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首页> 外文期刊>The Indian journal of tuberculosis >PRIMARY TUBERCULOUS MYOSITIS: A RARE CLINICAL ENTITY
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PRIMARY TUBERCULOUS MYOSITIS: A RARE CLINICAL ENTITY

机译:原发性管肌炎:一种罕见的临床实体

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摘要

Primary tuberculous myositis without underlying pathology has been sparingly reported in medical literature. We report a case of primary tuberculous myositis of left upper arm in a seven-year-old boy. He presented with gradually increasing swelling on the medial aspect of the left arm. Ziehl Neelsen staining of pus collected revealed acid fast bacilli morphologically resembling Mycobacterium tuberculosis and the same was grown on the culture. Histopathological findings were consistent with tuberculosis. The results were confirmed by Genotype MTBDRpluse line probe assay. He was treated with standard four-drug regimen to which he responded well with complete resolution of the lesion.
机译:在医学文献中很少报道无基础病理的原发性结核性肌炎。我们报告了一例七岁男孩的左上臂原发性结核性肌炎。他表现出左臂内侧逐渐肿胀。收集的脓液的Ziehl Neelsen染色显示出耐酸性杆菌,其形态类似于结核分枝杆菌,并在培养物中生长。组织病理学发现与肺结核一致。基因型MTBDRpluse线探针测定证实了该结果。他接受了标准的四药疗法,对病灶完全缓解后对他的反应良好。

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