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1986 - 1995年影响新西兰儿童的非结核分枝杆菌淋巴结炎的流行病学

The epidemiology of nontuberculous mycobacterial lymphadenitis affecting New Zealand children 1986-95.

作者信息

Howell N, Heaton P A, Neutze J

机构信息

Taranaki Base Hospital, New Plymouth.

出版信息

N Z Med J. 1997 May 9;110(1043):171-3.

PMID:9196503
Abstract

AIMS

To study the epidemiological trends of nontuberculous mycobacterial lymphadenitis affecting New Zealand children from 1986-95.

METHODS

Cases were identified from the records of the three regional reference laboratories in New Zealand. All children of less than 16 years with a positive culture of nontuberculous mycobacteria from a lymph node tissue sample were included.

RESULTS

One hundred and sixty eight cases were identified, 43 in the first 5 years (no data available from Waikato) and 125 in the second 5 years of the study period. One hundred and fifty three (91%) of cases were in the 0-5 year age group and 101 (60%) were female. The head and neck was the most common site of infection accounting for 141 (84%) of all infection. In 161 (96%) of cases the causative organism was Mycobacterium avium intracellulare complex.

CONCLUSION

Nontuberculous mycobacterial infections cause a subacute lymphadenitis in preschool children, usually affecting the lymph nodes of the head and neck. The annual number of microbiologically confirmed cases in New Zealand had increased substantially over recent years, most notably since 1992. The reason for the increase is unknown but possible explanations include increased awareness of mycobacterial disease, external factors causing either changes in the distribution or virulence of mycobacteria in the environment and alterations in the human immune response.

摘要

目的

研究1986 - 1995年影响新西兰儿童的非结核分枝杆菌性淋巴结炎的流行病学趋势。

方法

从新西兰三个区域参考实验室的记录中识别病例。纳入所有16岁以下淋巴结组织样本非结核分枝杆菌培养呈阳性的儿童。

结果

共识别出168例病例,研究期间的前5年有43例(怀卡托地区无数据),后5年有125例。153例(91%)病例年龄在0 - 5岁组,101例(60%)为女性。头颈部是最常见的感染部位,占所有感染病例的141例(84%)。161例(96%)病例的致病病原体为鸟分枝杆菌胞内复合群。

结论

非结核分枝杆菌感染导致学龄前儿童亚急性淋巴结炎,通常累及头颈部淋巴结。近年来,新西兰微生物学确诊病例的年数量大幅增加,自1992年以来尤为显著。增加的原因尚不清楚,但可能的解释包括对分枝杆菌病的认识提高、导致环境中分枝杆菌分布或毒力变化的外部因素以及人类免疫反应的改变。

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