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Epidemiology of common allergic diseases in China: Current position and implications 中国常见变态反应性疾病的流行病学现状及启示
Pub Date : 2025-06-04 DOI: 10.1002/eer3.70016
Xu Xu, Chengshuo Wang, Luo Zhang, Jingyun Li, Yuan Zhang

The prevalence of common allergic diseases, including allergic rhinitis, asthma, atopic dermatitis, and food allergy, has increased dramatically with rising industrialization in China, leading to a significant socio-economic burden. These allergic diseases are complex disorders influenced by both environmental and genetic factors. Epidemiological evidence indicates a parallel increase in the prevalence of other systemic diseases during the same period as the allergic disease epidemic, suggesting that these conditions may share common genetic mechanisms and potentially have a causal relationship. This review summarizes recent epidemiological studies on common allergic diseases in China, highlighting interrelated changes in demography, allergen spectrum, and the environmental and genetic implications. It aims to enhance our understanding of these conditions, contributing to the development of a robust public health monitoring network and the exploration of strategies for the prevention, control, and treatment of common allergic diseases in the Chinese population.

随着中国工业化程度的提高,包括变应性鼻炎、哮喘、特应性皮炎和食物过敏在内的常见变应性疾病的患病率急剧上升,导致了严重的社会经济负担。这些过敏性疾病是受环境和遗传因素影响的复杂疾病。流行病学证据表明,在过敏性疾病流行的同一时期,其他全身性疾病的患病率也在平行增加,这表明这些疾病可能具有共同的遗传机制,并可能存在因果关系。本文综述了近年来中国常见变态反应性疾病的流行病学研究,重点介绍了人口统计学、过敏原谱以及环境和遗传意义方面的相关变化。本研究旨在提高我们对这些疾病的认识,为建立健全的公共卫生监测网络和探索预防、控制和治疗中国人群常见过敏性疾病的策略做出贡献。
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引用次数: 0
Glioblastoma multiforme with transdural extension to the external auditory canal via the tegmen tympani—Clinical report with review of the literature 多形性胶质母细胞瘤经鼓膜经硬膜延伸至外耳道-临床报告并文献复习
Pub Date : 2025-04-23 DOI: 10.1002/eer3.70015
Arba Cecia, Emal Lesha, David G. Laird, Elsa Nico, Kaan Yagmurlu, Bruce L. Fetterman, L. Madison Michael II
<p>Glioblastoma multiforme (GBM) is the most aggressive and invasive malignant glioma, accounting for 45.2% of all cases with an annual incidence of 3.19 cases per 100,000 individuals and a median survival of 15 months [<span>1</span>]. Transdural extension of GBM is rare, particularly without previous surgical intervention [<span>2</span>]. Few reports have described cases of GBM propagating through the skull base [<span>3</span>]. Here, we report a case of a patient presenting with a temporal lobe GBM extending to the external auditory canal (EAC) through the tegmen tympani.</p><p>This case is reported as a descriptive study of a 60-year-old female with an extradural GBM. A literature review of the phenomenon was conducted and reported. This study was executed with ethical considerations, including informed consent. The participant provided consent after receiving an explanation of the procedures, potential risks and benefits, and right to withdraw.</p><p>A 60-year-old female with a history of Eustachian tube dysfunction presented with right ear otorrhea for several months. She required insertion of multiple tympanostomy tubes for the Eustachian tube dysfunction previously. Physical examination revealed decreased right-sided hearing, a 10% tympanic membrane perforation, local erythema, and serous fluid accumulation with a clear and normal EAC. She was prescribed antibiotics and scheduled for follow-up with audiometry results. In the interim, she developed bloody right ear drainage. A friable, smooth, vascular lesion obscuring the right ear’s EAC was discovered, biopsied, and returned as GBM.</p><p>A CT brain demonstrated a 2.5 cm temporal lobe mass with midline shift and vasogenic edema. Dehiscence of the right tegmen tympani was noted with abnormal soft tissue density throughout the right EAC, middle ear, and mastoid cells. MRI brain revealed a right temporal lobe mass with peripheral enhancement, central necrosis and vasogenic edema (Figure 1). There was contiguous enhancement in the right temporal bone and middle ear cavity, extending laterally towards the EAC and anteromedially towards the Eustachian tube.</p><p>The patient underwent resection via a combined approach. The surgery involved excision of the tumor from right EAC with middle ear exploration and tympanomastoidectomy. The tumor caused erosion of the incus and involved sectioning of the chorda tympani nerve. The following step included an infratemporal approach to the middle fossa and temporal lobe. Elevation of the dura revealed a subtemporal dural defect with tumor extending through the tegmen tympani into the middle ear without involvement of the Eustachian tube. The tumor in the middle ear, dura, and temporal lobe was resected, achieving gross total resection. Initial histopathology revealed hypercellularity, nuclear atypia, and necrosis concerning for high grade glioma (Figure 2). Pathology was significant for IDH1-wildtype GBM, WHO grade IV with KRAS mutation, PTEN mutation w
多形性胶质母细胞瘤(GBM)是最具侵袭性和侵袭性的恶性胶质瘤,占所有病例的45.2%,年发病率为3.19例/ 10万人,中位生存期为15个月。GBM经硬膜延伸是罕见的,特别是没有手术干预。很少有报道描述了GBM通过颅底[3]传播的病例。在此,我们报告一例患者表现为颞叶GBM通过鼓膜延伸到外耳道(EAC)。本病例报告为一60岁女性硬膜外GBM的描述性研究。对这一现象进行了文献综述并进行了报道。本研究是在伦理考虑下进行的,包括知情同意。参与者在接受了程序、潜在风险和利益以及退出权的解释后表示同意。60岁女性,有咽鼓管功能障碍病史,右耳耳漏数月。她之前因耳咽管功能障碍需要植入多根鼓膜造瘘管。体格检查显示右侧听力下降,10%鼓膜穿孔,局部红斑,浆液积聚,EAC清晰正常。医生给她开了抗生素,并安排了听力学结果的随访。在此期间,她出现右耳出血。发现一易碎、光滑的血管性病变,遮蔽了右耳EAC,活检后发现为GBM。脑部CT显示2.5 cm颞叶肿块伴中线移位及血管源性水肿。右侧鼓室被膜开裂,右耳门、中耳及乳突细胞内软组织密度异常。脑MRI显示右侧颞叶肿块伴周围强化、中央坏死和血管源性水肿(图1)。右侧颞骨和中耳腔连续强化,向外侧延伸至耳咽管,向前内侧延伸至耳咽管。患者经联合手术切除。手术包括右耳前耳区肿瘤切除、中耳探查及鼓膜瘤切除。肿瘤导致砧骨糜烂,并累及鼓室索神经的切面。接下来的步骤包括颞下入路到中窝和颞叶。硬脑膜抬高显示颞骨下硬脑膜缺损,肿瘤通过鼓膜延伸至中耳,但未累及咽鼓管。切除中耳、硬脑膜、颞叶肿瘤,实现大体全切除。最初的组织病理学显示高级别胶质瘤的高细胞、核异型性和坏死(图2)。idh1野生型GBM、WHOⅳ级KRAS突变、PTEN突变杂合性缺失、CDKN2A纯合性缺失和TERT启动子突变、G1/EGFR分子亚组病理差异显著。在一个不起眼的术后过程后,她接受了30次剂量为60 Gy的外部放射治疗,利用调强放射治疗和每日图像引导。该治疗后休息1个月,然后每天给予替莫唑胺和肿瘤治疗剂维持治疗6个月。在诊断后17个月的随访中,患者神经功能完好,听力改善,无复发迹象(图1)。在20个月的随访中,MRI成像显示她的胼胝体和中线结构的GBM复发无法手术。她出现了短期记忆问题,但在最后一次随访中,自最初诊断29个月以来,仍在维持替莫唑胺和肿瘤治疗领域。GBM经颅底的硬膜延伸是罕见的,文献报道很少,这是第三例报道的病例[3]。虽然GBM神经外扩散的病理生理机制尚不清楚,但外科手术可通过破坏血管和血脑屏障加速这种传播[4,5]。其他因素如高血压引起的硬脑膜和中窝和颅底孔的血管裂缝可传播GBM[4]的扩散。鼓膜是颞骨岩部的低阻力板,将颅内间隙与中耳区隔开。这个独特的病例涉及由肿瘤从颞叶通过EAC突出到颞骨引起的鼓室被裂。裂裂可能是由于肿瘤浸润导致颅内压升高,并与脑脊液(CSF)泄漏[6]有关。脑脊液减少会减少脑缓冲,使特定骨区域的脑搏动,导致骨重塑和肿瘤浸润。据Belal等人报道,转移到鼓膜本身。 ,评估颞骨转移性病变,报告鼓室盖是第二常见的转移部位。虽然该患者有多次鼓室造瘘置管和耳咽管功能障碍的病史,但复发的置管不太可能导致被盖缺损导致GBM扩展到EAC。文献回顾发现两例GBM通过被盖延伸至颅外腔室的报道(表1)。Nager等人报道了一名41岁的患者,其表现为右侧EAC突出肿块,表现为右侧额颞部GBM穿过被膜并突出穿过鼓膜进入右侧EAC[2]。Thrull等人报道了一名61岁的患者,表现为左侧偏瘫和右侧听力受损,影像学显示右侧颞叶肿块通过乳突被盖浸润颞骨,进入乳突细胞。经颞开颅切除肿瘤,最终病理符合GBM IDH-1野生型,MGMT甲基化[3]。Arba Cecia:概念化;正式的分析;方法;验证;可视化;原创作品草案;写作-审查和编辑。Emal Lesha:概念化;数据管理;调查;方法;监督;原创作品草案;写作-审查和编辑。David G. Laird:数据管理;正式的分析;方法;验证;可视化;原创作品草案;写作-审查和编辑。Elsa Nico:数据管理;正式的分析;调查;验证;可视化;原创作品草案;写作-审查和编辑。Kaan Yagmurlu:概念化;调查;方法;监督;验证;可视化;原创作品草案;写作-审查和编辑。Bruce L. Fetterman:概念化;调查;方法;资源;原创作品草案;写作-审查和编辑。L.麦迪逊·迈克尔二世:概念化;方法;项目管理;资源;监督;验证;可视化;原创作品草案;写作-审查和编辑。获得了所有参与者的知情同意。作者声明无利益冲突。鉴于本案例研究的性质,不需要IRB批准。这项工作的创作严格遵循了该机构的所有道德标准。
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引用次数: 0
Activation and inhibition of Notch signaling facilitate proliferative regeneration of sensory cells in adult mice Notch信号的激活和抑制促进了成年小鼠感觉细胞的增殖再生
Pub Date : 2025-04-23 DOI: 10.1002/eer3.70008
Shan Zeng, Tao Jiang, Zhengyi Chen, Huawei Li, Luo Guo, Wenyan Li

