Német K, Szabó A, Petrányi G
Department of Epidemiology, National Institute of Haematology and Blood Transfusion, Budapest, Hungary.
Arch Immunol Ther Exp (Warsz). 1992;40(1):59-63.
Behind many clinical cases with recurrent, severe infections, absesses, delayed wound healing and especially in antibiotic resistant sepsis some granulocyte function abnormalities can be detected. The abnormalities are of inherited and acquired origin. The inherited dysfunctions are discussed here in details, but the appearance of some failures in neutrophil functions should be taken into consideration when examining patients with other diseases (e.g. diabetes, infections, periodontal disease, zinc deficiency, malignancies, uremia etc.). The main clinical tools for the diagnosis of the qualitative abnormalities in neutrophil functions are chemotaxis with migration, and an NBT test with and without stimulation, as a first indication. Any deviation in the result of these function tests requires further determinations.
在许多复发性严重感染、脓肿、伤口愈合延迟的临床病例背后,尤其是在耐抗生素败血症中,可以检测到一些粒细胞功能异常。这些异常有遗传和后天两种来源。这里详细讨论遗传性功能障碍,但在检查患有其他疾病(如糖尿病、感染、牙周病、锌缺乏、恶性肿瘤、尿毒症等)的患者时,应考虑到中性粒细胞功能出现的一些缺陷。中性粒细胞功能定性异常诊断的主要临床工具首先是趋化性迁移试验,以及有无刺激的硝基蓝四氮唑(NBT)试验。这些功能测试结果的任何偏差都需要进一步测定。