Li X Y, Liu Y, Zhao D H, Liu Y, Sun J J
Department of Otolaryngology Head and Neck Surgery, Sixth Medical Center of The PLA General Hospital, Beijing, China.
J Laryngol Otol. 2022 May;136(5):391-395. doi: 10.1017/S0022215121002334. Epub 2021 Sep 8.
The aim of the present study was to perform a retrospective review of the lesion sites in congenital middle-ear cholesteatoma and any accompanying ossicular defects, as well as to explore the possible aetiology of congenital middle-ear cholesteatoma associated with such ossicular chain defects.
The clinical characteristics and pathogenic mechanisms of ossicular chain defects were investigated in 10 patients with early-stage congenital middle-ear cholesteatoma confirmed by surgery, from August 2011 to February 2019.
Monofocal cholesteatoma was located in the anterosuperior quadrant in 3 cases and in the posterosuperior quadrant in 7 cases; all 10 cases showed an absence of the long crus of incus, and 8 cases showed a complete or partial absence of stapes superstructure. The lesions were confined to the vestibular window and the stapes region and had no contact with the long crus of the incus or stapes in nine cases. None of the 10 patients had any recurrence of cholesteatoma.
Although cholesteatoma can cause erosion of ossicles, the present cases suggest that residual epithelium of the cholesteatoma may coexist with ossicular malformations. Therefore, the aetiology of the clinical characteristics in these patients may derive from residual epithelial hinderance of ossicle development.
本研究旨在对先天性中耳胆脂瘤的病变部位及任何伴随的听骨缺损进行回顾性分析,并探讨与这种听骨链缺损相关的先天性中耳胆脂瘤的可能病因。
对2011年8月至2019年2月期间经手术确诊的10例早期先天性中耳胆脂瘤患者的听骨链缺损的临床特征和发病机制进行了研究。
单灶性胆脂瘤位于前上象限3例,后上象限7例;10例均显示砧骨长脚缺如,8例显示镫骨上结构完全或部分缺如。9例病变局限于前庭窗和镫骨区域,与砧骨长脚或镫骨无接触。10例患者均无胆脂瘤复发。
虽然胆脂瘤可导致听骨侵蚀,但目前的病例表明,胆脂瘤的残留上皮可能与听骨畸形并存。因此,这些患者临床特征的病因可能源于残留上皮对听骨发育的阻碍。