Due to the limited regenerative capacity in adult mammals, the loss of vestibular hair cells (HCs) leads to balance disorders. In this study, we chronologically reprogrammed adult vestibular supporting cells (SCs) via bimodal regulation of Notch signaling, mimicking dynamic changes in Notch signaling during inner ear development. We found that activating Notch signaling stimulated SC proliferation in damaged adult utricles, priming these cells with the potential to regenerate sensory HCs. Subsequent inhibition of Notch signaling removed lateral inhibition barriers, promoting the transition from proliferating SCs to HCs. Our findings underscore the crucial role of Notch signaling in promoting vestibular HC regeneration.

由于成年哺乳动物的再生能力有限,前庭毛细胞(hc)的损失导致平衡障碍。在这项研究中,我们通过Notch信号的双峰调节,按时间顺序对成人前庭支持细胞(SCs)进行了重编程,模拟了内耳发育过程中Notch信号的动态变化。我们发现,激活Notch信号可以刺激受损成人胞室中的SC增殖,使这些细胞具有再生感觉hc的潜力。随后对Notch信号的抑制消除了横向抑制屏障,促进了从增殖的SCs向hcc的转变。我们的发现强调了Notch信号在促进前庭HC再生中的关键作用。
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引用次数: 0
A one-year efficacy assessment of subcutaneous immunotherapy in dust mite allergic rhinitis patients based on clinical symptoms and objective biomarkers 基于临床症状和客观生物标志物的尘螨变应性鼻炎患者皮下免疫治疗一年疗效评估
Pub Date : 2025-04-23 DOI: 10.1002/eer3.70013
Jingwen Wang, Xu Xu, Xu Zhang, Yuan Zhang, Jingyun Li

Objective

To evaluate the 1-year efficacy of subcutaneous immunotherapy (SCIT) in treating dust mite-induced allergic rhinitis (AR) and establish objective biomarkers for efficacy monitoring.

Methods

Fifty-nine AR patients underwent 1-year SCIT. Subjective symptoms were assessed via total nasal symptom score (TNSS), combined symptom/medication score (CSMS), and mini rhinoconjunctivitis quality of life questionnaire (MiniRQLQ). Serum total immunoglobulin E (tIgE), Dermatophagoides species-specific IgE (Der p-sIgE), and component-specific IgE (Der p1/2/10/23) were measured. IgE-facilitated allergen binding (IgE-FAB) assay evaluated blocking antibody activity.

Results

The mean TNSS, CSMS, and MiniRQLQ scores were significantly reduced by 28.60% (p < 0.001), 28.60% (p = 0.006), and 24.30% (p < 0.001) respectively after 1 year of SCIT treatment. SCIT treatment significantly elevated serum tIgE and Der p sIgE levels (p < 0.001), with a pronounced increase in component-specific IgE positivity for Der p1 and Der p23 (p < 0.001). The IgE-FAB assay demonstrated that the average suppression of IgE-allergen binding in serum by 1-year SCIT was 4.48% (p < 0.001).

Conclusion

SCIT markedly reduces subjective symptoms in patients with dust mite AR over a 1-year treatment period. Component-sIgE levels and IgE-FAB inhibition could function as objective biomarkers for assessing immunotherapy efficacy, thus facilitating tailored clinical interventions.

