Saito R, Takata N, Matsumoto N, Koide I, Fujita A, Ogura Y, Murakami M, Yanagida K, Komazawa M
Arch Otolaryngol. 1982 Aug;108(8):484-8. doi: 10.1001/archotol.1982.00790560022006.
Histopathological findings in the temporal bone are described in a newborn infant, diagnosed as having Potter's syndrome. The infant has severely malformed low-set ears bilaterally and a small lower jaw; autopsy findings showed bilateral renal agenesis and pulmonary hypoplasia. The temporal bone indicated the deformities of the inner ear, classified as Mondini-type, complicated by extensive deformities to the external ear and middle ear, including absence of auditory ossicles, atresia of the oval window, abnormal course of the facial nerve, and hypoplastic external auditory canal. The cochlear membranous labyrinth showed nearly normal form in the upper turn, but severe hypoplasia in the basal turn, which was an unusual cochlear anomaly.
一名被诊断患有波特综合征的新生儿颞骨组织病理学发现如下。该婴儿双侧耳朵严重畸形且位置较低,下颌较小;尸检结果显示双侧肾缺如和肺发育不全。颞骨显示内耳畸形,分类为Mondini型,并发外耳道和中耳广泛畸形,包括听小骨缺如、卵圆窗闭锁、面神经走行异常以及外耳道发育不全。耳蜗膜迷路在上半圈形态近乎正常,但在下半圈严重发育不全,这是一种不寻常的耳蜗异常。