Published online Jan 6, 2020. doi: 10.12998/wjcc.v8.i1.175
Peer-review started: October 17, 2019
First decision: November 11, 2019
Revised: November 18, 2019
Accepted: November 27, 2019
Article in press: November 27, 2019
Published online: January 6, 2020
Processing time: 76 Days and 10.4 Hours
Congenital palate perforation is extremely rare. There is controversy about its exact etiology and appropriate management. Here, a case of congenital palatal perforation is reported. The diagnosis and treatment of the disease are summarized.
A full-term neonate boy was referred for oral and craniomaxillofacial surgery with a finding of a hole in the palate at birth. The operation was postponed after pediatric consultation because of the patient’s poor nutrition and underweight for his age. At the age of 10 mo, the patient underwent modified von Langenbeck palatoplasty. He was followed for four years after surgery without any signs of re-rupture. His speech was satisfactory.
Considering the anatomy and etiology, congenital palate perforation can be classified as isolated or associated with submucous cleft palate, and the treatment procedure should be altered accordingly.
Core tip: Rare cases of congenital palate perforation have been described in the literature. There is not a consensus for its etiology and treatment. Successful treatment of a case of congenital palate perforation is presented in this paper. The diagnosis and critical point of surgery are summarized.