目的评价皮下免疫治疗(SCIT)治疗尘螨性变应性鼻炎(AR)的1年疗效,建立客观的疗效监测生物标志物。方法59例AR患者行1年SCIT。主观症状通过鼻症状总评分(TNSS)、症状/药物联合评分(CSMS)和迷你鼻结膜炎生活质量问卷(MiniRQLQ)进行评估。测定血清总免疫球蛋白E (tIgE)、棘球绦虫种特异性IgE (Der p-sIgE)和成分特异性IgE (Der p1/2/10/23)。ige促进过敏原结合(IgE-FAB)试验评估阻断抗体活性。结果TNSS、CSMS、MiniRQLQ平均评分显著降低28.60% (p <;0.001)、28.60% (p = 0.006)和24.30% (p <;0.001)。SCIT治疗显著提高血清tIgE和Der p sIgE水平(p <;0.001), Der p1和Der p23的组分特异性IgE阳性显著增加(p <;0.001)。IgE-FAB检测显示,1年SCIT对血清中ige -过敏原结合的平均抑制率为4.48% (p <;0.001)。结论在1年的治疗期内,SCIT可显著减轻尘螨AR患者的主观症状。组分sige水平和IgE-FAB抑制可以作为评估免疫治疗效果的客观生物标志物,从而促进有针对性的临床干预。
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引用次数: 0
The role of vision therapy in the management of recurrent hordeolum 视力治疗在复发性眼疹治疗中的作用
Pub Date : 2025-04-22 DOI: 10.1002/eer3.70012
Shoubhik Chakraborty, Pallavi Priyadarshini Sahu, Soumya Kanta Mohanty, Hajira R.
<p>Internal hordeolum is characterized by the inflammation of the Meibomian gland due to duct blockage [<span>1</span>]. Recurrent styles are often associated with chronic eye rubbing or lid-fingering habits [<span>2</span>]. The primary causative agent of internal hordeolum is <i>Staphylococcus aureus</i>, with secondary infections arising from an infected chalazion. Clinical signs manifest as localized, firm, red, tender lid swelling or edema. Warm compressions aid in granuloma softening, while antibiotics can be administered locally or systemically [<span>3</span>]. Refractive errors, such as astigmatism, can predispose individuals to hordeolum by inducing eye discomfort, leading to eye poking. Astigmatism often presents with symptoms of asthenopia, and if uncorrected during early childhood, it may result in amblyopia [<span>4</span>].Although optical correction effectively addresses astigmatism, it is insufficient to manage amblyopia. Vision therapy emerges as a pivotal intervention in early childhood or school-age individuals for the effective management of meridional amblyopia [<span>5, 6</span>].</p><p>A 6-year-old female presented to our hospital in August 2023 with a complaint of swelling and pain in her left eyelid. She had previously experienced four episodes of pain and swelling in the previous 3 months, which resolved after using topical antibiotics (Moxifloxacin eye drops 0.5%), NSAIDs, and antibiotic eye ointment (Ocupol). However, the symptoms reappeared. Her right eye's previous prescription was 0.00–1.00 × 180, while her left eye's prescription was −2.00 × 180. However, her parents displayed a lack of adherence to the spectacles' use. Upon examination, her unaided Snellen's visual acuity for distance was 20/40 (6/12) in the right eye and 20/80 (6/24) in the left eye. Following objective refraction and cycloplegic refraction, the final refraction for the right eye was 0.00–1.50 × 180, 20/20 (6/6, N6), and for the left eye, it was 0.00–3.00 × 180, 20/80 (6/24, N18). Anterior segment examination with slit lamp examination unveiled hyperemia and diffuse edema in the upper eyelid and the presence of a swelling that was away from the lid margin and prominent on the palpebral conjunctiva. Posterior segment examination with indirect ophthalmoscope revealed normal findings. Ocular motility was full, free, and painless in all directions. Hirschberg test demonstrated a central corneal reflex. Based on the following findings a diagnosis of acute internal hordeolum with preseptal cellulitis in LE was made. Additionally, a concurrent diagnosis of simple myopic astigmatism with anisometropic amblyopia in the left eye was established.</p><p>In a meticulous non-surgical hordeolum treatment plan, topical antibiotics (Moxifloxacin eye drops 0.5%) with NSAID was given in a dose of 4 times per day which effectively tackles infection and inflammation [<span>7</span>]. Bedtime application of antibiotics eye ointment (Ocupol eye ointment), systemic ant
