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Repair of Frontoethmoidal Encephalocele in the Philippines: An Account of 30 Cases Between 2008-2013.

Identifieur interne : 000106 ( Main/Exploration ); précédent : 000105; suivant : 000107

Repair of Frontoethmoidal Encephalocele in the Philippines: An Account of 30 Cases Between 2008-2013.

Auteurs : Amanda-Lynn Marshall [États-Unis] ; Pradeep Setty [États-Unis] ; Mark Hnatiuk [États-Unis] ; Daniel R. Pieper [États-Unis]

Source :

RBID : pubmed:28344182

Descripteurs français

English descriptors

Abstract

BACKGROUND

Frontoethmoidal encephalocele is a congenital abnormality of the anterior skull base involving herniation of cranial contents through a midline skull defect. Patency of the foramen cecum, along with other multifactorial variables, contributes to the development of frontoethmoidal encephaloceles. Because of limited resources, financial constraints, and lack of surgical expertise, repair of frontoethmoidal encephaloceles is limited in developing countries.

METHODS

Between 2008 and 2013 an interdisciplinary team composed of neurosurgeons, craniofacial surgeons, otolaryngologists, plastic surgeons, and nursing personnel, conducted surgical mission trips to Davao City in Mindanao, Philippines. All patients underwent a combined extracranial/intracranial surgical approach, performed in tandem by a neurosurgeon and a craniofacial surgeon, to detach and remove the encephalocele. This procedure was followed by reconstruction of the craniofacial defects.

RESULTS

A total of 30 cases of frontoethmoidal encephalocele were repaired between 2008 and 2013 (20 male; 10 female). The average age at operation was 8.7 years, with 7 patients older than 17 years. Of the 3 subtypes, the following breakdown was observed in patients: 18 nasoethmoidal; 9 nasofrontal; and 3 naso-orbital. Several patients showed concurrent including enlarged ventricles, arachnoid cysts (both unilateral and bilateral), and gliotic changes, as well as orbit and bulbus oculi (globe) deformities. There were no operative-associated mortalities or neurologic deficits, infections, or hydrocephalus on follow-up during subsequent trips.

CONCLUSIONS

Despite the limitations of performing advanced surgery in a developing country, the combined interdisciplinary surgical approach has offered effective treatment to improve physical appearance and psychological well-being in afflicted patients.


DOI: 10.1016/j.wneu.2017.03.063
PubMed: 28344182


Affiliations:


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Le document en format XML

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<term>Arnold-Chiari Malformation (epidemiology)</term>
<term>Child (MeSH)</term>
<term>Child, Preschool (MeSH)</term>
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<term>Encephalocele (epidemiology)</term>
<term>Encephalocele (surgery)</term>
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<term>Nasal Bone (surgery)</term>
<term>Neurosurgeons (MeSH)</term>
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<term>Otolaryngologists (MeSH)</term>
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<term>Femelle (MeSH)</term>
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<term>Nourrisson (MeSH)</term>
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<term>Os ethmoïde (imagerie diagnostique)</term>
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<p>
<b>BACKGROUND</b>
</p>
<p>Frontoethmoidal encephalocele is a congenital abnormality of the anterior skull base involving herniation of cranial contents through a midline skull defect. Patency of the foramen cecum, along with other multifactorial variables, contributes to the development of frontoethmoidal encephaloceles. Because of limited resources, financial constraints, and lack of surgical expertise, repair of frontoethmoidal encephaloceles is limited in developing countries.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>Between 2008 and 2013 an interdisciplinary team composed of neurosurgeons, craniofacial surgeons, otolaryngologists, plastic surgeons, and nursing personnel, conducted surgical mission trips to Davao City in Mindanao, Philippines. All patients underwent a combined extracranial/intracranial surgical approach, performed in tandem by a neurosurgeon and a craniofacial surgeon, to detach and remove the encephalocele. This procedure was followed by reconstruction of the craniofacial defects.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>A total of 30 cases of frontoethmoidal encephalocele were repaired between 2008 and 2013 (20 male; 10 female). The average age at operation was 8.7 years, with 7 patients older than 17 years. Of the 3 subtypes, the following breakdown was observed in patients: 18 nasoethmoidal; 9 nasofrontal; and 3 naso-orbital. Several patients showed concurrent including enlarged ventricles, arachnoid cysts (both unilateral and bilateral), and gliotic changes, as well as orbit and bulbus oculi (globe) deformities. There were no operative-associated mortalities or neurologic deficits, infections, or hydrocephalus on follow-up during subsequent trips.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
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<p>Despite the limitations of performing advanced surgery in a developing country, the combined interdisciplinary surgical approach has offered effective treatment to improve physical appearance and psychological well-being in afflicted patients.</p>
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<Keyword MajorTopicYN="N">Foramen cecum</Keyword>
<Keyword MajorTopicYN="N">Frontoethmoidal encephalocele</Keyword>
<Keyword MajorTopicYN="N">Neural tube defect</Keyword>
<Keyword MajorTopicYN="N">Pediatric craniofacial reconstruction</Keyword>
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<Year>2017</Year>
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<Year>2017</Year>
<Month>03</Month>
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<PubMedPubDate PubStatus="accepted">
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<name sortKey="Marshall, Amanda Lynn" sort="Marshall, Amanda Lynn" uniqKey="Marshall A" first="Amanda-Lynn" last="Marshall">Amanda-Lynn Marshall</name>
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<name sortKey="Hnatiuk, Mark" sort="Hnatiuk, Mark" uniqKey="Hnatiuk M" first="Mark" last="Hnatiuk">Mark Hnatiuk</name>
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