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Published on: October 20, 2017
Craniofacial Encephalocele: Updates on Management
Amelia Alberts1, Brandon Lucke-Wold1
1Department of Neurosurgery, University of Florida, Gainesville, FL 32608, USA.
Insights
Craniofacial encephaloceles, rare neural tissue herniations, cause severe developmental issues. Minimally invasive surgeries show promise for treatment and seizure control.
Area of Science:
- Neuroscience
- Developmental Biology
- Surgical Innovation
Background:
- Craniofacial encephaloceles are rare but severe neurodevelopmental abnormalities.
- Etiology involves genetic factors like Sonic Hedgehog and Wnt signaling pathways.
- Treatment consensus is lacking due to varied surgical techniques.
Purpose of the Study:
- To review current understanding of craniofacial encephalocele etiology.
- To explore evolving surgical approaches for encephalocele repair.
- To discuss minimally invasive techniques for associated temporal seizures.
Main Methods:
- Literature review of genetic factors and surgical interventions.
- Analysis of minimally invasive techniques like HULA and endoscopic endonasal surgery.
- Examination of treatments for drug-resistant temporal seizures, including laser therapy.
Main Results:
- Minimally invasive approaches demonstrate successful outcomes.
- Two-stage operations and endoscopic techniques offer less invasive repair.
- Laser interstitial thermal therapy shows promise for drug-resistant seizures.
Conclusions:
- Advancements in surgical techniques are improving craniofacial encephalocele treatment.
- Minimally invasive options provide effective alternatives to traditional craniotomies.
- Addressing associated seizures with novel therapies is crucial for patient outcomes.
Abstract:
Craniofacial encephaloceles are rare, yet highly debilitating neuroanatomical abnormalities that result from herniation of neural tissue through a bony defect and can lead to death, cognitive delay, seizures, and issues integrating socially. The etiology of encephaloceles is still being investigated, with evidence pointing towards the Sonic Hedgehog pathway, Wnt signaling, glioma-associated oncogene (GLI) transcription factors, and G protein-coupled receptors within primary cilia as some of the major genetic regulators that can contribute to improper mesenchymal migration and neural tube closure. Consensus on the proper approach to treating craniofacial encephaloceles is confounded by the abundance of surgical techniques and parameters to consider when determining the optimal timing and course of intervention. Minimally invasive approaches to encephalocele and temporal seizure treatment have increasingly shown evidence of successful intervention. Recent evidence suggests that a single, two-stage operation utilizing neurosurgeons to remove the encephalocele and plastic surgeons to reconstruct the surrounding tissue can be successful in many patients. The HULA procedure (H = hard-tissue sealant, U = undermine and excise encephalocele, L = lower supraorbital bar, A = augment nasal dorsum) and endoscopic endonasal surgery using vascularized nasoseptal flaps have surfaced as less invasive and equally successful approaches to surgical correction, compared to traditional craniotomies. Temporal encephaloceles can be a causative factor in drug-resistant temporal seizures and there has been success in curing patients of these seizures by temporal lobectomy and amygdalohippocampectomy, but magnetic resonance-guided laser interstitial thermal therapy has been introduced as a minimally invasive method that has shown success as well. Some of the major concerns postoperatively include infection, cerebrospinal fluid (CSF) leakage, infringement of craniofacial development, elevated intracranial pressure, wound dehiscence, and developmental delay. Depending on the severity of encephalocele prior to surgery, the surgical approach taken, any postoperative complications, and the age of the patient, rehabilitation approaches may vary.
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