内痔的特点是由于导管阻塞引起睑板腺的炎症。反复发作的类型通常与长期揉眼睛或用手指抠眼皮的习惯有关。内出血的主要病原体是金黄色葡萄球菌,继发感染由感染的脓肿引起。临床症状表现为局部,硬,红,压痛眼睑肿胀或水肿。热敷有助于肉芽肿软化,而抗生素可局部或全身使用。屈光不正,如散光,会引起眼睛不适,导致眼睛刺痛,从而使人易患眼窝。散光常表现为视疲劳的症状,如果在儿童早期不加以纠正,可能会导致弱视。虽然光学矫正能有效地解决散光问题,但对治疗弱视是不够的。视力治疗成为儿童早期或学龄个体有效治疗子午性弱视的关键干预手段[5,6]。一名6岁女性于2023年8月来我院就诊,主诉左眼睑肿胀疼痛。在过去的3个月里,她曾经历过4次疼痛和肿胀,在使用局部抗生素(0.5%莫西沙星滴眼液)、非甾体抗炎药和抗生素眼膏(Ocupol)后,疼痛和肿胀消退。然而,症状又出现了。右眼既往处方为0.00-1.00 × 180,左眼既往处方为−2.00 × 180。然而,她的父母并没有严格遵守眼镜的使用。经检查,她的裸眼远视灵敏度为右眼20/40(6/12),左眼20/80(6/24)。经物镜屈光和睫状体麻痹屈光后,右眼最终屈光为0.00-1.50 × 180,20 /20 (6/6, N6),左眼最终屈光为0.00-3.00 × 180,20 /80 (6/24, N18)。裂隙灯检查前节段发现上眼睑充血和弥漫性水肿,眼睑边缘肿胀,眼睑结膜突出。间接检眼镜检查后段显示正常。眼动完全、自由、无痛。赫施伯格试验显示角膜中央反射。根据以下发现,诊断为LE的急性内痔合并间隔前蜂窝织炎。此外,单纯性近视散光并发左眼屈光参差性弱视的诊断被确立。在一个细致的非手术治疗方案中,局部抗生素(0.5%莫西沙星滴眼液)和非甾体抗炎药(NSAID)每天给药4次,有效地治疗感染和炎症。睡前应用抗生素眼膏(Ocupol眼膏)、全身抗生素(克拉维酸阿莫西林片375 mg) BD和口服非甾体抗炎药(布洛芬)糖浆进行综合抑菌和止痛,疗程5 d。空腹血糖和餐后血糖分别为80 mg/dL和110 mg/dL。这两项读数都在正常范围内,有效地排除了代谢紊乱作为流行性感冒的诱发因素。值得注意的是,15岁以下儿童自身免疫介导型1型糖尿病的发病率一直在以每年2%-5%的速度上升。值得注意的是,在一周内,肿胀减轻,疼痛停止,促使药物逐渐减少。持续的眼睑卫生,包括在家中进行眼睑擦洗和按摩活动,确保持续的清洁和预防性护理。配戴眼镜的最终接受度为右眼0.00 - 1.50 × 180,20 /20 (6/6, N6),左眼0.00/ - 3.00 × 180,20 /80 (6/24, N18)。1个月后随访,患者出现较轻的左眼外眼窝。两周后,患者配戴眼镜后右眼视力20/20 (6/6,N6),左眼视力20/80 (6/24,N18)。屈光保持不变,弱视治疗继续进行。随后的检查包括角膜测量和轴长生物测量,显示K1- 43.76 × 5°,K2- 45.26 × 95°;右眼轴长23.24 mm,左眼K1- 43.45 × 6°,K2- 47.17 × 96°,轴长22.95 mm。通过沃斯四点测试的感官评价显示左眼抑制,使用随机立体视觉测试的距离和近距离立体视觉小于400秒弧。第一次就诊的视正参数测试显示,患者的所有双目参数均受到影响,随后建议她进行视力治疗,计划每天1小时,持续15天。15天后,右眼BCVA(辅助)为20/20 (6/6,N6),左眼为20/20 (6/6,N6)。 运动频率逐渐减少,随后使用读卡器和抗抑制眼镜(每天1小时)进行连续的家庭二分性训练。在建议逐渐减少的同时,我们遵循Mitchell的指南来改善适应性收敛障碍[9]的双眼视觉参数。1个月后复查,双目视力指标均有明显改善,双目视力恢复。在视力治疗之间和期间也没有复发的证据。上一疗程结束后,我们再次进行了正视光学参数的重新评估,与前一次就诊相比有明显变化(见表1)。患者停药1个月后进行随访,视力无恶化,眼睑无复发性肿胀,见图1。在我们的案例中,孩子没有很好地配合补丁。由于儿童对贴片治疗的依从性不足,我们选择了另一种方法,即实施积极的办公室治疗bbb。这种方法解决了由于遵从性差造成的限制。它确保了一个更有活力和参与性的方法,以提高治疗效果,使治疗过程,并有可能改善总体结果。每月随访6个月,屈光不正无改变,眼角膜无复发。她的左右眼辅助视力为20/20 (6/6),N6,立体视觉保持相同的120弧度。我们遵循Hess RF等人概述的方法来解决屈光参差性弱视,这是最常见的弱视形式。我们在弱视专科诊所的策略包括最初的单眼治疗,后来结合双眼训练来恢复双眼视力。我们采用了各种技术,如跟踪,跟踪训练,眼手协调与可变刺激大小,并使用Sanet视觉集成器(SVI)软件进行对比。此外,还包括单眼固定双眼视野(MFBF)治疗与HTS iNet和跳眼治疗。我们建议每天在家进行1小时的红绿条形阅读活动,使用红绿拼字眼镜,以促进二分呈现。目标是增强视觉集中和改进视觉搜索,特别关注目标分离。我们的指导原则是基于最小的可辨别性,旨在通过追踪和跟踪训练来提高追踪和扫视能力。在单眼固定双眼视场(MFBF)治疗下,我们通过不同对比度和刺激大小刺激“what”和“where”机制,以背侧和腹侧通路为目标。我们的大部分治疗都集中在让大脑处理视觉信息上,如图2所示。一只眼睛的视力模糊会引起不适,导致眼睛摩擦,这是患眼黄疸的一个危险因素。我们的病人有揉眼睛的习惯。双目视力减轻局部不适,从而停止揉眼活动。最近的研究强调了对弱视进行修补治疗的心理上的不情愿。本病例不仅拓宽了我们治疗复发性眼瞳伴屈光参差性弱视的视角,而且强调了我们在非手术方法和各种药物治疗急性眼瞳方面的成功。本病例报告阐述了一种独特的方法来治疗眼附件疾病,如眼盲症,展示了视力治疗在综合眼科护理中的疗效。Shoubhik Chakraborty:概念化(lead);数据管理(领导);形式分析(引线);资源(平等);监督(平等)。Pallavi Priyadarshini Sahu:调查(领导);资源(支持);监督(支持)。Soumya Kanta Mohanty:概念化(平等);调查(平等);方法(平等);资源(平等);监督(平等)。Hajira R.:监督(平等);写作—评审与编辑(同等)。作者声明无利益冲突。卡林加医学科学研究所伦理委员会放弃了对病例报告进行伦理批准的需要。
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引用次数: 0
The third dimension—Eye surgery and stereopsis 第三维度——眼外科和立体视觉
Pub Date : 2025-04-18 DOI: 10.1002/eer3.70011
Divya Trivedi

