Prenatal Diagnosis of Fetal Nasal Glioma
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Abstract
A34-year-old primigravida with no significant medical
history underwent a routine ultrasound at 21 weeks’
gestation. Fetal sonography revealed the presence of a solid
mass, 14 mm 19 mm in size, arising from the region of
the glabella (Figure 1B). No other abnormalities were
detected. Fetal MRI was performed at 21 weeks
(Figure 2A) to clearly define the lesion and rule out
calvarial defects. The patient chose to continue with the
pregnancy. A male fetus was uneventfully delivered at 39
weeks. The presence of a solid friable mass located in the
left internal canthus was noticed (Figure 2B). The mass
was resected with no complications at 2 weeks of age
(Figure 2C), and pathological study confirmed the presence
of neuroglial heterotopic tissue (nasal glioma). Although
benign in nature, gliomas are cosmetically unfavorable, and
early surgical intervention is the treatment of choice to
minimize nasal distortion.1,2 Differential diagnosis includes
encephalocele, teratoma, dermoid cyst, dacryocystocele,
retinoblastoma, and hemangioma.2,3 Prenatal suspected
diagnosis and assessment is of paramount relevance
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Bibliographic citation
Mendez-Gallart et al. Prenatal Diagnosis of Fetal Nasal Glioma. Journal of Obstetrics and Gynaecology Canada ,40, 5: 523 - 524
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https://doi.org/10.1016/j.jogc.2017.02.002Sponsors
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© 2017 The Society of Obstetricians and Gynaecologists of Canada/La Société des obstétriciens et gynécologues du Canada. Published by Elsevier Inc. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/







