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简化的细胞培养方法用于诊断非典型性原发性纤毛运动障碍。

Simplified cell culture method for the diagnosis of atypical primary ciliary dyskinesia.

机构信息

Department of Pediatrics, University of Pisa, Via Roma 67, 56126 Pisa, Italy.

出版信息

Thorax. 2009 Dec;64(12):1077-81. doi: 10.1136/thx.2008.110940. Epub 2009 Sep 21.

Abstract

BACKGROUND

The diagnosis of primary ciliary dyskinesia (PCD) can be challenging, and it may be particularly difficult to distinguish primary ciliary disease from the secondary changes after infections.

OBJECTIVES

The purpose of the study was to evaluate if nasal epithelial cells, obtained with nasal brushing instead of a biopsy, could be used in a culture system for the diagnosis of PCD in difficult cases.

METHODS AND MAIN RESULTS

Ciliary motion analysis (CMA) and transmission electron microscopy (TEM) were performed on 59 subjects with persistent or recurrent pneumonia. These investigations allowed the diagnosis of PCD in 13 (22%) patients while the defect of the cilia was considered secondary to infections in 37 (63%) subjects. In the remaining nine (15%) patients the diagnostic evaluation with CMA and TEM remained inconclusive. Ciliogenesis in culture allowed the diagnosis of PCD in four of these patients, it was indicative of a secondary defect in two subjects, and it was not helpful in the remaining three patients.

CONCLUSIONS

Culture of cells obtained with brushing of the nasal turbinate is not a perfect test, nevertheless it may offer diagnostic help in doubtful cases of PCD.

摘要

背景

原发性纤毛运动障碍(PCD)的诊断具有挑战性,特别是在区分原发性纤毛疾病和感染后的继发性改变时可能较为困难。

目的

本研究旨在评估是否可以使用鼻刷而非活检获得的鼻上皮细胞,用于在疑难病例中建立用于诊断 PCD 的培养系统。

方法和主要结果

对 59 例持续性或复发性肺炎患者进行了纤毛运动分析(CMA)和透射电子显微镜(TEM)检查。这些检查在 13 例(22%)患者中诊断为 PCD,而 37 例(63%)患者的纤毛缺陷被认为继发于感染。在其余 9 例(15%)患者中,CMA 和 TEM 的诊断评估仍不确定。培养中的纤毛发生可在其中 4 例患者中诊断为 PCD,在 2 例患者中提示继发性缺陷,在其余 3 例患者中则无帮助。

结论

用鼻刷获取细胞进行培养并非一项完美的检查,但在可疑的 PCD 病例中,它可能提供诊断帮助。

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