Sequential Management of Pierre Robin Sequence: Case Report
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons
;
: 270-275, 2011.
Artigo
em Coreano
| WPRIM
| ID: wpr-785067
ABSTRACT
Pierre Robin Sequence (PRS) is known as an anomaly consisting of respiratory obstruction with glossoptosis, micrognathia and cleft palate in a newborn. The etiology of PRS is not known, but several factors may be involved simultaneously. Mortality rate of PRS is about 5~30% and the treatment method is divided into both conventional treatments and surgical interventions. If the respiratory obstruction is not resolved by the conventional method, surgical treatment, such as subperiosteal release of the floor of the mouth, tongue-lip adhesion, tracheostomy, distraction osteogenesis may be needed. This study reports a case of PRS in a newborn male at 20 days, with dyspnea and feeding difficulties. Clinical examination showed micrognathia with glossoptosis and cleft palate as the typical PRS triad. We tried surgical intervention with subperiosteal release of the floor of the mouth and tongue-lip adhesion and surgery was successful. At 19th months, we also repaired the incomplete cleft palate successfully using 2-Flap palatoplasty.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Síndrome de Pierre Robin
/
Traqueostomia
/
Fissura Palatina
/
Osteogênese por Distração
/
Aves Canoras
/
Dispneia
/
Pisos e Cobertura de Pisos
/
Boca
Limite:
Humanos
/
Masculino
/
Recém-Nascido
Idioma:
Coreano
Revista:
Journal of the Korean Association of Maxillofacial Plastic and Reconstructive Surgeons
Ano de publicação:
2011
Tipo de documento:
Artigo
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