lacrimal

泪道阻塞性疾病
  • 文章类型: Journal Article
    评估内镜辅助的改良Weber-Ferguson方法治疗原发性泪囊肿瘤并延伸到邻近组织的结果。
    对2010年1月至2022年6月在上海市第九人民医院接受内镜辅助改良韦伯-弗格森入路治疗的所有泪囊肿瘤患者进行了回顾性介入研究,中国。评估的数据包括人口统计,临床表现,成像特征,外科技术,组织病理学,辅助管理方式,并发症,和结果。
    共13例患者纳入分析。在84.6%(11/13)的患者中,主诉是主诉。近一半的患者(46.1%,6/13)误诊为泪道阻塞。本系列中的所有泪囊肿瘤在T1加权MRI成像上均显示不均匀的增强。术后,84.6%(11/13)的患者恢复良好,美观良好,平均随访58.6个月,无病。两名接受额外切除的患者在姑息性放化疗期间复发并死亡(随访41和96个月)。
    内窥镜辅助的改良Weber-Fergusson手术入路可有效地提供泪囊肿瘤的更好的可见性和可及性,并延伸到邻近组织。
    To evaluate the outcomes of endoscopy-assisted modified Weber-Ferguson\'s approach in the management of primary lacrimal sac tumors with extension into the neighboring tissues.
    A retrospective interventional study was performed on all patients with lacrimal sac tumors treated with the endoscopy-assisted modified Weber-Ferguson approach between January 2010 and June 2022 at the Shanghai Ninth People\'s Hospital, China. Data assessed include demographics, clinical presentations, imaging features, surgical techniques, histopathology, adjuvant modalities of management, complications, and outcomes.
    A total of 13 patients were included in the analysis. Epiphora and palpable mass lesion were the presenting complaint in 84.6% (11/13) of the patients. Nearly half of the patients (46.1%, 6/13) were misdiagnosed as lacrimal duct obstruction. All the lacrimal sac tumors in the present series showed uneven enhancement on T1-weighted MRI imaging. Postoperatively, 84.6% (11/13) patients recovered well with excellent esthetics and were disease-free after a mean follow-up of 58.6 months. Two patients who underwent additional exenteration developed recurrence and succumbed (at 41 and 96 months follow up) while they were on palliative chemoradiation.
    The endoscopic-assisted modified Weber-Fergusson surgical approach is effective in providing better visibility and accessibility to lacrimal sac tumors with extension into neighboring tissue.
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  • 文章类型: Journal Article
    目的:在临床怀疑患有部分或完全获得性鼻泪管阻塞(PANDO)的患者中,与泪镜检查相比,CT-DCG在确定泪管阻塞的程度和类型方面的功效和局限性。
    方法:对上海市第九人民医院957例原发性获得性鼻泪管阻塞(PANDO)患者的1232例泪道引流系统进行回顾性分析。患者接受CT-DCG检查,并与神经内镜检查和临床检查结果相关。
    结果:在研究的患者中,男性173人,女性784人,年龄在18-93岁之间。在1232条泪道中,980例可获得良好的CT-DCG图像,957例可获得泪镜检查图像。在这些完全阻塞中,有81%(794/980),使用CT-DCG确定了19%(186/980)的部分阻塞。CT-DCG和神经内镜检查显示,梗阻类型的一致性为68.4%,梗阻水平为63%。大多数阻塞发生在囊管交界处(62.5%),其次是鼻泪管的上半部分(27.5%)。梗阻类型与年龄组和症状持续时间的相关性存在显着差异。随着症状持续时间的增加,CT-DCG图像显示的完全泪道阻塞的比例增加,不完全阻塞的比例减少(p=0.015)。
    结论:泪囊与鼻泪管交界处是最常见的阻塞部位。年龄和症状持续时间影响所指出的梗阻类型。调查之间的协议程度和水平是中等的。CT-DCG和神经内镜的组合可以更准确地识别位置。
    OBJECTIVE: To correlate and evaluate the power and limitations of CT-DCG in determining the level and type of lacrimal duct obstruction in comparison to dacryoendoscopy in patients clinically suspected to be having partial or complete primary acquired nasolacrimal duct obstruction (PANDO).
