Miura Makoto, Sando Isamu, Hirsch Barry E, Orita Yorihisa
Elizabeth McCullough Knowles Otopathology Laboratory, Division of Otopathology, Department of Otolaryngology, University of Pittsburgh School of Medicine, Suite 153, Eye and Ear Institute Building, 203 Lothrop Street, 15213, Pittsburgh, PA, USA.
Int J Pediatr Otorhinolaryngol. 2002 Jul 9;64(3):207-16. doi: 10.1016/s0165-5876(02)00070-8.
Two temporal bone-eustachian tube (ET) specimens; one from a 1-day-old female newborn with Townes Syndrome (Case 1) and the other from a 15-year-old female with oral-facial-digital syndrome (Case 2) were studied histopathologically and morphometrically. Both specimens had anomalies of the ET and its associated structures as compared with eight age-matched control cases without anomaly (six cases for Case 1 and two cases for Case 2, respectively). Case 1 had a weak attachment of the tensor veli palatini muscle (TVPM) to a poorly developed lateral lamina (LL) of the ET cartilage, a large voluminous medial lamina (ML) of the ET cartilage, a small voluminous ET lumen with a few ridges of mucosal folds, poorly developed ET glands and a poorly developed levator veli palatini muscle (LVPM). Case 2 had a short and longitudinally elongated ET lumen that was insufficiently covered with a poorly developed ML and LL and an aberrant course of the LVPM. Both cases were accompanied by a mild inner ear anomaly (slightly shortened cochlea). We discuss the implications of the observed anomalies with regard to functional and clinical issues. In particular, we speculate that these ET anomalies may closely be related to potential ET dysfunction with high susceptibility to otitis media.
研究了两个颞骨-咽鼓管(ET)标本;一个来自患有汤姆斯综合征的1日龄女新生儿(病例1),另一个来自患有口面指综合征的15岁女性(病例2),进行了组织病理学和形态学测量。与八个无异常的年龄匹配对照病例(病例1为六个病例,病例2为两个病例)相比,两个标本的咽鼓管及其相关结构均存在异常。病例1中,腭帆张肌(TVPM)与发育不良的咽鼓管软骨外侧板(LL)附着薄弱,咽鼓管软骨内侧板(ML)体积大,咽鼓管管腔小且有少量黏膜皱襞嵴,咽鼓管腺体发育不良,腭帆提肌(LVPM)发育不良。病例2中,咽鼓管管腔短且纵向拉长,发育不良的内侧板和外侧板覆盖不足,腭帆提肌走行异常。两个病例均伴有轻度内耳异常(耳蜗略短)。我们讨论了观察到的异常在功能和临床问题方面的影响。特别是,我们推测这些咽鼓管异常可能与咽鼓管潜在功能障碍密切相关,对中耳炎易感性高。