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Effect of Bioabsorbable Poly (dl-Lactide ε-Caprolactone) on Healing of Experimentally Injured Acute Traumatic Middle Ear Mucosa Damage. 生物可吸收聚乳酸- ε-己内酯对实验性急性外伤性中耳黏膜损伤愈合的影响。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-06-01 DOI: 10.5152/iao.2023.22883
Necati İlhan, Ahmet Kara, Elvan Şahin, Mahmut Sinan Yılmaz, Mehmet Güven, Miyase Erdoğan, Deniz Demir

Background: Postoperative adhesion is an important complication after middle-ear surgeries. Although many materials have been tried to prevent this complication, the use of Poly (dl-lactide ε-caprolactone) as an anti-adhesive material after middle-ear surgery has not yet been reported. The aim of this study was to evaluate the anti-adhesive effect of poly (dl-lactide ε-caprolactone) on the ears of rats with middle-ear mucosa damage.

Methods: In our study, 14 Wistar albino rats and 28 ears in total were used. The rats were randomly divided into 4 groups. Middle ear mucosa damage was performed in all groups with a transcanal approach under otomicroscopy in sterile conditions. The effects of poly (dl-lactide ε-caprolactone), silicone sheet, and absorbable gelatin sponge were compared histologically with the secondary healing group. In addition, hearing evaluation was performed before the procedure and on the 28th postoperative day.

Results: No significant difference was observed in transient otoacoustic emission and distortion product otoacoustic emissions tests performed before and after the surgical procedure when the groups were compared. While adhesion was observed in the tympanic membrane in the absorbable gelatin sponge group, no adhesion was observed in the other groups. In the absorbable gelatin sponge group, increased fibroblastic activity, inflammation, and neovascularization were observed in the middle-ear mucosa. No significant difference was observed in silicone sheet, poly (dl-lactide ε-caprolactone), and control groups in terms of fibroblastic activity, inflammation, and neovascularization.

Conclusion: It can be concluded that absorbable poly (dl-lactide ε-caprolactone) is nonototoxic and biocompatible with the rat's middle ear cavity by short-term evaluation.

背景:术后粘连是中耳手术后的重要并发症。虽然许多材料已经尝试防止这种并发症,但在中耳手术后使用聚(dl-乳酸- ε-己内酯)作为抗粘连材料尚未见报道。本研究旨在探讨聚乳酸- ε-己内酯对中耳黏膜损伤大鼠的抗粘附作用。方法:选用Wistar白化大鼠14只,共28耳。将大鼠随机分为4组。所有组在无菌条件下经鼻入路耳镜下进行中耳粘膜损伤。与二次愈合组比较聚乳酸- ε-己内酯、硅胶片和可吸收明胶海绵的组织学效果。术前和术后第28天分别进行听力评估。结果:两组在手术前后进行的瞬态耳声发射和畸变产物耳声发射试验比较无显著差异。可吸收明胶海绵组鼓膜有粘连,其他组鼓膜无粘连。在可吸收明胶海绵组,观察到中耳粘膜纤维母细胞活性、炎症和新生血管的增加。硅胶片组、聚乳酸- ε-己内酯组和对照组在成纤维细胞活性、炎症和新生血管方面无显著差异。结论:经短期评价,可吸收聚乳酸- ε-己内酯无耳毒性,与大鼠中耳腔具有生物相容性。
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引用次数: 0
Is Facial Nerve Decompression Justified in Malignant External Otitis? Literature Review and Own Experience. 面神经减压治疗恶性外耳炎是否合理?文献综述与亲身体会。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-06-01 DOI: 10.5152/iao.2023.22892
Joanna Marszał, Małgorzata Wierzbicka, Anna Bartochowska

Objective: The aim of the study was to present the indications for facial nerve decompression in malignant external otitis, to analyze the results of such treatment, and to describe own experience in that field.

