Ajmera Ankit, John Nikeith, Morey Adrienne, Biggs Nigel, Flanagan Sean, Earls Peter, Brown Daniel, Mukherjee Payal
ENT Department, Sydney Adventist Hospital, Sydney, NSW, Australia.
Department of Anatomical Pathology, ACT Pathology, Canberra Hospital, Canberra, ACT, Australia.
Eur Arch Otorhinolaryngol. 2024 Dec 26. doi: 10.1007/s00405-024-09160-4.
Meniere's disease (MD) is a disabling disease of the inner ear, having a substantial effect on a patient's quality of life. While various postulations regarding its aetiology exists, due to the difficulty with accessing inner ear tissue, there have been limited histological studies in patients with active MD.
Tissue was collected during labyrinthectomy from 8 patients with intractable MD who had failed medical therapy (22 samples), and 9 patients undergoing translabyrinthine resection of vestibular schwannoma (19 samples). 20 additional samples were obtained from 2 cadavers without a history of inner ear disease. Samples were assessed with routine histology and a panel of immunohistochemical markers to assess any differences between the groups.
No MD samples demonstrated significant inflammatory infiltrate, evidence of denervation of the sensory epithelium, fibrosis, or thickening of blood vessel wall stroma. Novel findings included confirmation that no lymphatic channels of usual type were present and that the subepithelial stromal cells are strongly positive for S100, suggesting possible perineurial origin. There were no consistent differences in expression of Claudin or Aquaporin between the MD and VS patient samples.
This is one of the largest comparative histological study utilising operative samples from inner ear of living donors with active intractable MD and control patients with VS. There were no significant morphological differences between the two groups, suggesting that the aetiology lies elsewhere within the vestibular system. Examination of endolymphatic sac tissue is therefore a priority for future work.
梅尼埃病(MD)是一种使人衰弱的内耳疾病,对患者的生活质量有重大影响。尽管关于其病因有多种假设,但由于获取内耳组织存在困难,活动性梅尼埃病患者的组织学研究有限。
从8例药物治疗无效的顽固性梅尼埃病患者(22个样本)的迷路切除术中收集组织,以及从9例接受经迷路前庭神经鞘瘤切除术的患者(19个样本)中收集组织。另外从2例无内耳疾病史的尸体中获取20个样本。对样本进行常规组织学和一组免疫组化标记物评估,以评估各组之间的差异。
梅尼埃病样本均未显示出明显的炎性浸润、感觉上皮去神经支配的证据、纤维化或血管壁基质增厚。新发现包括确认不存在通常类型的淋巴管,且上皮下基质细胞S100呈强阳性,提示可能起源于神经束膜。梅尼埃病患者样本和前庭神经鞘瘤患者样本之间Claudin或水通道蛋白的表达没有一致差异。
这是利用来自活动性顽固性梅尼埃病活体供体和前庭神经鞘瘤对照患者内耳手术样本进行的最大规模比较组织学研究之一。两组之间没有明显的形态学差异,这表明病因存在于前庭系统的其他部位。因此,内淋巴囊组织检查是未来工作的重点。