Butman John A, Kim H Jeffrey, Baggenstos Martin, Ammerman Joshua M, Dambrosia James, Patsalides Athos, Patronas Nicholas J, Oldfield Edward H, Lonser Russell R
Diagnostic Radiology Department, The Clinical Center of the National Institutes of Health, Bethesda, MD 20892, USA.
JAMA. 2007 Jul 4;298(1):41-8. doi: 10.1001/jama.298.1.41.
Endolymphatic sac tumors (ELSTs) are associated with von Hippel-Lindau disease and cause irreversible sensorineural hearing loss (SNHL) and vestibulopathy. The underlying mechanisms of audiovestibular morbidity remain unclear and optimal timing of treatment is not known.
To define the mechanisms underlying audiovestibular pathophysiology associated with ELSTs.
DESIGN, SETTING, AND PATIENTS: Prospective and serial evaluation of patients with von Hippel-Lindau disease and ELSTs at the National Institutes of Health between May 1990 and December 2006.
Clinical findings and audiologic data were correlated with serial magnetic resonance imaging and computed tomography imaging studies to determine mechanisms underlying audiovestibular dysfunction.
Thirty-five patients with von Hippel-Lindau disease and ELSTs in 38 ears (3 bilateral ELSTs) were identified. Tumor invasion of the otic capsule was associated with larger tumors (P = .01) and occurred in 7 ears (18%) causing SNHL (100%). No evidence of otic capsule invasion was present in the remaining 31 ears (82%). SNHL developed in 27 of these 31 ears (87%) either suddenly (14 ears; 52%) or gradually (13 ears; 48%) and 4 ears had normal hearing. Intralabyrinthine hemorrhage was found in 11 of 14 ears with sudden SNHL (79%; P < .001) but occurred in none of the 17 ears with gradual SNHL or normal hearing. Tumor size was not related to SNHL (P = .23) or vestibulopathy (P = .83).
ELST-associated SNHL and vestibulopathy may occur suddenly due to tumor-associated intralabyrinthine hemorrhage, or insidiously, consistent with endolymphatic hydrops. Both of these pathophysiologic mechanisms occur with small tumors that are not associated with otic capsule invasion.
内淋巴囊肿瘤(ELSTs)与冯·希佩尔-林道病相关,可导致不可逆的感音神经性听力损失(SNHL)和前庭病变。听觉前庭疾病的潜在机制尚不清楚,最佳治疗时机也未知。
明确与ELSTs相关的听觉前庭病理生理学的潜在机制。
设计、地点和患者:1990年5月至2006年12月在美国国立卫生研究院对冯·希佩尔-林道病和ELSTs患者进行前瞻性和系列评估。
将临床发现和听力学数据与系列磁共振成像和计算机断层扫描成像研究相关联,以确定听觉前庭功能障碍的潜在机制。
共识别出35例患有冯·希佩尔-林道病和ELSTs的患者,累及38只耳(3例双侧ELSTs)。肿瘤侵犯内耳囊与较大肿瘤相关(P = 0.01),7只耳(18%)发生侵犯,均导致SNHL(100%)。其余31只耳(82%)未发现内耳囊侵犯证据。这31只耳中有27只(87%)出现SNHL,其中14只(52%)突然发生,13只(48%)逐渐发生,4只耳听力正常。14只突然发生SNHL的耳中有11只(79%)发现迷路内出血(P < 0.001),而17只逐渐发生SNHL或听力正常的耳中均未出现。肿瘤大小与SNHL(P = 0.23)或前庭病变(P = 0.83)无关。
ELSTs相关的SNHL和前庭病变可能因肿瘤相关的迷路内出血突然发生,或隐匿发生,与内淋巴积水一致。这两种病理生理机制均发生于未侵犯内耳囊的小肿瘤。