“Inject visco—the anterior chamber is shallowing!” During my residency, I repeatedly received these orders while performing cataract surgery. My inability to assess the need for more viscoelastic confused me. As a novice surgeon, I attributed these symptoms to my inexperienced hands and embryonic surgical skills. I presumed these would improve with practice, but that didn't seem to happen.

Later, during my LASIK training, my mentor instructed me to lift and reposition the corneal flap. I tried insinuating the instrument under the flap, but it was a struggle. A bandage contact lens eventually had to be placed to cover a corneal epithelial defect caused in the vicinity. I proceeded to the other eye, cautiously this time. I felt I had successfully raised the flap, but my instrument was floating in the air, between the patient's face and the nether end of the microscope!

“You have no depth perception.”—my mentor stated sharply. He ordered an orthoptic evaluation for me. Orthoptics. I vaguely recollected the term from my post-graduate textbooks. “Treatment for accommodation anomalies: Orthoptic exercises”—a segment I had skimmed through for my final examination. Little did I know that I would have to revisit the chapter for my treatment.

The orthoptic evaluation lasted 40 minutes. My convergence facilities were a mere 3 cycles/min, with a remote near point of convergence (22 cm) and a paltry fusional vergence (6∆D). Stereopsis measured 63 s of arc on the random dot stereo-test. That explained my intra-operative challenges. The assessment also revealed an exophoria and an uncorrected compound hypermetropic astigmatism in my left eye. Convergence insufficiency (CI) was the verdict.

I was prescribed 18 days of office-based therapy, which eventually spread across 3 months. This therapy included a diverse range of exercises, a short stint with spectacles, a good deal of patience on my part, and tremendous empathy from the orthoptists, my teachers, and, most of all, my mentor.

Therapy demanded 2 hours of focused exercises every day. An hour in the morning, followed by another grueling hour in the evening. A wide array of exercises was prescribed to correct my proximal and tonic convergence [1]. I was started on various vectographs to increase my positive fusional amplitude. A blurry airplane flying across the Chicago skyline would appear nearer, then farther, as I adjusted the slide holder on the dual polychrome illuminator trainer. To improve my eyes' ability to converge, I worked with a barrel card and brock string, fusing the beads, and trying to maintain their union [2]. The initial days were taxing—the exercises triggered a nagging headache that persisted throughout the day. Nevertheless, I adapted to the unremitting strain of continuously adducting my eyes. My near point of convergence inched closer, reducing the effort I needed for convergence. Stereograms were introduced, in the form of the

