Hatano Miyako, Ito Makoto, Sugimoto Hisashi, Noda Masao, Hasegawa Hiroki, Yoshizaki Tomokazu
Department of Otolaryngology-Head and Neck Surgery, Kanazawa University, Kanazawa, Ishikawa, Japan.
Department of Pediatric Otolaryngology, Jichi Medical University, Tochigi Pediatric Medical Center, Tochigi, Japan.
Int J Pediatr Otorhinolaryngol. 2016 Dec;91:159-165. doi: 10.1016/j.ijporl.2016.10.029. Epub 2016 Oct 26.
To retrospectively evaluate the long-term results of surgery for retrograde bone work, using soft-wall reconstruction of the canal wall, for pediatric cholesteatoma.
We retrospectively evaluated a series of 25 consecutive ears of 24 patients who were ≤16 years of age. All children underwent cholesteatoma surgery between October 2002 and August 2008. The type of cholesteatoma, the length of follow-up, the incidence of residual and recurrent cholesteatoma, postoperative hearing results, and the form of the reconstructed external canal wall and tympanic membrane were assessed.
There were 21 males and 3 females. The procedure was performed on both ears of one patient who had bilateral congenital cholesteatoma (CC). At the initial surgery, 16 cases (64%) had CC and nine (36%) had acquired cholesteatoma (AC). The mean age at surgery was 8.2 years and 10.4 years for CC and AC cases, respectively. The mean postoperative follow-up period after the initial surgery was 90 months for CC cases and 108 months for AC cases. Cholesteatoma recurrence occurred for 6% and 56% of cases with CC and AC, respectively. Successful serviceable hearing was achieved for 93.8% with CC and 100% with AC. Cases with inadequate hearing after surgery were characterized by disease extension to the mastoid and the protympanum. The long-term forms of the reconstructed external canal wall changed depending on their middle ear aeration. Some cases of tympanic membrane perforation and otitis media with effusion were occurred during the follow-up period.
Overall, the retrograde approach with soft-wall reconstruction of the canal wall achieved a low recurrence rate for cholesteatoma and good hearing outcomes during long-term follow-up for the pediatric case. However, in cases with eustachian tube dysfunction and/or cholesteatoma involving the protympanum, the hearing outcomes were less favorable.
回顾性评估小儿胆脂瘤采用耳道壁软壁重建的逆行性骨质手术的长期效果。
我们回顾性评估了24例年龄≤16岁患者的25只连续耳朵。所有儿童在2002年10月至2008年8月期间接受了胆脂瘤手术。评估了胆脂瘤的类型、随访时间、残余和复发性胆脂瘤的发生率、术后听力结果以及重建外耳道壁和鼓膜的形态。
男性21例,女性3例。一名双侧先天性胆脂瘤(CC)患者的双耳均接受了该手术。初次手术时,16例(64%)为CC,9例(36%)为后天性胆脂瘤(AC)。CC和AC病例的平均手术年龄分别为8.2岁和10.4岁。CC病例初次手术后的平均术后随访期为90个月,AC病例为108个月。CC和AC病例的胆脂瘤复发率分别为6%和56%。CC患者的有效听力成功率为93.8%,AC患者为100%。术后听力不足的病例以疾病扩展至乳突和鼓室前部为特征。重建外耳道壁的长期形态根据中耳通气情况而变化。随访期间发生了一些鼓膜穿孔和中耳积液性中耳炎病例。
总体而言,采用耳道壁软壁重建的逆行性方法在小儿病例的长期随访中胆脂瘤复发率低,听力结果良好。然而,在咽鼓管功能障碍和/或胆脂瘤累及鼓室前部的病例中,听力结果不太理想。