Nadol Joseph B, Hedley-Whyte E Tessa, Amr Sami Samir, O Apos Malley Jennifer T, Kamakura Takefumi
Department of Otolaryngology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, Massachusetts, USA,
Department of Pathology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Audiol Neurootol. 2018;23(6):326-334. doi: 10.1159/000495176. Epub 2019 Jan 24.
Charcot-Marie-Tooth (CMT) syndrome is a clinically and genetically heterogeneous group of neuropathies affecting both peripheral motor and sensory nerves. Progressive sensorineural hearing loss, vestibular abnormalities, and dysfunction of other cranial nerves have been described. This is the second case report of otopathology in a patient with CMT syndrome. Molecular genetic testing of DNA obtained at autopsy revealed a missense variant in the MPZ gene (p.Thr65Ala), pathogenic for an autosomal-dominant form of CMT1B. The temporal bones were also prepared for light microscopy by hematoxylin and eosin and Gömöri trichome stains, and immunostaining for anti-myelin protein zero. Pathology was consistent with a myelinopathy of the auditory, vestibular, and facial nerves bilaterally. The pathophysiology of cranial nerve dysfunction in CMT is unknown. Findings in the current case suggested, at least in cranial nerves 7 and 8, that a myelinopathy may be causative.
夏科-马里-图思(CMT)综合征是一组临床和遗传异质性的神经病变,累及周围运动和感觉神经。已有报道称患者存在进行性感觉神经性听力丧失、前庭异常以及其他颅神经功能障碍。这是第二例关于CMT综合征患者耳病理学的病例报告。尸检获取的DNA分子遗传学检测显示MPZ基因存在错义变异(p.Thr65Ala),该变异对于常染色体显性形式的CMT1B具有致病性。颞骨也采用苏木精-伊红染色和Gömöri三色染色法进行光镜检查,并进行抗髓磷脂蛋白零免疫染色。病理学结果与双侧听神经、前庭神经和面神经的髓鞘病变一致。CMT中颅神经功能障碍的病理生理学尚不清楚。当前病例的研究结果表明,至少在第7和第8颅神经中,髓鞘病变可能是病因。