Ungar Omer J, Franck Madeline, Nadol Joseph B, Santos Felipe
Department of Otolaryngology-Head and Neck Surgery.
Department of Maxillofacial Surgery, Tel Aviv Sourasky Medical Center, Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Laryngoscope. 2019 Jul;129(7):1667-1674. doi: 10.1002/lary.27601. Epub 2018 Dec 8.
OBJECTIVES/HYPOTHESIS: To describe the histopathologic findings and clinical presentation of arachnoid cysts (ACs) within the human temporal bone.
Retrospective cohort analysis.
An analysis of all medical records of patients diagnosed with an AC was performed. Temporal bones underwent standard processing for histologic examination. The slides were examined by light microscopy. The histologic findings were compared to premortem clinical data.
Twenty-seven ACs were identified in 22 patients. Twenty ears (74%) had no identified risk factor for AC development. The median volume was 12.8 mm . The most prevalent location of the ACs was at the fundus (16 ACs) followed by the middle portion of the internal auditory canal (IAC) (six ACs). Nine ACs were asymptomatic. Among the 18 symptomatic ACs, the most common presentation was sensorineural hearing loss (SNHL) (94%), followed by tinnitus (22%). The most affected structure was the cochlear nerve (59%), followed by the vestibular nerve (41%). The average hearing threshold was of moderately severe SNHL and speech discrimination was in the range of 50% on monosyllabic word tests. The median time interval from initial presentation to death was 12 years. No correlation was found between duration of symptoms and AC volume.
AC of the IAC is not uncommon. Its presentation is variable, ranging from asymptomatic to SNHL, with poor speech discrimination, tinnitus, and vertigo. This diagnosis should be kept in the differential diagnosis of retrocochlear pathologies.
4 Laryngoscope, 129:1667-1674, 2019.
目的/假设:描述人类颞骨内蛛网膜囊肿(ACs)的组织病理学发现和临床表现。
回顾性队列分析。
对所有诊断为AC的患者的医疗记录进行分析。颞骨经过标准处理用于组织学检查。切片通过光学显微镜检查。将组织学发现与生前临床数据进行比较。
在22例患者中发现了27个AC。20只耳朵(74%)未发现AC发生的危险因素。中位体积为12.8立方毫米。AC最常见的位置是在底部(16个AC),其次是内耳道(IAC)中部(6个AC)。9个AC无症状。在18个有症状的AC中,最常见的表现是感音神经性听力损失(SNHL)(94%),其次是耳鸣(22%)。受影响最严重的结构是蜗神经(59%),其次是前庭神经(41%)。平均听力阈值为中度重度SNHL,单音节词测试中的言语辨别率在50%范围内。从初次出现症状到死亡的中位时间间隔为12年。未发现症状持续时间与AC体积之间存在相关性。
IAC的AC并不罕见。其表现多样,从无症状到SNHL,伴有言语辨别能力差、耳鸣和眩晕。在蜗后病变的鉴别诊断中应考虑这一诊断。
4 喉镜,129:1667 - 1674,2019年。