Methods: A search in the PubMed and Google Scholar databases for English language articles published between 1968 and May 2022 was performed. We focused on papers describing patients with malignant external otitis and facial nerve palsy treated by decompression. Moreover, retrospective analysis of 24 consecutive patients with malignant external otitis hospitalized in our department in the past 10 years was performed.

Results: In the literature, 48 cases with malignant external otitis and facial nerve paresis treated by decompression were identified. In total, 41 patients recovered (85.42%), 4 died (1 due to exacerbation of the disease, 2 for pneumonia, and 1 for heart failure), and in 3 cases the final outcome was not presented. In most cases (24; 50%), facial nerve function did not improve after decompression, in 8 patients (16.67%) partial recovery was observed, in 11 cases (22.92%) full improvement was observed, and data were not given for 5 patients. In only one case, the spread of infection and deterioration of local and general patient states were noted. In our material, we identified 13 patients with malignant external otitis and facial nerve palsy. Two of them were treated surgically, of which only one had facial nerve decompression. Partial improvement of facial nerve function was observed after 6 months of rehabilitation.

Conclusion: The management of malignant external otitis is still difficult and not well defined. Facial nerve decompression seems justified in selected cases of malignant external otitis not responding to conservative treatment.

目的:介绍恶性外耳炎面神经减压术的适应证,分析其治疗效果,并阐述自己的经验。方法:在PubMed和Google Scholar数据库中检索1968年至2022年5月间发表的英文文章。我们着重研究了用减压术治疗恶性外耳炎和面神经麻痹的病例。并对我科10年来连续住院的24例恶性外耳炎患者进行回顾性分析。结果:对48例经减压治疗的恶性外耳炎合并面神经麻痹患者进行了回顾性分析。共有41例患者康复(85.42%),4例死亡(1例因病情加重,2例因肺炎,1例因心力衰竭),3例未见最终结果。在大多数情况下(24;50%),减压后面神经功能未见改善,8例(16.67%)部分恢复,11例(22.92%)完全改善,5例未给出资料。只有一个病例,感染的传播和恶化的地方和一般病人的状态被注意到。在我们的资料中,我们确定了13例恶性外耳炎和面神经麻痹患者。其中2例采用手术治疗,其中1例采用面神经减压术。康复6个月后,面神经功能部分改善。结论:恶性外耳炎的治疗仍然困难且不明确。面神经减压似乎是合理的,在恶性外耳炎的情况下,不响应保守治疗。
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引用次数: 0
Expression and Correlation Research of MicroRNA10a-5p and PIK3CA in Middle Ear Cholesteatoma. MicroRNA10a-5p和PIK3CA在中耳胆脂瘤中的表达及相关性研究
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-06-01 DOI: 10.5152/iao.2023.22863
Jing Yang, Wei Yan, Susu Tang, Zhikun Huang, Mingyuan Ye, Zheng Lu, Qianxu Liu

Background: This study aimed to examine the roles of miR-10a-5p and phosphatidylinositol-4,5-bisphosphonate 3-kinase catalytic subunit α in the pathogenesis of middle ear cholesteatoma.

Methods: We enrolled 27 patients with middle ear cholesteatoma and collected samples of intraoperative cholesteatoma and normal posterior ear skin tissues. The mRNA expression levels of miR-10a-5p and PIK3CA were detected using real-time quantitative polymerase chain reaction. PIK3CA protein expression was measured by immunohistochemistry and western blotting.

Results: Middle ear cholesteatoma tissues showed significantly lower miR-10a-5p expression levels and significantly higher PIK3CA expression levels than normal posterior ear skin tissues (both P < .05). Furthermore, the miR-10a-5p and PIK3CA expression levels were significantly negatively correlated in middle ear cholesteatoma tissues (r = -0.926, P < .001).

Conclusion: Low miR-10a-5p expression levels in middle ear cholesteatoma tissues may inhibit the growth and proliferation of cholesteatoma, whereas high PIK3CA expression level may promote its growth and proliferation. In addition, miR-10a-5p may affect the proliferation and differentiation of cholesteatoma by negatively regulating its target gene, PIK3CA.

