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我院门诊接诊一名牙龈出血患者,行血常规检查时,偶然发现患者粒细胞核形态明显异常,疑系培格尔一胡特氏家族性粒细胞核异常症。后经本省各上级医院多次检查,证实确认了这一诊断。为了准确地认识这种病症,我们复习了有关文献,并对患者家属进行了血象普查。现将检查结果加以报告,并结合文献资料,将培格尔一胡特氏家族性粒细胞核异常症的特点扼要叙述如下: 1930年,Pelger氏在二人身上首次
Outpatient clinic in our hospital admissions a gingival bleeding patients, blood routine examination, occasionally found abnormal granulocyte in patients with abnormal suspicion of the Department of Igel’s Hypertrophic familial granulocytic anomalies. After the higher level hospitals in the province several times to confirm confirmed this diagnosis. To get an accurate picture of the condition, we reviewed the literature and conducted a blood screening survey of the patients’ families. Now report the test results, combined with the literature, the characteristics of the Beagle’s Hunt’s family of familial granulocytic abnormalities briefly described as follows: In 1930, Pelger’s first time in two people