    METHODS: A retrospective chart review was performed on 1232 lacrimal drainage systems of 957 patients who suffered from primary acquired nasolacrimal duct obstruction (PANDO) at Shanghai Ninth People\'s Hospital. Patients were examined with CT-DCG and correlated with dacryoendoscopy and the findings of clinical examination.
    RESULTS: Of the studied patients, 173 were men and 784 were women with an age range of 18-93 years. Of the 1232 lacrimal pathways, good CT-DCG images could be obtained in 980 cases and dacryoendoscopy in 957 cases. Of these complete obstructions were noted in 81% (794/980), and partial obstructions were identified in 19% (186/980) with CT-DCG. CT-DCG and dacryoendoscopy showed 68.4% agreement for the type of the obstruction and 63% for the level of the obstruction. The majority of the obstructions occurred at the sac-duct junction (62.5%) followed by the upper half of the nasolacrimal duct (27.5%). There was a significant difference in the correlation of the obstruction type with age group and with the duration of symptoms. As the duration of symptoms increased, the proportion of complete lacrimal duct obstructions as shown on CT-DCG images increased and the proportion of incomplete obstruction decreased (p = 0.015).
    CONCLUSIONS: The junction of lacrimal sac and nasolacrimal duct was the most common obstruction site. Age and the duration of symptoms influenced the type of obstruction noted. The degree and level of agreement between the investigations was moderate. A combination of CT-DCG and Dacryoendoscopy could together identify the location more accurately.
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  • 文章类型: Letter
    暂无摘要。
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  • 文章类型: Journal Article
    青光眼是一种需要终身治疗的慢性疾病,然而,频繁用药引起的不适可能影响生活质量。此外,由于快速的眼部清除机制和眼部屏障,传统局部给药的治疗效果并不令人满意.在这里,制备了一种聚合物含量低的三交联胶束-水凝胶泪道植入物,用于青光眼的局部和长期治疗。拉坦前列素和噻吗洛尔同时以高包封率包埋在PEG-PLA胶束中,并进一步加载到三重交联水凝胶中,促进药物的双重持续释放。随后,植入物由独特的分子定向固定技术构建,这使得植入物能够固定在泪管中。三重交联的胶束-水凝胶泪管植入物表现出显著的物理化学特征,以维持拉坦前列素和噻吗洛尔的释放。体外释放实验证明两种药物的持续时间延长长达28天。在兔模型中对升高的眼内压(IOP)的体内测试显示,IOP降低效果如预期的那样持续超过28天。泪道植入物的相对药理学可用性(PA)是滴眼剂的5.7倍。对眼部刺激和组织学检查的研究结果表明,泪道植入物具有良好的安全性。总之,三重交联胶束-水凝胶泪道植入物可以有效降低IOP,具有出色的相容性,证明了青光眼长期无创治疗的前景。
    Glaucoma is a chronic disease that requires lifelong treatment, whereas, discomfort caused by frequent medication may affect the quality of life. Moreover, the therapeutic efficacy of traditional local administration was unsatisfactory due to the rapid ocular clearance mechanism and the ocular barrier. Herein, a triple crosslinked micelle-hydrogel lacrimal implant with low polymer content was fabricated for localized and prolonged therapy of glaucoma. Latanoprost and timolol were simultaneously entrapped in the PEG-PLA micelles with high encapsulation efficiency and further loaded into the triple crosslinked hydrogel, facilitating a double sustained release of drugs. Subsequently, the implant was constructed by a unique molecular orientation fixation technology, which enables the implant to be fixed in the lacrimal duct. The triple crosslinked micelle-hydrogel lacrimal implant manifested a distinguished physicochemical characterization to sustain the release of latanoprost and timolol. In vitro release experiment demonstrated the duration of two drugs was extended for up to 28 days. The in vivo test of elevated intraocular pressure (IOP) in a rabbit model revealed that the IOP-lowering effects were sustained longer than 28 days as expected. The relative pharmacological availability (PA) of lacrimal implants was 5.7 times greater than that of the eye drops. The results of the studies on ocular irritation and histological examination demonstrated the good safety of the lacrimal implant. In conclusion, the triple crosslinked micelle-hydrogel lacrimal implant could effectively lower the IOP with splendid compatibility, demonstrating the promising prospect in the long-term noninvasive treatment of glaucoma.
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