Document Type
Article
Publication Date
12-16-2024
Publication Title
Journal of Neurosurgery: Case Lessons
Abstract
BACKGROUND Camurati-Engelmann disease (CED) is an extremely rare autosomal dominant genetic disorder that can cause increased intracranial pressure (ICP) secondary to cranial hyperostosis, which decreases intracranial volume. Surgical procedures to reduce ICP in medically refractory cases include intracranial volume expansion and ventriculoperitoneal shunting. OBSERVATIONS The authors present the case of a pediatric patient with CED and medically refractory increased ICP who underwent unilateral hemicraniectomy with titanium cranioplasty, resulting in a complete long-term resolution of symptoms. LESSONS Unilateral hemicraniectomy with titanium cranioplasty is a feasible surgical treatment for CED in pediatric patients with medically refractory increased ICP and papilledema.
PubMed ID
39680872
Volume
8
Issue
25
Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-No Derivative Works 4.0 International License.
Recommended Citation
Guillen-Arguello, Roboan; Sader, Nicholas; and McComb, J. Gordon, "Unilateral hemicraniectomy with titanium cranioplasty for the treatment of high intracranial pressure in a pediatric patient with Camurati-Engelmann disease: illustrative case" (2024). School of Medicine Faculty Publications. 3303.
https://digitalscholar.lsuhsc.edu/som_facpubs/3303
10.3171/CASE24590
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Nervous System Diseases Commons, Neurology Commons, Neurosurgery Commons, Pediatrics Commons