背景:本研究旨在探讨miR-10a-5p和磷脂酰肌醇-4,5-二膦酸盐3-激酶催化亚基α在中耳胆脂瘤发病机制中的作用。方法:选取27例中耳胆脂瘤患者,取术中胆脂瘤及正常后耳皮肤组织标本。采用实时定量聚合酶链反应检测miR-10a-5p和PIK3CA mRNA表达水平。免疫组织化学和western blotting检测PIK3CA蛋白表达。结果:中耳胆脂瘤组织miR-10a-5p表达水平明显低于后耳正常皮肤组织,PIK3CA表达水平明显高于后耳正常皮肤组织(P < 0.05)。miR-10a-5p与PIK3CA在中耳胆脂瘤组织中的表达水平呈显著负相关(r = -0.926, P < 0.001)。结论:中耳胆脂瘤组织中miR-10a-5p低表达可抑制胆脂瘤的生长和增殖,而PIK3CA高表达可促进其生长和增殖。此外,miR-10a-5p可能通过负调控其靶基因PIK3CA影响胆脂瘤的增殖和分化。
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引用次数: 1
Auditory Neuropathy Spectrum Disorder in the White Sutton Syndrome. 白萨顿综合征的听神经病变谱系障碍。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-06-01 DOI: 10.5152/iao.2023.22877
Lucia Belen Musumano, Virginia Fancello, Laura Negossi, Elisa Ballardini, Stefania Bigoni, Andrea Ciorba
White Sutton Syndrome is a rare autosomal dominant disorder resulting from a de novo mutation of Pogo Transposable Element Derived with Zinc Finger domain gene. The phenotype is characterized by a wide spectrum of cognitive dysfunction and developmental delays. Hearing loss is frequently mentioned as one of the symptoms of this rare disease, but details are usually scant. We report a case of a male child affected by White Sutton Syndrome and sensorineural hearing loss, with audiological findings of an auditory neuropathy spectrum disorder, a dysfunction of the auditory pathway with preserved cochlear outer hair cell function. Up to date, the present case is the first description of hearing loss due to an auditory neuropathy spectrum disorder in White Sutton Syndrome. A comprehensive audiological assessment is therefore mandatory in all White Sutton Syndrome patients in order to recognize a possible auditory neuropathy disorder and then avoid misdiagnosis, or erroneous clinical management.
白萨顿综合征是一种罕见的常染色体显性遗传病,由锌指结构域基因衍生的Pogo转座因子从头突变引起。该表型的特点是广泛的认知功能障碍和发育迟缓。听力损失经常被认为是这种罕见疾病的症状之一,但细节通常很少。我们报告一例男性儿童受怀特萨顿综合征和感音神经性听力损失的影响,听力学结果为听神经病变谱系障碍,听觉通路功能障碍,保留耳蜗外毛细胞功能。到目前为止,本病例是怀特萨顿综合征中听觉神经病变谱系障碍引起的听力损失的第一个描述。因此,对所有White Sutton综合征患者进行全面的听力学评估是强制性的,以便识别可能的听神经病变障碍,从而避免误诊或错误的临床处理。
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引用次数: 1
A De Novo Mutation in SOX10 in a Chinese Boy with Waardenburg Syndrome Type 2. 中国Waardenburg综合征2型男孩SOX10基因从头突变
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-06-01 DOI: 10.5152/iao.2023.22745
Min Guo, Qing Li, Chaowu Jiang, Shuling Li, Biao Ruan

