Vashishth Ashish, Singh Nagar Tilak Raj, Mandal Shantanu, Venkatachalam Vellore Pattabhiram
Department of ENT and Head and Neck Surgery, Vardhaman Mahavir Medical College and Safdarjung Hospital, New Delhi, India,
Eur Arch Otorhinolaryngol. 2015 Feb;272(2):289-95. doi: 10.1007/s00405-013-2852-y. Epub 2013 Dec 8.
The purpose of the study was to review the clinical features, complications, surgical management and post-operative outcomes of medially invasive extensive cholesteatomas and intracranial complications of cholesteatoma. The retrospective review was carried out at a tertiary referral center and included 20 patients presenting with extensive intratemporal cholesteatomas between 2011 and 2013. Inclusion criteria were involvement of the labyrinth, facial nerve, posterior fossa dura and intracranial complications. The mean age of the patients was 20 years. Profuse foul-smelling otorrhoea and severe otalgia/temporal headache were the most common presenting features. Intracranial complications were observed in nine patients, most commonly temporal lobe abscess; 14/20 patients exhibited profound hearing loss. One case exhibited massive labyrinthine petrous apex cholesteatoma. Labyrinthine destruction was seen in all cases of facial nerve involvement. Management of intracranial complications preceded canal wall-down mastoidectomy with or without partial labyrinthectomy and subtotal petrosectomy (transotic) with blind sac closure for petrous cholesteatoma. Facial nerve infiltration was observed in one case, whereas eight cases exhibited gross dehiscence of the fallopian canal. Disease clearance was complete in all cases with two mortalities in patients with intracranial complications. Post-operative course was uncomplicated in all other patients apart from a case of wound dehiscence. All patients remain disease free after a minimum and maximum follow-up of 6 months and 2 years, respectively. Extensive intratemporal cholesteatomas and intracranial complications caused by them continue to pose a challenge to the management of otitis media in the current era and merit early recognition, surgical management and follow-up.
本研究的目的是回顾内侧侵袭性广泛性胆脂瘤及胆脂瘤颅内并发症的临床特征、并发症、手术治疗及术后结果。该回顾性研究在一家三级转诊中心开展,纳入了2011年至2013年间出现颞骨内广泛性胆脂瘤的20例患者。纳入标准为累及迷路、面神经、后颅窝硬脑膜及颅内并发症。患者的平均年龄为20岁。大量恶臭耳漏及严重耳痛/颞部头痛是最常见的临床表现。9例患者出现颅内并发症,最常见的是颞叶脓肿;20例患者中有14例表现为重度听力损失。1例出现巨大的岩尖迷路胆脂瘤。所有面神经受累病例均可见迷路破坏。颅内并发症的处理先于开放式乳突根治术(伴或不伴部分迷路切除术)及岩骨次全切除术(经耳道),并对岩部胆脂瘤行盲袋封闭术。1例观察到面神经浸润,而8例出现面神经管严重裂开。所有病例病变均完全清除,颅内并发症患者中有2例死亡。除1例伤口裂开外,所有其他患者术后病程均无并发症。所有患者在分别经过最短6个月、最长2年的随访后均无疾病复发。在当今时代,颞骨内广泛性胆脂瘤及其引起的颅内并发症对中耳炎的治疗仍然构成挑战,值得早期识别、手术治疗及随访。