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A rare case report of frontoethmoidal encephalocele in a neonate
by
Kibru, Ermias Algawork
, Mogessie, Yidnekachew Girma
in
Birth defects
/ Case Report
/ Case reports
/ Encephalocele
/ Females
/ Frontoethmoidal
/ Medicine
/ Medicine & Public Health
/ Neonatal neurology
/ Neural tube defects
/ Neurosurgery
/ Skin
/ Surgical neonate
/ Tomography
2023
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A rare case report of frontoethmoidal encephalocele in a neonate
by
Kibru, Ermias Algawork
, Mogessie, Yidnekachew Girma
in
Birth defects
/ Case Report
/ Case reports
/ Encephalocele
/ Females
/ Frontoethmoidal
/ Medicine
/ Medicine & Public Health
/ Neonatal neurology
/ Neural tube defects
/ Neurosurgery
/ Skin
/ Surgical neonate
/ Tomography
2023
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
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A rare case report of frontoethmoidal encephalocele in a neonate
by
Kibru, Ermias Algawork
, Mogessie, Yidnekachew Girma
in
Birth defects
/ Case Report
/ Case reports
/ Encephalocele
/ Females
/ Frontoethmoidal
/ Medicine
/ Medicine & Public Health
/ Neonatal neurology
/ Neural tube defects
/ Neurosurgery
/ Skin
/ Surgical neonate
/ Tomography
2023
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A rare case report of frontoethmoidal encephalocele in a neonate
Journal Article
A rare case report of frontoethmoidal encephalocele in a neonate
2023
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Overview
Background
The protrusion of cranial contents via a skull defect is known as an encephalocele. Unlike western countries where occipital encephalocele dominates, anterior encephaloceles are the most common types of encephalocele in Southeast Asia, parts of Russia, and Central Africa. We present the clinical presentation and surgical management of an 8-day-old infant with frontoethmoidal encephalocele.
Case presentation
An 8-day-old neonate born to a 24-year-old mother with no antenatal follow-up was referred with a compliant of frontonasal swelling which was present since birth. Physical examination of the neonate revealed a cystic lobulated swelling over the upper edge of the nasal bridge. Computed tomography imaging showed an anterior skull defect, resulting in frontonasal meningoencephalocele. The patient underwent a one-stage operation, which combined nasal-coronal approach with frontal craniotomy, to remove the dysplastic tissue and reconstruct the defect. The patient had successful recovery period with acceptable cosmesis.
Conclusion
We presented a case of frontoethmoidal encephalocele, which is rare in western countries but whose incidence is relatively higher in African countries. Perinatal care is necessary for prevention and early detection of such cases. Direct surgical repair is still the main mode of intervention.
Publisher
Springer Berlin Heidelberg,Springer Nature B.V,SpringerOpen
Subject
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