原发性纤毛运动障碍病例的支气管镜取样与透射电镜分析:PCD的取样与诊断。

IF 1.1 4区 医学 Q4 MICROSCOPY
Deniz Doğan Mülazimoğlu, Oya Evirgen, Oya Kayacan, Demet Karnak
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引用次数: 0

摘要

原发性纤毛运动障碍(PCD)是一种罕见的遗传异质性疾病,其特征是纤毛结构和功能受损,导致慢性呼吸道症状和反复感染。尽管PCD具有临床意义,但由于其表现多变且缺乏金标准诊断测试,诊断仍然具有挑战性。具体的临床标准,包括新生儿呼吸窘迫和侧边缺陷,有助于怀疑PCD,但确诊通常需要综合检查。在这项研究中,我们旨在评估支气管镜技术在获取呼吸道上皮样本用于透射电子显微镜(TEM)分析方面的有效性。我们招募了支气管扩张和疑似PCD的成年人,他们接受了纤维支气管镜检查。在清醒镇静下,从特定支气管段取支气管钳和刷活检。组织样本进行TEM分析,以确定与PCD相关的轴突超微结构缺陷。我们的研究纳入了10例患者(3名女性,7名男性),年龄19-38岁,提供了详细的人口统计学和临床特征。对气管支气管活检样本的评估显示,与镊子活检组织样本相比,从刷子活检和固定溶液中获得的颗粒中存在纤毛细胞和纤毛横切面的组织学评分更高。电镜超薄切片显示纤毛细胞丰富,纤毛结构异常,有助于小球PCD的诊断。PCD是支气管扩张的重要病因,强调需要准确的诊断和适当的管理策略。我们的研究结果强调了支气管镜技术的重要性,包括支气管刷牙和镊子活检,在提高诊断率和指导及时干预以改善患者预后方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary ciliary dyskinesia cases bronchoscopic sampling and TEM analysis: sampling & diagnosis in PCD.

Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous disorder characterized by impaired ciliary structure and function, leading to chronic respiratory symptoms and recurrent infections. Despite its clinical significance, PCD diagnosis remains challenging due to its variable presentation and the lack of a gold standard diagnostic test. Specific clinical criteria, including neonatal respiratory distress and laterality defects, aid in suspicion of PCD, but confirmatory diagnosis often requires a combination of tests. In this study, we aimed to assess the efficacy of bronchoscopic techniques in obtaining respiratory epithelial samples for transmission electron microscopy (TEM) analysis. We enrolled adults with bronchiectasis and suspected PCD who underwent fiberoptic bronchoscopy. Bronchial forceps and brush biopsies were obtained from specific bronchial segments under conscious sedation. Tissue samples were processed for TEM analysis to identify ultrastructural axonemal defects associated with PCD. Our study included 10 patients (3 females, 7 males) aged 19-38 years, with detailed demographics and clinical characteristics provided. Evaluation of tracheobronchial biopsy samples revealed higher histological scores for the presence of ciliated cells and transverse sections of cilia in pellets obtained from brush biopsies and fixative solutions of forceps biopsy compared to forceps biopsy tissue samples. Electron microscopic examination of ultra-thin sections demonstrated abundant ciliated cells and abnormal cilia structures, aiding in the diagnosis of PCD in pellets. PCD represents a significant etiology of bronchiectasis, emphasizing the need for accurate diagnosis and appropriate management strategies. Our findings highlight the importance of bronchoscopic techniques, including bronchial brushing alongside forceps biopsies, in enhancing diagnostic yield and guiding timely intervention to improve patient outcomes.

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来源期刊
Ultrastructural Pathology
Ultrastructural Pathology 医学-病理学
CiteScore
2.00
自引率
10.00%
发文量
40
审稿时长
6-12 weeks
期刊介绍: Ultrastructural Pathology is the official journal of the Society for Ultrastructural Pathology. Published bimonthly, we are the only journal to be devoted entirely to diagnostic ultrastructural pathology. Ultrastructural Pathology is the ideal journal to publish high-quality research on the following topics: Advances in the uses of electron microscopic and immunohistochemical techniques Correlations of ultrastructural data with light microscopy, histochemistry, immunohistochemistry, biochemistry, cell and tissue culturing, and electron probe analysis Important new, investigative, clinical, and diagnostic EM methods.
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