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原发性纤毛运动障碍病例的支气管镜检查取样及透射电子显微镜分析:原发性纤毛运动障碍的取样与诊断

Primary ciliary dyskinesia cases bronchoscopic sampling and TEM analysis: sampling & diagnosis in PCD.

作者信息

Doğan Mülazimoğlu Deniz, Evirgen Oya, Kayacan Oya, Karnak Demet

机构信息

Department of Chest Diseases, Ankara University School of Medicine, Ankara, Turkiye.

Department of Histology and Embryology, Ankara University School of Medicine, Ankara, Turkiye.

出版信息

Ultrastruct Pathol. 2025;49(4):371-376. doi: 10.1080/01913123.2025.2498418. Epub 2025 Apr 30.

Abstract

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.

摘要

原发性纤毛运动障碍(PCD)是一种罕见的、具有遗传异质性的疾病,其特征为纤毛结构和功能受损,导致慢性呼吸道症状和反复感染。尽管其具有临床意义,但由于PCD表现多样且缺乏金标准诊断测试,其诊断仍然具有挑战性。包括新生儿呼吸窘迫和内脏反位缺陷在内的特定临床标准有助于怀疑PCD,但确诊通常需要多种测试相结合。在本研究中,我们旨在评估支气管镜技术在获取用于透射电子显微镜(TEM)分析的呼吸道上皮样本方面的有效性。我们纳入了患有支气管扩张且疑似PCD并接受纤维支气管镜检查的成年人。在清醒镇静下从特定支气管节段获取支气管钳取组织和刷检组织。对组织样本进行处理以进行TEM分析,以识别与PCD相关的超微结构轴丝缺陷。我们的研究包括10名年龄在19 - 38岁之间的患者(3名女性,7名男性),并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,与钳取活检组织样本相比,从刷检组织和钳取活检固定液中获得的沉淀物中,纤毛细胞的存在和纤毛横断面的组织学评分更高。超薄切片的电子显微镜检查显示沉淀物中有丰富的纤毛细胞和异常的纤毛结构,有助于PCD的诊断。PCD是支气管扩张的一个重要病因,强调了准确诊断和适当管理策略的必要性。我们的研究结果强调了支气管镜技术的重要性,包括支气管刷检和钳取活检,以提高诊断率并指导及时干预以改善患者预后。

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