed of heterotopic masses of neuroglial tissue. We report a case of fetal nasal glioma diagnosed by sonography at 22 weeks' gestation as a vascular hypoechoic mass located on the left nasal bone. Fetal MRI excluded an underlying bone defect. At birth, the lesion appeared as a reddish mass. Post natal imaging confirmed the vascularisation within the lesion with an arterial low-flow velocity and a high-resistance spectrum, consistent with a glioma. The child underwent surgery at 5 months and final diagnosis was made on pathological examination. Therefore, a vascular lesion and a clinical aspect mimicking a haemangioma should not be considered sufficient to reach the final diagnosis.Entities:
Mesh:
Year: 2010 PMID: 20401478 DOI: 10.1007/s00247-010-1642-6
Source DB: PubMed Journal: Pediatr Radiol ISSN: 0301-0449