Waardenburg syndrome is an autosomal dominant inherited syndromic hereditary hearing loss characterized by varying combinations of sensorineural hearing loss and abnormal pigmentation of the hair, skin, and inner ear. The aim of this study was to analyze the clinical phenotypes and genetic variants of a Chinese boy with Waardenburg syndrome type 2 and to explore the possible molecular pathogenesis of Waardenburg syndrome type 2. Clinical, audiological, and ophthalmologic evaluations were performed on the proband. Clinical data from the principal members in the proband's family were collected through questionnaires. Genetic analysis was conducted, including targeted next-generation sequencing of 144 known deafness genes, Sanger sequencing, and bioinformatic analysis. Waardenburg syndrome type 2was diagnosed in a 4-year-old boy according to the Waardenburg Syndrome Consortium Criteria. The novel missense mutation c.426G>T (p.Trp142Cys) was identified in SOX10 in the proband but was absent in his parents and the controls. A de novo missense mutation in SOX10 was the genetic cause of Waardenburg syndrome type 2 in the proband, which was useful for the molecular diagnosis of Waardenburg syndrome type 2.

Waardenburg综合征是一种常染色体显性遗传综合征遗传性听力损失,其特征是感觉神经性听力损失和头发、皮肤和内耳色素沉着异常的不同组合。本研究的目的是分析中国男孩Waardenburg综合征2型的临床表型和遗传变异,并探讨Waardenburg综合征2型可能的分子发病机制。对先证者进行临床、听力学和眼科评估。通过问卷调查收集先证者家庭主要成员的临床资料。进行遗传分析,包括144个已知耳聋基因的靶向下一代测序、Sanger测序和生物信息学分析。根据Waardenburg综合征联盟标准,诊断为一名4岁男孩Waardenburg综合征2型。在先证者SOX10中发现了新的错义突变c.426G>T (p.Trp142Cys),但在其父母和对照组中不存在。先证者SOX10从头错义突变是Waardenburg综合征2型的遗传原因,这对Waardenburg综合征2型的分子诊断有帮助。
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引用次数: 0
Universal Repositioning Maneuver: A New Treatment for Single Canal and Multi-Canal Benign Paroxysmal Positional Vertigo by 3-Dimensional Model Analysis. 通用复位手法:一种治疗单管和多管良性阵发性位置性眩晕的新方法。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-06-01 DOI: 10.5152/iao.2023.22921
Renato Gonzaga Barreto, Darío Andrés Yacovino, Marcello Cherchi, Lázaro Juliano Teixeira, Saulo Nardy Nader, Gabriel Freitas Leão

Background: Benign paroxysmal positional vertigo is the most common peripheral vestibular disorder and is currently treated by many types of repositioning maneuvers. A simplification of this procedure would be desirable. A new, anatomically realistic, 3-dimensional computational simulator of the human labyrinth provides a novel insight to evaluate the viability of any new maneuver. The purpose of this study is to propose a single maneuver with potential to treat canalolithiasis-type benign paroxysmal positional vertigo of any individual canal, or even multiple canals on the same side, based on a 3-dimensional model.

Methods: The benign paroxysmal positional vertigo Viewer, a 3-dimensional model of the human labyrinth, was used to analyze a "Universal Repositioning Maneuver."

Result: Through the gravity vector, the expected position of the otoliths was demonstrated by moving the model through a single sequence of head positions, successfully promoting otolith migration from the three semicircular canals to the utricular cavity, either individually or together.

Conclusion: The analysis with the 3-dimensional model predicts the effectiveness of the Universal Repositioning Maneuver for the resolution of each single canal or multiple-canal benign paroxysmal positional vertigo canalolithiasis, making treatment much more straightforward.

背景:良性阵发性位置性眩晕是最常见的外周前庭功能障碍,目前可通过多种复位手法治疗。简化这一程序是可取的。一个新的,解剖学上真实的,人类迷宫的三维计算模拟器提供了一个新的见解,以评估任何新的操作的可行性。本研究的目的是提出一种基于三维模型的单一操作方法,可以治疗任何单个椎管结石型良性阵发性位置性眩晕,甚至是同一侧的多个椎管。方法:采用良性阵发性位置性眩晕三维模型Viewer对人体迷宫的“通用重定位操作”进行分析。结果:通过重力矢量,通过单个头部位置序列移动模型来显示耳石的预期位置,成功地促进了耳石从三个半规管向室腔的移动,无论是单独的还是一起的。结论:三维模型分析预测了通用复位手法对单管或多管良性阵发性体位性眩晕管结石的治疗效果,使治疗更加简单。
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引用次数: 1
A Computer Vision Algorithm to Classify Pneumatization of the Mastoid Process on Temporal Bone Computed Tomography Scans. 颞骨计算机断层扫描乳突突气肿分类的计算机视觉算法。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-06-01 DOI: 10.5152/iao.2023.22958
Zubair Hasan, Michael Lee, Fiona Chen, Seraphina Key, Al-Rahim Habib, Layal Aweidah, Raymond Sacks, Narinder Singh