“注射黏液——前房变浅了!”在实习期间,我在做白内障手术时反复接到这样的命令。我无法评估是否需要更多的粘弹性,这让我很困惑。作为一名外科新手,我将这些症状归因于我缺乏经验的双手和胚胎手术技巧。我以为这些会随着练习而提高,但这似乎并没有发生。后来,在我的LASIK训练中,我的导师指导我抬起并重新定位角膜瓣。我试着把仪器放到盖子下面,但好不容易。绷带隐形眼镜最终必须被放置以覆盖附近角膜上皮缺损。我又去看另一只眼睛,这次小心翼翼。我觉得我已经成功地抬起了皮瓣,但我的仪器漂浮在空气中,在病人的脸和显微镜的下端之间!“你没有深度知觉。我的导师厉声说。他给我做了一个正视镜检查。视轴矫正法。我模模糊糊地想起了研究生课本上的这个词。“调节异常的治疗:正视练习”——这是我期末考试时略读的一部分。我一点也不知道,为了我的治疗,我不得不重温这一章。正视评估持续40分钟。我的辐合设施只有3圈/分钟,有一个遥远的近辐合点(22厘米)和一个微不足道的融合辐合点(6∆D)。立体视觉在随机点立体测试上测得63 s弧。这就解释了我在手术中的挑战。检查还发现我的左眼有远视和未矫正的复合远视散光。结论是收敛不足(CI)。医生给我开了18天的办公室治疗,最终持续了3个月。这种治疗包括各种各样的练习,戴眼镜的短暂时间,我的耐心,以及骨科医生,老师,最重要的是,我的导师的巨大同情。治疗要求每天进行2小时的集中锻炼。早上一个小时,晚上又熬一个小时。医生给我开了各种各样的练习来矫正我的近端和强音收敛[1]。我开始用各种矢量图来增加我的正融合振幅。一架模糊的飞机飞过芝加哥的天际线,在我调整双彩色照明器训练机上的滑动架时,会显得更近,然后更远。为了提高我眼睛的会聚能力,我使用了一个桶卡和一根细绳,将珠子融合在一起,并试图保持它们的结合。最初的几天很累——锻炼引发了持续一整天的头痛。尽管如此,我还是适应了不断内收眼睛的不懈劳累。我的近收敛点逐渐靠近,减少了收敛所需的努力。以猫卡测试的形式引入了立体图,以提高我的融合幅度。我能看见两只猫并排在一起。中间的第三只猫的出现是短暂的,长着胡须和尾巴。获得这种经常反复无常的猫的持续形象的可视化能力是一项艰巨的任务。然而,经过不懈的努力,第三只猫的形象清晰地出现了。我的适应能力通过哈特图表练习得到了纠正。这些实验涉及刺激位置的重复大振幅变化,在较大的远距离哈特图和较小的手持哈特图之间快速交替。随着时间的推移,我毫不费力地在两张图表之间转移焦点,清晰地看到了每一张图表上的文字。棱镜鳍状物有助于提高速度,减少我的融合收敛的延迟。使用光圈规则训练器,我被要求透过安装在支架上的光圈幻灯片,从下面的卡片中获得清晰、单一的图像。卡片逐渐向孔滑块移动,逐渐增加了我内侧直肌的压力。从感知两个独立的图像到融合它们,最后给它们添加第三个维度,矫正医生帮助我通过了三个等级的双眼视觉。视力治疗的成功与否主要取决于症状的改善情况。3个月后,我在手术显微镜下观察眼组织的方式有了明显的改善(近会聚点6cm;融合辐合14∆D;汇聚设备12次/分;立体视觉(30秒弧度)。角膜瓣很容易进入视野。前房成为一个动态的实体——在白内障手术的不同阶段,前房变深变浅——显然需要粘弹性材料。我的手术技术有了很大的提高。大多数评估视力治疗效果的研究报告说,这些练习的成功率很高。 在20世纪40年代被诊断为CI的1931名患者中,72%的人被认为“治愈”,19%的人“好转”,还有9%的人“失败”。然而,由于每组作者都制定了自己的标准[4],因此没有标准标准来确定哪些患者属于每种类别。因此,我不知道治疗会以我观察和实施手术的方式带来如此惊人的改善。多年来,这种改进一直保持得很好。早在1855年,Von Graefe b[5]就描述了CI。这是一种众所周知的疾病,据报道患病率在2.25%至8.3%之间。眼疲劳、视力模糊和头痛是[7]的临床特征。然而,我从来没有经历过这些症状。在开始手术训练之前,我也没有其他明显的视力问题。我的导师注意到的深度感知的缺乏,是我眼中唯一表明收敛能力不足的迹象。我的经历让我意识到,其他有类似情况的眼科医生在没有正确诊断的情况下也很挣扎。实习期外科医生在开始实习前对其进行正视镜评估的必要性是显而易见的。眼科手术涉及几种透明结构——角膜层、房水、粘弹性、前囊、皮质物质、后囊和玻璃体深度,这是它们的主要区别因素。可视化这些组织需要两只眼睛协调工作,利用我们视觉中的第三维度。因此,双眼视力障碍的早期诊断将极大地帮助年轻外科医生在他们职业生涯的门槛上发展手术能力,给他们的信心带来无价的提升。眼科医生把视力作为宝贵的礼物送给了病人——为什么不愿意把同样的礼物送给我们自己呢?Divya Trivedi:概念化(平等);数据管理(相等);调查(平等);方法(平等);可视化(平等);写作-原稿(同等);写作—评审与编辑(同等)。作者声明无利益冲突。
{"title":"The third dimension—Eye surgery and stereopsis","authors":"Divya Trivedi","doi":"10.1002/eer3.70011","DOIUrl":"https://doi.org/10.1002/eer3.70011","url":null,"abstract":"<p>“Inject visco—the anterior chamber is shallowing!” During my residency, I repeatedly received these orders while performing cataract surgery. My inability to assess the need for more viscoelastic confused me. As a novice surgeon, I attributed these symptoms to my inexperienced hands and embryonic surgical skills. I presumed these would improve with practice, but that didn't seem to happen.</p><p>Later, during my LASIK training, my mentor instructed me to lift and reposition the corneal flap. I tried insinuating the instrument under the flap, but it was a struggle. A bandage contact lens eventually had to be placed to cover a corneal epithelial defect caused in the vicinity. I proceeded to the other eye, cautiously this time. I felt I had successfully raised the flap, but my instrument was floating in the air, between the patient's face and the nether end of the microscope!</p><p>“You have no depth perception.”—my mentor stated sharply. He ordered an orthoptic evaluation for me. Orthoptics. I vaguely recollected the term from my post-graduate textbooks. “Treatment for accommodation anomalies: Orthoptic exercises”—a segment I had skimmed through for my final examination. Little did I know that I would have to revisit the chapter for my treatment.</p><p>The orthoptic evaluation lasted 40 minutes. My convergence facilities were a mere 3 cycles/min, with a remote near point of convergence (22 cm) and a paltry fusional vergence (6∆D). Stereopsis measured 63 s of arc on the random dot stereo-test. That explained my intra-operative challenges. The assessment also revealed an exophoria and an uncorrected compound hypermetropic astigmatism in my left eye. Convergence insufficiency (CI) was the verdict.</p><p>I was prescribed 18 days of office-based therapy, which eventually spread across 3 months. This therapy included a diverse range of exercises, a short stint with spectacles, a good deal of patience on my part, and tremendous empathy from the orthoptists, my teachers, and, most of all, my mentor.</p><p>Therapy demanded 2 hours of focused exercises every day. An hour in the morning, followed by another grueling hour in the evening. A wide array of exercises was prescribed to correct my proximal and tonic convergence [<span>1</span>]. I was started on various vectographs to increase my positive fusional amplitude. A blurry airplane flying across the Chicago skyline would appear nearer, then farther, as I adjusted the slide holder on the dual polychrome illuminator trainer. To improve my eyes' ability to converge, I worked with a barrel card and brock string, fusing the beads, and trying to maintain their union [<span>2</span>]. The initial days were taxing—the exercises triggered a nagging headache that persisted throughout the day. Nevertheless, I adapted to the unremitting strain of continuously adducting my eyes. My near point of convergence inched closer, reducing the effort I needed for convergence. Stereograms were introduced, in the form of the ","PeriodicalId":100519,"journal":{"name":"Eye & ENT Research","volume":"2 2","pages":"145-146"},"PeriodicalIF":0.0,"publicationDate":"2025-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eer3.70011","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144503187","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Global utilization of artificial intelligence in the diagnosis and management of voice disorders over the past five years 在过去五年中,人工智能在语音障碍诊断和管理中的全球应用
Pub Date : 2025-04-03 DOI: 10.1002/eer3.70006
Amna Suleman, Amy L. Rutt

