Published online Dec 16, 2015. doi: 10.12998/wjcc.v3.i12.973
Peer-review started: May 21, 2015
First decision: August 16, 2015
Revised: September 26, 2015
Accepted: October 12, 2015
Article in press: October 13, 2015
Published online: December 16, 2015
Processing time: 201 Days and 15.5 Hours
Facial nerve palsy is a condition with several implications, particularly when occurring in childhood. It represents a serious clinical problem as it causes significant concerns in doctors because of its etiology, its treatment options and its outcome, as well as in little patients and their parents, because of functional and aesthetic outcomes. There are several described causes of facial nerve paralysis in children, as it can be congenital (due to delivery traumas and genetic or malformative diseases) or acquired (due to infective, inflammatory, neoplastic, traumatic or iatrogenic causes). Nonetheless, in approximately 40%-75% of the cases, the cause of unilateral facial paralysis still remains idiopathic. A careful diagnostic workout and differential diagnosis are particularly recommended in case of pediatric facial nerve palsy, in order to establish the most appropriate treatment, as the therapeutic approach differs in relation to the etiology.
Core tip: Pediatric facial nerve palsy can be congenital or acquired and its etiology can remain unknown. Bell’s palsy is the most frequent form of facial paralysis also in children; about 70% of these cases has a favorable prognosis with spontaneous resolution. An accurate differential diagnosis is necessary to assess the prognosis and the therapeutic options. In Bell’s palsy, the use of oral corticosteroids is recommended also in children, preferably within 3 d from onset. In children presenting a permanent congenital or acquired facial palsy, the therapeutic strategy consists in surgical techniques associated to rehabilitative approaches.