Background: Pneumatization of the mastoid process is variable and of significance to the operative surgeon. Surgical approaches to the temporal bone require an understanding of pneumatization and its implications for surgical access. This study aims to determine the feasibility of using deep learning convolutional neural network algorithms to classify pneumatization of the mastoid process.

Methods: De-identified petrous temporal bone images were acquired from a tertiary hospital radiology picture archiving and communication system. A binary classification mode in the pretrained convolutional neural network was used to investigate the utility of convolutional neural networks in temporal bone imaging. False positive and negative images were reanalyzed by the investigators and qualitatively assessed to consider reasons for inaccuracy.

Results: The overall accuracy of the model was 0.954. At a probability threshold of 65%, the sensitivity of the model was 0.860 (95% CI 0.783-0.934) and the specificity was 0.989 (95% CI 0.960-0.999). The positive predictive value was 0.973 (95% CI 0.904-0.993) and the negative predictive value was 0.935 (95% CI 0.901-0.965). The false positive rate was 0.006. The F1 number was 0.926 demonstrating a high accuracy for the model.

Conclusion: The temporal bone is a complex anatomical region of interest to otolaryngologists. Surgical planning requires high-resolution computed tomography scans, the interpretation of which can be augmented with machine learning. This initial study demonstrates the feasibility of utilizing machine learning algorithms to discriminate anatomical variation with a high degree of accuracy. It is hoped this will lead to further investigation regarding more complex anatomical structures in the temporal bone.

背景:乳突气化是可变的,对外科医生有重要意义。颞骨的手术入路需要了解气动及其对手术入路的影响。本研究旨在确定使用深度学习卷积神经网络算法对乳突气化进行分类的可行性。方法:从某三级医院放射影像档案及通讯系统中获取去识别的颞骨岩质图像。采用预训练卷积神经网络中的二值分类模式,研究了卷积神经网络在颞骨成像中的应用。假阳性和阴性图像由调查人员重新分析和定性评估,以考虑不准确的原因。结果:模型的总体准确度为0.954。在65%的概率阈值下,模型的敏感性为0.860 (95% CI 0.783-0.934),特异性为0.989 (95% CI 0.960-0.999)。阳性预测值为0.973 (95% CI 0.904 ~ 0.993),阴性预测值为0.935 (95% CI 0.901 ~ 0.965)。假阳性率为0.006。F1值为0.926,表明模型具有较高的精度。结论:颞骨是耳鼻喉科医师感兴趣的复杂解剖区域。手术计划需要高分辨率的计算机断层扫描,机器学习可以增强对其的解释。这项初步研究证明了利用机器学习算法以高精度区分解剖变异的可行性。希望这将导致对颞骨更复杂解剖结构的进一步研究。
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引用次数: 0
Surgical Management of Endolymphatic Sac Tumor: A Systematic Review and Meta-Analysis. 内淋巴囊瘤的外科治疗:系统回顾和荟萃分析。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-06-01 DOI: 10.5152/iao.2023.22957
Federico Maria Gioacchini, Giuseppe Chiarella, Shaniko Kaleci, Giannicola Iannella, Pasquale Viola, Davide Pisani, Alfonso Scarpa, Michele Tulli, Massimo Re

