Tadmor R, Ravid M, Millet D, Leventon G
AJNR Am J Neuroradiol. 1984 Nov-Dec;5(6):743-5.
During a 3-year period, nine girls and two boys (age range, 2 days-13 years) with congenital choanal atresia were evaluated by computed tomography (CT). Other associated congenital anomalies, primarily craniofacial anomalies, were present in six of the 11 patients. In six patients the atresia was bilateral and consisted of both bony and membranous components. Of the five patients with unilateral atresia, the lesions were on the right in three and on the left in two. CT demonstrated the atresia, choanal stenosis, septal deviation, and thickening of the vomer and palatine bone. The ease of CT examination and the high accuracy of the results make it the preferred imaging method for evaluating choanal atresia.
在3年期间,对9名女孩和2名男孩(年龄范围为2天至13岁)的先天性后鼻孔闭锁进行了计算机断层扫描(CT)评估。11例患者中有6例存在其他相关的先天性异常,主要是颅面异常。6例患者的闭锁为双侧,包括骨性和膜性成分。在5例单侧闭锁患者中,3例病变在右侧,2例在左侧。CT显示了闭锁、后鼻孔狭窄、鼻中隔偏曲以及犁骨和腭骨增厚。CT检查的便捷性和结果的高准确性使其成为评估后鼻孔闭锁的首选成像方法。