ABSTRACT
Objective Patients with craniocervical junction malformations (CCJM) tend to suffer more frequently from sleep respiratory disturbances, which are more frequent and severe in patients with basilar invagination. Here we evaluate if patients with CCJM and sleep respiratory disorders (SRD) present smaller airway dimensions than patients without SRD. Method Patients with CCCM with and without sleep respiratory disturbances were evaluated clinically by Bindal's score, modified Mallampati classification, full-night polysomnography and upper airway cone beam tomography. Results Eleven patients had sleep respiratory disorders (SRD), and nine patients performed control group without SRD. CCJM patients with SRD were predominantly female, older, had higher BMI, were more likely to have Mallampati grades 3 and 4 and had statistically significant smaller anteroposterior diameter of the upper airway than patients without SRD. Conclusion Patients with CCJM and sleep respiratory disturbances have higher BMI, higher Mallampati score and smaller anterior posterior diameter of the upper airway. .
Objetivo : Pacientes com malformação da transição craniocervical (MTCC) tendem a apresentar mais frequentemente distúrbios respiratórios do sono (DRS), os quais são mais intensos em pacientes com invaginação basilar. O objetivo desse estudo é avaliar se pacientes com MTCC e DRS apresentam dimensões das vias aéreas reduzidas em comparação a pacientes sem DRS. Método : Pacientes com MTCC com e sem apneia do sono foram avaliados com a escala de Bindal, classificação de Mallampati modificada, polissonografia de noite inteira e tomografia da via aérea superior. Resultados Onze pacientes tinham DRS e nove não apresentaram esses distúrbios (grupo controle). Pacientes com MTCC e DRS foram principalmente mulheres, mais velhos, apresentaram maior IMC e maior gradação na escala de Mallampati, além de menor diâmetro anteroposterior de via aérea superior do que pacientes sem DRS. Conclusão Pacientes com MTCC e DRS têm maior IMC, maior pontuação na escala de Mallampati e menor diâmtero anteroposterior da via aérea superior. .
Subject(s)
Adult , Female , Humans , Male , Middle Aged , Arnold-Chiari Malformation/pathology , Arnold-Chiari Malformation/physiopathology , Pharynx/pathology , Pharynx/physiopathology , Sleep Apnea Syndromes/physiopathology , Anthropometry , Case-Control Studies , Cone-Beam Computed Tomography , Organ Size , Polysomnography , Reference Values , Risk Factors , Sex Factors , Statistics, Nonparametric , Time FactorsABSTRACT
The association between pediatric Chiari malformation and the development of syringomyelia has been well documented. Scoliosis in the patient with syringomyelia is thought to be secondary to anterior horn cell damage, which innervate the muscles of trunk, by an asymmetrically expanded syrinx. In pediatric patients, the neurologic signs and symptoms due to Chiari malformation and syringomyelia show much lower frequency but the incidence of scoliosis is very high. Thus, the MRI study for the diagnosis of the underlying syringomyelia and Chiari malfornation is essential in pediatric scoliosis patients, which may otherwise be misdiagnosed for idiopathic scoliosis. We present a case of Chiari type I malformation associated with syringomyelia and scoliosis.