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本文引用的文献

1
Fine-needle aspiration in the diagnosis of head and neck lesions: a review and discussion of problems in differential diagnosis.细针穿刺在头颈部病变诊断中的应用:鉴别诊断问题的综述与讨论
Diagn Cytopathol. 2007 Dec;35(12):798-805. doi: 10.1002/dc.20769.
2
Promising clinical efficacy of streptomycin-rifampin combination for treatment of buruli ulcer (Mycobacterium ulcerans disease).链霉素-利福平联合用药治疗布鲁里溃疡(溃疡分枝杆菌病)具有良好的临床疗效。
Antimicrob Agents Chemother. 2007 Nov;51(11):4029-35. doi: 10.1128/AAC.00175-07. Epub 2007 May 25.
3
"Rapid-impact interventions": how a policy of integrated control for Africa's neglected tropical diseases could benefit the poor.“快速影响干预措施”:非洲被忽视热带病综合防治政策如何惠及贫困人口。
PLoS Med. 2005 Nov;2(11):e336. doi: 10.1371/journal.pmed.0020336. Epub 2005 Oct 11.
4
Sensitivity of PCR targeting the IS2404 insertion sequence of Mycobacterium ulcerans in an Assay using punch biopsy specimens for diagnosis of Buruli ulcer.使用打孔活检标本诊断布鲁里溃疡的检测中,针对溃疡分枝杆菌IS2404插入序列的PCR敏感性
J Clin Microbiol. 2005 Aug;43(8):3650-6. doi: 10.1128/JCM.43.8.3650-3656.2005.
5
Buruli ulcer recurrence, Benin.贝宁,布鲁里溃疡复发。
Emerg Infect Dis. 2005 Apr;11(4):584-9. doi: 10.3201/eid1104.041000.
6
A simple PCR method for rapid genotype analysis of Mycobacterium ulcerans.一种用于快速分析溃疡分枝杆菌基因型的简单聚合酶链反应方法。
J Clin Microbiol. 2000 Apr;38(4):1482-7. doi: 10.1128/JCM.38.4.1482-1487.2000.
7
Fine needle aspiration (FNA) cytology in tuberculous lymphadenitis.结核性淋巴结炎的细针穿刺抽吸(FNA)细胞学检查
Cytopathology. 1998 Jun;9(3):201-7. doi: 10.1046/j.1365-2303.1998.00073.x.
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Effectiveness of excision of pre-ulcerative Buruli lesions in field situations in a rural district in Ghana.
Trop Doct. 1998 Apr;28(2):81-3. doi: 10.1177/004947559802800208.
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Direct detection and identification of Mycobacterium ulcerans in clinical specimens by PCR and oligonucleotide-specific capture plate hybridization.通过聚合酶链反应(PCR)和寡核苷酸特异性捕获平板杂交技术直接检测和鉴定临床标本中的溃疡分枝杆菌。
J Clin Microbiol. 1997 May;35(5):1097-100. doi: 10.1128/jcm.35.5.1097-1100.1997.
10
Variability in 3' end of 16S rRNA sequence of Mycobacterium ulcerans is related to geographic origin of isolates.溃疡分枝杆菌16S rRNA序列3'端的变异性与分离株的地理来源有关。
J Clin Microbiol. 1996 Apr;34(4):962-5. doi: 10.1128/jcm.34.4.962-965.1996.

利用细针穿刺抽吸物进行针对溃疡分枝杆菌的聚合酶链反应检测以诊断布氏溃疡的敏感性

Sensitivity of PCR targeting Mycobacterium ulcerans by use of fine-needle aspirates for diagnosis of Buruli ulcer.

作者信息

Phillips R O, Sarfo F S, Osei-Sarpong F, Boateng A, Tetteh I, Lartey A, Adentwe E, Opare W, Asiedu K B, Wansbrough-Jones M

机构信息

Kwame Nkrumah University of Science and Technology, Kumasi, Ghana.

出版信息

J Clin Microbiol. 2009 Apr;47(4):924-6. doi: 10.1128/JCM.01842-08. Epub 2009 Feb 9.

DOI:10.1128/JCM.01842-08
PMID:19204098
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2668351/
Abstract

In a previous study, we reported that the sensitivity of PCR targeting the IS2404 insertion sequence of Mycobacterium ulcerans was 98% when it was applied to 4-mm punch biopsy samples of Buruli lesions. Fine-needle aspiration (FNA) is a less traumatic sampling technique for nonulcerated lesions, and we have studied the sensitivity of PCR using FNA samples. Fine-needle aspirates were taken with a 21-gauge needle from 43 patients diagnosed clinically with M. ulcerans disease. Four-millimeter punch biopsies were obtained for microscopy, culture, and PCR targeting the IS2404 insertion sequence. The sensitivity of PCR using samples obtained by FNA was 86% (95% confidence interval [95% CI], 72 to 94%) compared with that for PCR using punch biopsy samples. In this study, the sensitivities of culture and microscopy for punch biopsy samples were 44% (95% CI, 29 to 60%) and 26% (95% CI, 14 to 41%), respectively. This demonstrates that PCR on an FNA sample is a viable minimally invasive technique to diagnose M. ulcerans lesions.

摘要

在之前的一项研究中,我们报告称,将针对溃疡分枝杆菌IS2404插入序列的聚合酶链反应(PCR)应用于布氏溃疡病变的4毫米钻孔活检样本时,其敏感性为98%。细针穿刺抽吸术(FNA)对于未溃疡病变来说是一种创伤较小的采样技术,并且我们已经研究了使用FNA样本进行PCR的敏感性。用21号针从43例临床诊断为溃疡分枝杆菌病的患者身上获取细针抽吸物。获取4毫米的钻孔活检样本用于显微镜检查、培养以及针对IS2404插入序列的PCR。与使用钻孔活检样本进行PCR相比,使用FNA获取的样本进行PCR的敏感性为86%(95%置信区间[95%CI],72%至94%)。在本研究中,钻孔活检样本的培养和显微镜检查敏感性分别为44%(95%CI,29%至60%)和26%(95%CI,14%至41%)。这表明对FNA样本进行PCR是诊断溃疡分枝杆菌病变的一种可行的微创技术。