Objective

This review evaluates the worldwide use of artificial intelligence (AI) for the diagnosis and treatment of voice disorders.

Methods

An electronic search was completed in Embase, Pubmed, Ovid MEDLINE, Scopus, Google Scholar, and Web of Science. Studies in English from 2019 to 2024 evaluating the use of AI in detection and management of voice disorders were included. Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines were followed.

Results

Eighty-one studies were recognized. Thirty-three studies were chosen and screened for quality assessment. Of these, 16 studies used AI to determine normal versus pathological voice. The convolutional neural network (CNN) was the most employed algorithm among all machine learning algorithms.

Conclusion

This review revealed significant interest worldwide in utilizing AI in detection of voice disorders. Gaps included the use of limited, inconsistent data sets, lack of validation, and emphasis on detection rather than treatment of the voice disorder. These are areas of opportunity for AI techniques to improved diagnostic accuracy.

目的综述人工智能(AI)在语音障碍诊断和治疗中的应用。方法在Embase、Pubmed、Ovid MEDLINE、Scopus、谷歌Scholar和Web of Science中进行电子检索。纳入了2019年至2024年的英语研究,评估了人工智能在语音障碍检测和管理中的应用。遵循系统评价和荟萃分析指南的首选报告项目。结果共确认81项研究。选择33项研究进行质量评估。其中,有16项研究使用人工智能来确定正常和病理的声音。卷积神经网络(CNN)是所有机器学习算法中使用最多的算法。结论本综述揭示了世界范围内利用人工智能检测语音障碍的重大兴趣。差距包括使用有限,不一致的数据集,缺乏验证,强调检测而不是治疗语音障碍。这些都是人工智能技术提高诊断准确性的机会。
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引用次数: 0
Realistic 3D-printed sinus anatomical model and rigid nasal endoscopy: Unique approach to teach medical students intranasal anatomy 逼真的3d打印鼻窦解剖模型和刚性鼻内窥镜:教授医学生鼻内解剖的独特方法
Pub Date : 2025-04-03 DOI: 10.1002/eer3.70010
Heather L. Johns, Pablo C. Ochoa, Jamie O’Byrne, Christian Hanson, Victoria Sears, Jonathan Morris, Semirra Bayan, Janalee Stokken

Purpose

The small and complex space of the intranasal cavity poses a challenge to teaching and learning sinonasal anatomy in undergraduate medical education. Evidence suggests that utilizing 3D-printed (3DP) models is an effective means to comprehend anatomical structures and their spatial relationships. In this study, we introduce and evaluate the educational value of rigid nasal endoscopy on realistic 3DP and silicone-cast sinus models as a method to teach medical students intranasal anatomy.

Methods

Twelve first-year medical students participated in an educational rigid-nasal endoscopy workshop led by Otolaryngology PGY-2 residents and rhinology consultants. The workshop consisted of (1) an introductory PowerPoint on rigid nasal endoscopy and basic intranasal anatomy, (2) timed trials that tested students' ability to locate intranasal anatomical structures while scoping with a rigid endoscope, and (3) pre- and post-surveys.

Results

Participants improved in their ability to locate each intranasal anatomical structure during the timed trials. Participants felt that rigid endoscopy of 3DP models was an effective method to learn intranasal anatomy compared to their traditional medical school anatomy course.

Conclusion

The results of this study suggest that rigid nasal endoscopy of 3DP sinus models is a potentially high-value educational method for teaching intranasal anatomy to first-year medical students. Students enjoyed the opportunity to learn intranasal anatomy while practicing a clinically relevant procedure - rigid nasal endoscopy.

目的鼻内腔空间小而复杂,对医学本科教学中鼻解剖的教学提出了挑战。有证据表明,利用3d打印(3DP)模型是理解解剖结构及其空间关系的有效手段。在本研究中,我们介绍和评估刚性鼻内窥镜在真实3d打印和硅胶铸造鼻窦模型上的教学价值,作为一种教授医学生鼻内解剖学的方法。方法12名一年级医学生参加由耳鼻喉科PGY-2住院医师和鼻内科顾问主持的刚性鼻内窥镜教育性研讨会。研讨会包括(1)关于刚性鼻内窥镜和基本鼻内解剖学的介绍性ppt,(2)测试学生在使用刚性鼻内窥镜检查时定位鼻内解剖结构的能力的定时试验,以及(3)前后调查。结果在计时试验中,受试者对鼻内解剖结构的定位能力有所提高。参与者认为,与传统的医学院解剖学课程相比,3d打印模型的刚性内窥镜检查是学习鼻内解剖学的有效方法。结论本研究结果提示,在医学一年级学生的鼻内解剖学教学中,刚性鼻内窥镜3d打印鼻窦模型是一种潜在的高价值的教学方法。学生们在学习鼻内解剖学的同时,还练习了一项临床相关的手术——刚性鼻内窥镜检查。
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引用次数: 0
Characterization of eosinophil populations in a murine model of type 2 airway inflammation via flow cytometry 通过流式细胞术表征小鼠2型气道炎症模型中的嗜酸性粒细胞群体
Pub Date : 2025-03-30 DOI: 10.1002/eer3.70009
Huiqing Wang, Qidi Zhang, Yang Wang, Rongqing Zhang, Bing Yan

Purpose

This study aims to optimize experimental conditions to obtain a larger quantity of eosinophils from the type 2 inflammation mouse model, which will serve as a basis for further investigation into the role and mechanisms of eosinophils in type 2 inflammation.

