Magliulo G, Terranova G, Sepe C, Cordeschi S, Cristofar P
Fourth ENT Department, University la Sapienza, Rome, Italy.
Clin Otolaryngol Allied Sci. 1998 Jun;23(3):253-8. doi: 10.1046/j.1365-2273.1998.00144.x.
This paper describes a series of patients with a petrous temporal bone cholesteatoma paying particular attention to the complications and their management. Sixteen patients who underwent surgery in our department were reviewed. Topographically, the petrous bone cholesteatomas were grouped into five categories according to the classification proposed by Sanna et al. There were five massive labyrinthine; five infralabyrinthine; one apical; four supralabyrinthine; and one infralabyrinthine-apical. Clinically, the presenting symptom of these lesions were facial nerve paralysis (10 patients) and unilateral deafness (13 patients). Total removal of the cholesteatomas was achieved in all patients using different surgical approaches according to their site and extent. Recurrences were observed in two patients after 8 months and 24 months, respectively. The facial nerve was infiltrated and compressed by the cholesteatoma in eight patients. Seven were managed with cable grafts using sural nerve. One of these patients was treated using a facial-hypoglossal anastomosis because of the failure of the graft. In the remaining patient, a baby-sitter procedure was employed. In the other two patients, the preoperative facial paralysis was due to compression by the cholesteatoma, and its removal allowed partial recovery of facial function. The rationale of the surgical management of petrous bone cholesteatoma is its radical and total removal. Our present policy is to prefer approaches which result in a closed cavity obliterating the eustachian tube and closing the auditory canal as a blind sac. Facial nerve function is the main complication of these lesions, Facial nerve involvement requires rapid management because the duration of the paralysis is directly related to poor recovery of facial function.
本文描述了一系列岩部颞骨胆脂瘤患者,特别关注其并发症及其处理。回顾了在我科接受手术的16例患者。从解剖学角度,根据Sanna等人提出的分类方法,岩部胆脂瘤分为五类。其中有5例巨大迷路型;5例迷路下型;1例岩尖型;4例迷路上型;1例迷路下 - 岩尖型。临床上,这些病变的主要症状为面神经麻痹(10例患者)和单侧耳聋(13例患者)。根据胆脂瘤的部位和范围,采用不同的手术入路,所有患者均实现了胆脂瘤的完全切除。分别在8个月和24个月后观察到2例患者复发。8例患者的面神经被胆脂瘤浸润和压迫。其中7例采用腓肠神经电缆移植治疗。由于移植失败,其中1例患者采用面神经 - 舌下神经吻合术治疗。在其余1例患者中,采用了保姆手术。另外2例患者术前面神经麻痹是由胆脂瘤压迫所致,切除胆脂瘤后,面神经功能部分恢复。岩部胆脂瘤手术治疗的原则是彻底完全切除。我们目前的策略倾向于采用能形成封闭腔隙、闭塞咽鼓管并将外耳道封闭成盲囊的入路。面神经功能是这些病变的主要并发症,面神经受累需要迅速处理,因为面神经麻痹的持续时间与面神经功能恢复不良直接相关。