The aim of our study was to report rates of facial nerve palsy and residual tumor following surgical intervention and subsequent tumor recurrence in patients with endolymphatic sac tumors. A systematic literature review of preoperative assessment and surgical management is also included. Studies including patient/s affected by sporadic or von Hippel-Lindau disease related endolymphatic sac tumors, reporting levels of facial nerve function, residual and recurrence pathology following a surgical procedure, were considered. Data were combined for proportional meta-analysis, and the selected studies' methodological quality was also evaluated. Overall 34 papers, including 202 subjects (209 cases of endolymphatic sac tumors) were analyzed. Pooled proportion rate (95% CI) of overall facial nerve palsy was 39.7% (28.2-51.9) and residual tumor was 16.5% (10.3-23.7) after surgical procedure. Pooled proportion rate (95% CI) of tumor recurrence was 14.0% (9.7-19.3) during a mean follow-up period of 49.7 months (8-136). Our results showed that preoperative facial nerve function is impaired in almost 30% of patients with endolymphatic sac tumors. Surgical management of endolymphatic sac tumor may cause a worsening of facial nerve function in a low percentage of treated subjects. Residual and/or recurrence of endolymphatic sac tumors are not rare events, and follow-up strategies should be designed accordingly.

我们研究的目的是报告手术后面神经麻痹和残留肿瘤的发生率以及内淋巴囊肿瘤患者随后的肿瘤复发率。系统的文献回顾术前评估和手术处理也包括在内。研究包括散发性或希佩尔-林道病相关的内淋巴囊肿瘤患者,报告面神经功能水平,手术后的残留和复发病理。将数据合并进行比例荟萃分析,并对所选研究的方法学质量进行评估。共分析34篇,202例(209例内淋巴囊肿瘤)。术后整体面神经麻痹合并比例(95% CI)为39.7%(28.2 ~ 51.9),残留肿瘤为16.5%(10.3 ~ 23.7)。在平均49.7个月(8-136)的随访期间,肿瘤复发率(95% CI)为14.0%(9.7-19.3)。我们的研究结果显示,近30%的内淋巴囊肿瘤患者术前面神经功能受损。内淋巴囊肿瘤的手术治疗可能导致面神经功能的恶化,在一个低百分比的治疗对象。内淋巴囊肿瘤的残留和/或复发并不罕见,因此应设计相应的随访策略。
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引用次数: 0
A Bilateral Vestibular Schwannoma is Not Always Related to Neurofibromatosis Type 2. 双侧前庭神经鞘瘤并不总是与2型神经纤维瘤病有关。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-06-01 DOI: 10.5152/iao.2023.22922
Andi Abeshi, Gian Gaetano Ferri

Bilateral vestibular schwannomas are commonly diagnosed in patients affected by neurofibromatosis type 2, a genetic disease caused by a heterozygous mutation in the gene region encoding neurofibromin-2. Sporadic bilateral vestibular schwannomas are very rare entities affecting almost exclusively elderly people. We present the case of a senior woman who was followed up with the "wait-and-scan" strategy for a unilateral vestibular schwannoma that later developed as a contralateral tumor, compatible with vestibular schwannoma, raising questions about its nature and risk of having been transmitted in offspring. Genetic testing excluded mutations of the neurofibromatosis type 2 gene. The presence of bilateral vestibular schwannomas is often considered pathognomonic of neurofibromatosis type 2, but the estimated probability of sporadic bilateral tumors in the absence of other neurofibromatosis type 2 features is 50% over 70 years of age. Therefore, the NF2 gene assessment is in any case recommended in these patients not only for an evaluation of the risk of being transmitted. The treatment strategy should be carefully personalized for each patient, considering the size of the tumors, symptoms, and hearing function together with the patient's age.