Methods

We used a mouse model of type 2 inflammation and isolated potential eosinophil-resident tissues (bone marrow, spleen, and nasal mucosa) for flow cytometry analysis. By combining forward scatter, side scatter, and the cell population identified as CD45+ (protein tyrosine phosphatase receptor type C) CD11b+ (integrin alpha-M) Ly6G (lymphocyte antigen 6 family member G) Siglec-F+ (sialic acid-binding immunoglobulin-like lectin F), we characterized eosinophils.

Results

The results showed that the number and proportion of eosinophils in bone marrow were numerically higher compared to the spleen and nasal mucosa. Further exploration of conditions may provide guarantees for the later development of mechanism research.

Conclusion

These findings provide clues for further optimizing experimental conditions to obtain sufficient eosinophils from bone marrow for mechanistic studies. They also offer a potential framework for exploring phenotypic heterogeneity and functional studies of eosinophils in various tissues.

本研究旨在优化实验条件,从2型炎症小鼠模型中获得更大量的嗜酸性粒细胞,为进一步研究嗜酸性粒细胞在2型炎症中的作用和机制奠定基础。方法采用小鼠2型炎症模型和分离的潜在嗜酸性粒细胞驻留组织(骨髓、脾脏和鼻黏膜)进行流式细胞术分析。通过结合前向散射、侧向散射和鉴定为CD45+(蛋白酪氨酸磷酸酶受体C型)CD11b+(整合素α - m) Ly6G−(淋巴细胞抗原6家族成员G) siglece -F+(唾液酸结合免疫球蛋白样凝集素F)的细胞群,我们鉴定了嗜酸性粒细胞。结果小鼠骨髓中嗜酸性粒细胞的数量和比例明显高于脾脏和鼻黏膜。对条件的进一步探索可为今后机理研究的开展提供保障。结论本研究结果为进一步优化从骨髓中获得充足嗜酸性粒细胞的实验条件提供了线索。它们也为探索各种组织中嗜酸性粒细胞的表型异质性和功能研究提供了一个潜在的框架。
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引用次数: 0
Variant distribution and characterization of hereditary hemorrhagic telangiectasia in Chinese patients 中国遗传性出血性毛细血管扩张的变异分布和特征
Pub Date : 2025-03-29 DOI: 10.1002/eer3.70005
Yali Zhao, Xiangdong Wang, Yuhui Ouyang, Lin Xi, Yuan Zhang, Yan Zhao

Background

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disorder with variable manifestations, including recurrent epistaxis, telangiectasias, arteriovenous malformations, and family history. It is caused by heterozygous null alleles of ENG, ACVRL1, SMAD4, or BMP9, with delayed clinical diagnosis. Genetic testing is crucial for early diagnosis.

Objective

To analyze the variant distribution of HHT-related genes, expand variant databases for Chinese patients, and explore phenotype-genotype associations.

Methods

Thirty-two individuals from 20 unrelated families were recruited. Coding regions of ENG, ACVRL1, SMAD4, and BMP9 were sequenced. Variants were identified by sequence alignment. Epistaxis severity was evaluated using the epistaxis severity score (ESS), and the ESS differences between groups were analyzed using the Mann–Whitney test.

Results

Seventeen unique variants were identified in 17 unrelated HHT families (17/20, 85%), including 5 novel variants (3 in ENG and 2 in ACVRL1). Eleven ACVRL1 variants were identified in 12 families (12/17, 70.6%). Six variants of ENG were detected in 5 families (5/17, 29.4%), and one patient had two variants. ACVRL1 variants were 2.4 times more prevalent than ENG variants, with 41.7% of ACVRL1 variants in exon 10. A recurrent variant, c.1435C>T, was identified in two families. Epistaxis severity increased with age.

Conclusions

ACVRL1 variants were more common than ENG variants in Chinese HHT families, with exon 10 identified as a potential hotspot. These findings enhance understanding of HHT genetics and guide targeted genetic testing in China.

背景:遗传性出血性毛细血管扩张症(HHT)是一种常染色体显性遗传病,表现多样,包括复发性鼻出血、毛细血管扩张、动静脉畸形和家族史。它是由ENG、ACVRL1、SMAD4或BMP9的杂合零等位基因引起的,临床诊断延迟。基因检测对早期诊断至关重要。目的分析hht相关基因的变异分布,扩大中国患者的变异数据库,探讨表型与基因型的相关性。方法从20个非亲属家庭中招募32名个体。对ENG、ACVRL1、SMAD4和BMP9的编码区进行测序。通过序列比对鉴定变异。采用鼻出血严重程度评分(ESS)评估鼻出血严重程度,采用Mann-Whitney检验分析各组间ESS差异。结果17个HHT家族(17/20,85%)鉴定出17个独特变异,其中5个新变异(3个在ENG中,2个在ACVRL1中)。在12个家族中鉴定出11个ACVRL1变异(12/17,70.6%)。5个家族(5/17,29.4%)检测到6个变异,1例患者有2个变异。ACVRL1变异是ENG变异的2.4倍,41.7%的ACVRL1变异位于第10外显子。在两个家族中发现了c.1435C>;T的复发变体。鼻出血严重程度随年龄增长而增加。结论ACVRL1变异在中国HHT家族中比ENG变异更常见,外显子10被认为是潜在的热点。这些发现增强了对HHT遗传学的认识,并指导了中国有针对性的基因检测。
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引用次数: 0
期刊
Eye & ENT Research
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