Cerini R, Faccioli N, Cicconi D, Schenal G, Cugini C, Giarbini N, Colletti V, Pozzi Mucelli R
Istituto di Radiologia, Università di Verona, Policlinico G.B. Rossi, Verona, Italy.
Radiol Med. 2006 Oct;111(7):978-88. doi: 10.1007/s11547-006-0096-2. Epub 2006 Oct 11.
The purpose of this study was to evaluate the reliability of computed tomography (CT) and magnetic resonance imaging (MRI) in characterising cochlear nerve anomalies in auditory brainstem implant candidates with congenital hearing loss.
Seventeen patients affected by congenital sensorineural hearing loss were examined by CT and MRI. Inner ear malformations eligible for auditory brainstem implants were classified according to the Casselman classification. All patients subsequently received auditory brainstem implants.
Suspected congenital anomalies were confirmed by CT and MRI in all 17 patients. There were 5/17 bilateral cochlear nerve aplasias and 12/17 cochleovestibular anomalies. Of these, 5/12 patients had a common cochleovestibular cavity, 2/12 had bilateral cochlear aplasia and cochlear nerve agenesis, 1/12 had type I incomplete partition, 2/12 had type II incomplete partition and 2/12 had cochlear hypoplasia.
Preoperative CT and MRI assessment of patients with sensorineural hearing loss is reliable. MRI provided additional information, identifying the possible absence of cochlear nerve and excluding other central nervous system (CNS) diseases.
本研究旨在评估计算机断层扫描(CT)和磁共振成像(MRI)在先天性听力损失的听觉脑干植入候选者中对耳蜗神经异常进行特征描述的可靠性。
对17例先天性感音神经性听力损失患者进行了CT和MRI检查。符合听觉脑干植入条件的内耳畸形根据卡斯尔曼分类法进行分类。所有患者随后均接受了听觉脑干植入。
17例患者的先天性异常均经CT和MRI证实。其中有5/17例双侧耳蜗神经发育不全,12/17例耳蜗前庭异常。其中,5/12例患者有共同的耳蜗前庭腔,2/12例有双侧耳蜗发育不全和耳蜗神经缺如,1/12例为I型不完全分隔,2/12例为II型不完全分隔,2/12例为耳蜗发育不全。
术前对感音神经性听力损失患者进行CT和MRI评估是可靠的。MRI提供了额外信息,可确定耳蜗神经可能缺失并排除其他中枢神经系统(CNS)疾病。