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.
{"title":"Epidemiology of common allergic diseases in China: Current position and implications","authors":"Xu Xu, Chengshuo Wang, Luo Zhang, Jingyun Li, Yuan Zhang","doi":"10.1002/eer3.70016","DOIUrl":"https://doi.org/10.1002/eer3.70016","url":null,"abstract":"<p>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.</p>","PeriodicalId":100519,"journal":{"name":"Eye & ENT Research","volume":"2 2","pages":"77-87"},"PeriodicalIF":0.0,"publicationDate":"2025-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eer3.70016","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144502952","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}
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。
{"title":"Glioblastoma multiforme with transdural extension to the external auditory canal via the tegmen tympani—Clinical report with review of the literature","authors":"Arba Cecia, Emal Lesha, David G. Laird, Elsa Nico, Kaan Yagmurlu, Bruce L. Fetterman, L. Madison Michael II","doi":"10.1002/eer3.70015","DOIUrl":"https://doi.org/10.1002/eer3.70015","url":null,"abstract":"<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","PeriodicalId":100519,"journal":{"name":"Eye & ENT Research","volume":"2 2","pages":"141-144"},"PeriodicalIF":0.0,"publicationDate":"2025-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eer3.70015","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144502982","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}
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.
{"title":"Activation and inhibition of Notch signaling facilitate proliferative regeneration of sensory cells in adult mice","authors":"Shan Zeng, Tao Jiang, Zhengyi Chen, Huawei Li, Luo Guo, Wenyan Li","doi":"10.1002/eer3.70008","DOIUrl":"https://doi.org/10.1002/eer3.70008","url":null,"abstract":"<p>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.</p>","PeriodicalId":100519,"journal":{"name":"Eye & ENT Research","volume":"2 2","pages":"104-115"},"PeriodicalIF":0.0,"publicationDate":"2025-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eer3.70008","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144502984","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}