双侧前庭神经鞘瘤通常在2型神经纤维瘤病患者中诊断出来,2型神经纤维瘤病是一种由编码神经纤维蛋白-2基因区域的杂合突变引起的遗传性疾病。散发性双侧前庭神经鞘瘤非常罕见,几乎只影响老年人。我们报告了一位老年女性的病例,她的单侧前庭神经鞘瘤后来发展为对侧肿瘤,与前庭神经鞘瘤相容,对其性质和遗传给后代的风险提出了疑问。基因检测排除了2型神经纤维瘤病基因突变。双侧前庭神经鞘瘤的存在通常被认为是2型神经纤维瘤病的典型症状,但在没有其他2型神经纤维瘤病特征的情况下,估计70岁以上患者出现散发双侧肿瘤的概率为50%。因此,无论如何,推荐在这些患者中进行NF2基因评估,不仅是为了评估被传播的风险。考虑到肿瘤的大小、症状、听力功能以及患者的年龄,治疗策略应针对每位患者进行仔细的个性化治疗。
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引用次数: 0
Indications of and Efficacy of Facial Nerve Decompression Through Endoscopic Transcanal Approach for Patients with Traumatic Facial Paralysis. 经鼻内镜下面神经减压术治疗外伤性面瘫的适应证及疗效观察。
IF 1 4区 医学 Q3 Medicine Pub Date : 2023-06-01 DOI: 10.5152/iao.2023.22924
Wenying Shu, Lu Xue, Yaoxuan Wang, Zhaoyan Wang

Background: The aim of this study is to evaluate the indications and efficacy of facial nerve decompression through an endoscopic transcanal approach for patients with traumatic facial paralysis.

Methods: This single-center retrospective study included 11 patients with traumatic facial paralysis from February 2018 to April 2019. We compared the facial nerve and auditory function before and after operation so as to reveal the feasibility and effect of the surgical approach.

Results: All 11 patients have successfully received facial nerve decompression through endoscopic transcanal approach. Facial nerve function was objectively evaluated by electroneurography test and House-Brackmann facial nerve grading system. All patients were graded HB-VI with electroneurography ≥ 95% before surgery. The recovery of facial nerve function was good (HB-I or II) (90.9%) a year after surgery with only one case (9.1%) for HB-III. Preoperative high-resolution computed tomography showed that 1 patient had ossicular chain interruption, which was confirmed during operation. Meanwhile, 2 patients with air-bone gap >35 dBHL and whose computed tomography failed to diagnose were found with ossicular chain interruption during operation. The air-bone gap of patients with normal ossicular chain connection was all <30 dBHL. The average air-bone gap was reduced from 27.5 ± 10.1 dBHL to 7.8 ± 3.3 dBHL after operation.

Conclusion: Preoperative high-resolution computed tomography combined with localization test can accurately estimate the location of facial nerve injury. Facial nerve decompression through endoscopic transcanal approach can decompress the geniculate ganglion to pyramidal segment of facial nerve, which is suitable for patients with traumatic facial paralysis of this segment. In addition, air-bone gap >35 dBHL may indicate the ossicular chain interruption when it is difficult to be completely judged by high-resolution computed tomography.

背景:本研究旨在探讨经鼻内镜下面神经减压术治疗外伤性面瘫的适应症和疗效。方法:本研究为单中心回顾性研究,纳入2018年2月至2019年4月11例外伤性面瘫患者。通过对手术前后面神经和听觉功能的比较,揭示手术入路的可行性和效果。结果:11例患者均成功行经鼻内镜入路面神经减压术。采用神经电图测试和House-Brackmann面神经分级系统对面神经功能进行客观评价。所有患者术前神经电图评分为HB-VI级,≥95%。术后1年面神经功能恢复良好(HB-I或II) (90.9%), HB-III仅1例(9.1%)。术前高分辨率计算机断层扫描显示1例患者有听骨链中断,术中证实。同时,2例气骨间隙>35 dBHL且计算机断层扫描未能诊断的患者术中发现听骨链中断。结论:术前高分辨率计算机断层扫描结合定位试验可准确判断面神经损伤部位。内窥镜经扫描入路面神经减压可将膝状神经节减压至面神经锥体节段,适用于该节段外伤性面瘫患者。此外,当高分辨率计算机断层扫描难以完全判断时,气骨间隙>35 dBHL可能提示听骨链中断。
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Journal of International Advanced Otology
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